Next Article in Journal
Obesity-Induced Heart Rate Variability Impairment and Decreased Systolic Function in Obese Male Dogs
Next Article in Special Issue
Effect of Inclusion of Degraded and Non-Degraded Date Pits in Broilers’ Diet on their Intestinal Microbiota and Growth Performance
Previous Article in Journal
Beyond Glucocorticoids: Integrating Dehydroepiandrosterone (DHEA) into Animal Welfare Research
Previous Article in Special Issue
Dietary Phytogenic Combination with Hops and a Mixture of a Free Butyrate Acidifier and Gluconic Acid Maintaining the Health Status of the Gut and Performance in Chickens
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The Milk Thistle Seed Cakes and Hempseed Cakes are Potential Feed for Poultry

Department of Animal Nutrition and Forage Production, Faculty of AgriSciences, Mendel University in Brno, Zemědělská 1, CZ-613 00 Brno, Czech Republic
*
Author to whom correspondence should be addressed.
Animals 2020, 10(8), 1384; https://doi.org/10.3390/ani10081384
Submission received: 18 July 2020 / Revised: 1 August 2020 / Accepted: 6 August 2020 / Published: 10 August 2020
(This article belongs to the Collection Nutraceuticals and Animal Physiology: Performance and Welfare)

Abstract

:

Simple Summary

In accordance with Commission Regulation (EC) No 726/2004, the use of antibiotics as stimulators of animal growth and performance has been banned in all European Union countries since 2006 (due to the elimination of antibiotic residues from the human food chain). Due to this ban, many scientists are studying alternative approaches to the use of various biologically active substances with a growth-promoting effect. A promising direction is the use of alternative feeds containing bioactive compounds or mixtures of natural origin, or the use of phytoadditives or plant extracts, probiotics, prebiotics, symbiotics or oilseed by-products, such as hempseed cakes and milk thistle seed cakes, in animal nutrition.

Abstract

The aims of this work were to summarize the nutritional value of the milk thistle seed cakes and hempseed cakes and describe the influence on selected performance parameters, metabolism and animal health from inclusion of these non-traditional feeds into diets. It seems more appropriate to apply the extract of the bioactive substances complex to the livestock diets than addition of expellers or other forms of plants processing. The seed expellers, etc. mostly worsened the chickens’ performance parameters with higher doses in diets, while most of the work using the extract yields had positive results on animal performance.

1. Introduction

1.1. Silybum marianum (L.)

Silybum marianum (L.) is an annual or biennial herb naturally occurring in the regions of the Mediterranean and North Africa [1]. The active substances contained in the purple variety of milk thistle, known as the silymarin complex, have hepatoprotective, detoxifying and antioxidant effects, thanks to which parts of this plant are used for the treatment and prevention of liver and bile diseases (hepatitis, cirrhosis) and hence the protection from toxins and various chemicals substances [2].
The highest proportion of active substances of the silymarin complex is found in the seeds, which contain about 70–80% of the silymarin flavonolignans and about 20–30% of chemically undefined substances mainly of the polyphenol structure [2]. According to Kroll et al. [3] the silymarin complex is composed of at least seven flavonolignans and one flavonoid (taxifolin). Milk thistle seeds also contain betaine, trimethyl glycine and essential fatty acids involved in the hepatoprotective and anti-inflammatory effects of the silymarin complex [4,5].
Milk thistle seeds contain 23% ether extract: Oil obtained is a rich source of tocopherols and fatty acids. Milk thistle oil contains 27–64% linoleic acid (C18:2, n-6), 21–50% is oleic acid (C18:1, n-9), 7–14% palmitic acid (C16: 0) and 2–6% stearic acid (C18:0), and α-linolenic acid (C18:3, n-3) is contained in milk thistle seed oil in an amount of 5% [6].

1.2. Cannabis sativa

Hemp (Cannabis sativa L.) is an annual, up to 2 m tall plant with palm split leaves and multi-sex flowers [7]. Generally, fruits (hempseeds) contain about 25% crude protein, 30% ether extract. The gross energy content of cannabis seeds is 22 MJ/kg [8]. Unhulled hemp seeds contain 25–34% fat and dehulled seeds contain 42–47% fat. Hemp oil, obtained after the pressing of seeds, consists of 75–80% polyunsaturated fatty acids (PUFAs), of which 53–60% is linoleic acid (C18:2, n-6), 15–25% α-linolenic acid (C18:3, n-3) and 3–6% γ-linolenic acid (C18:3, n-6). Oleic acid (C18:1, n-9) contains hemp oil 8–15%. Hemp seed oil is also a rich source of tocopherols, which contains 1500 mg per kilogram [8,9]. The two major proteins present (edestin and albumin) are easily digestible and contain all essential amino acids [8,10]. In regards to protein quality, lysine is the first limiting amino acid in cannabis protein for several animals [11].
In addition to these essential nutrients, cannabis contains compounds such as plant sterols and phytocannabinoids, including the most abundant delta-9-tetrahydrocannabinol (THC), which is a strong fat-soluble antioxidant, stimulating appetite [12,13,14]. Cannabinoids are substances found only in cannabis. Cannabis contains more than 60 (phyto) cannabinoids that have anti-inflammatory, analgesic effects [15,16,17], anti-ischemic [18], antipsychotic, anxiolytic (against anxiety) [19] and effects against epilepsy [20]. Antimicrobial, immunomodulatory, antioxidant and antihypertensive effects are also described [14].
The best known and most studied of the cannabinoids is psychoactive tetrahydrocannabinol (THC), whose metabolite with potential immunosuppressive and anti-inflammatory effects that retains its psychoactive effects is cannabinol (CBN). Another metabolite of THC is the so-called cannabidiol (CBD), which no longer has psychoactive effects [21]. Other cannabinoids studied include dronabinol (DBN), nabilone, CBN, CBD, and cannabichromen (CBC) and cannabigerol (CBG). Cannabis cultivated in temperate climates contains less psychoactive cannabinoid THC, it also contains less of the second most common CBD that has no psychoactive effects [21]. The nutrient composition, and hence the composition of the cannabis ingredients and by-products, can vary considerably.
The literature points to the existence of a lipid signaling (or transmission) system (i.e., the endocannabinoid system (ECS)), which seems to significantly affect the production of reactive oxygen species, inflammation and subsequent tissue damage, and affects the body’s metabolic functions [22,23]. This system affects the immunological system [24,25] and has enormous therapeutic potential in a wide range of cancer diseases [26,27,28], pain, neurodegenerative and cardiovascular diseases up to obesity, metabolic syndrome, diabetes (diabetes mellitus) and diabetic complications [22,29].
As already mentioned, the endocannabinoid system is a central signaling receptor system affecting several biological processes. This system consists of a group of molecules known as endocannabinoids and the cannabinoid receptors to which these molecules bind [30]. Endocannabinoids are endogenous bioactive fat transporters [22]. Anandamide is one of the major endogenous cannabinoids produced by the body to date, and 2-arachidonoyl-glycerol. In addition to endocannabinoids, there are also phytocannabinoids that occur almost exclusively in cannabis seedlings and that also bind to cannabinoid receptors in the body [22,30]. Research into the endocannabinoid system has led to the discovery of two types of cannabinoid receptors—the cannabinoid-1 receptor (CB1) and the cannabinoid-2 receptor (CB2) [22]. These receptors are found in various parts of the body, but mostly in the central nervous system (CB1) and in the immune system (CB2). Both the endocannabinoids of the body and the phytocannabinoids contained in cannabis seeds fit into these cannabinoid receptors as locks. The binding of endocannabinoids or phytocannabinoids to CB1 or CB2 receptors regulates and affects physiological processes in the body and explains the wide therapeutic use of cannabis. Further research has gradually discovered endocannabinoid receptors in other organ systems of the body. In addition to the central nervous system and the immune system, the endocannabinoid system has also been discovered in the cardiovascular, gastrointestinal, genital and urinary systems [30].
Thus, the diverse physiological effects of cannabinoids are due to the existence of specific receptors distributed in some organs and systems of the body [21]. The ECS appears to play an important role in the development and control of type I diabetes. The exact mechanism of this system is still not fully discovered [22], although a hypothesis states that exogenous cannabinoids and the endo-cannabinoid system increase feed intake and improve weight gain in animals by activating central cannabinoid receptors (CB1) [29]. In addition, ECS activation has been found in obese people [31], which has led to adipogenesis, lipogenesis, hepatic steatosis and increased insulin resistance [32]. However, a mouse model has shown that a CB1 receptor antagonist is able to effectively reduce weight and thereby reduce possible metabolic risk factors [33].

2. The Seed Cakes as a Feed

2.1. Chemical Composition of Seed Cakes

For the most part, the feed quality is determined by the quality of plants. The quality of the plant and its seeds (i.e., expellers) is determined by many factors, such as agricultural technology, soil quality, climate and weather or seed treatment and seed pressing. These factors affect the crop in terms of the composition of basic nutrients as well as the composition of active substances.
Chemical composition of hempseed and milk thistle seed cakes used by us [34,35] are shown in Table 1. Generally, the seed cakes (i.e., expellers or pomace) are protein feed with residual 10% ether extract and relatively high amount of crude fiber. Figure 1 shows milk thistle seed cakes and hempseed cakes used in our experiments.
Many scientists have tried to demonstrate the effects of milk thistle in animal studies. It is believed that silymarin is mainly effective due to its anti-inflammatory and antioxidant effects, thereby stimulating hepatocyte regeneration [36]. For example, Kosina et al. [37] used milk thistle seed cakes in their experiment with rabbits containing 27% crude protein, 35% crude fiber, 10% fat, 6% starch and 4% of total flavonolignans (at 92% dry matter). This seed cakes contained more crude protein, more crude fiber and more total flavonolignans compared to ours. It was also reported [38] the following contents of the silymarin complex substances of the milk thistle seed cakes they used: 10.45 g/kg silychristin, 1.51 g/kg silydianin, 9.24 g/kg silybin A and 15.1 g/kg silybin B further 3.48 g/kg isosilybin A, 1.11 g/kg isosilybin B and 2.39 g/kg taxifolin. The contents of the substances of the silymarin complex found by the authors are much higher in comparison with ours, which could have been caused by different agricultural techniques, weather during the vegetation of the plant or by pressing the seeds themselves. In the study of Suchý et al. [39], it was stated that the milk thistle seed cakes contained 2.95% silymarin. For comparison, we present the results of Schiavone et al. [40],who used a silymarin extract containing 4.62% taxifoline, 28.21% silychristin + silydianin, 45.47% silybin isomers and 21.7% isosilybin isomers in the experiment.
Similarly, to milk thistle in animal nutrition, more scientists are studying cannabis in their work. Hemp seeds alone or in combination with hemp oil and by-products, such as seed cakes, have been included into animal diets [41,42,43,44]. In the publication of Halle and Schöne [44], hempseed cakes were used which, according to the analysis, contained (in 91% dry matter) 281 g/kg of nitrogenous substances, 110 g/kg of ether extract, 447 g/kg of neutral detergent fiber (NDF), 304 g/kg of acid-detergent fiber (ADF) and 117 g/kg of lignin. Serrapica et al. [45] determined a similar nutrient content of hempseed expellers. In contrast to the cannabinoid content, we have determined cannabidiol 170 mg/kg [34], and Halle and Schöne [44] state that the active substances content of THC and CBD was below the detection limit of 0.005%. The mineral nutrient content of hempseed cakes published by Halle and Schöne [44] is 28 g/kg calcium and 148 g/kg of phosphorus.

2.2. Seed Cakes in Broiler Diets

In our experiments, from the fattening point of view, the live weight of chickens decreased where the content of seed cakes in the mixtures increased [34,46,47,48]. The trend of the lower live weight of chickens with an increasing proportion of expellers was also confirmed in the study of Suchý et al. [39], who found that the addition of 0.2% and 1% milk thistle expellers (2% crude fiber content in diets) led to a statistically insignificant reduction in live weight and feed conversion.
On the other side, Eriksson and Wall [43], in an experiment with Ross 308 in organic mode, found a significantly higher chickens live weight (1194 g) in the experimental group with 200 g/kg of hempseed cakes compared to the control group without hempseed expellers (1071 g), at 35 days of age. According to a study by di Marzo et al. [29], exogenous cannabinoids (ingested through a diet containing cannabis products) and the endocannabinoid system increase feed intake and improve weight gain in animals by activating central cannabinoid receptors (CB1 receptor). A summary of some experiments with Milk thistle seed cakes and Hempseed cakes in animal nutrition are given in Table 2 and Table 3, respectively.
It is important to realize the seed expellers contain approx. 35% of crude fiber. High levels of fiber in poultry nutrition cause digestive disorders and due to this worsened performance. For this reason, seed expellers must be limited in feed for chickens and hens. This means low content of active substances in the poultry diets. Many studies have confirmed the trend of a decreasing live weight in chickens with increasing crude fiber content in diets. The study of Halle and Schöne [44] showed worsened performance of animals with increasing level of crude fiber in the feed mixture. In many scientific publications with the results of experiments dealing with feeding predominantly expellers (or feeding diets containing a high crude fiber content), the authors do not report the crude fiber content in poultry diets [40,43,49,55,56], although the content of this nutrient had to be increased. Therefore, it is difficult to find a recommendation for the right amount of crude fiber in poultry diets, especially when the nutrient requirements standards [57,58] do not specify a crude fiber requirement in feed mixtures. Only few publications recommend the proportion of crude fiber in mixtures for poultry. The amount of 1–4% crude fiber for young poultry is recommended [59,60]. It was recommended up to 7% of crude fiber in the diet of laying hen [61]. The technological instructions for hybrids of hens from Lohmann Tierzucht [62] state the recommended crude fiber content in feed mixtures for laying hens to be 5–6%. On the contrary, the high content of predominantly soluble part of fiber in diet poultry can cause the deterioration of performance parameters, due to slower passage of feed through the digestive tract and reduced digestibility of nutrients [63].

2.3. Seed Cakes in Hens Diets

The experiment by Št’astník et al. [35] was performed on laying hens after 69 weeks of age to investigate the possible effect of milk thistle on their livers and performance—including egg quality parameters. Perspective results are found in the addition of 7% milk thistle seed cakes in the diet of laying hens. After the sixty-ninth week of age, the laying hens in the experimental group reached a higher number of eggs and produced more egg mass compared to the control group. In the evaluation of the egg quality parameters, higher Haugh units were found, a higher millimeter height of the egg, but a thinner shell in the laying hens receiving 7% of the seed cakes. When evaluating health indicators, higher antioxidant activity was found in the experimental group [35], which could be due to silymarin content. It has a polyphenolic structure which is the reason for its antioxidant properties. The hydroxyl groups of the silymarin complex have the potential to scavenge free radicals [64]. In older laying hens, summation of the liver tissue occurs during the laying cycle due to its own high performance. The use of milk thistle seed cakes (as a source of silymarin complex) for the experiment in laying hens was chosen for potential prevention liver damage and also due to the fact a higher content of crude fiber may be included in the feed mixture of laying hens [61]. In the experiment [35], 7% of milk thistle seed cakes were added to the mixture, which meant a content of 5.3% of crude fiber in the layers’ diet.
In our experiment [35], no differences in blood biochemical parameters were found with the inclusion of 7% milk thistle (i.e., no effect of milk thistle seed cakes on the monitored parameters of liver function or other selected parameters of laying hen metabolism was found). The same conclusion was reached by Blevins et al. [65], who added 1000 mg/kg of silymarin to the feed mixture of laying hens, but found no differences in the activity of the enzymes GGT and AST, but also in the activity of cytochrome (CYP) 450 34A. On the other hand, feeding different amounts of milk thistle flour in laying hens led to a significant reduction in the triglyceride levels in the blood of the animals compared to the control group [49]. The authors Hashemi Jabali et al. [49] further found that a dose of 60 g/kg of milk thistle flour reduced the concentration of blood cholesterol, and conversely increased the concentration of HDL (high density lipoproteins) cholesterol in the blood of animals (p > 0.05). The same conclusion was reached by Suchý et al. [39], who found a significantly lower concentration of blood cholesterol in fattened chickens at the forty-third day of age after the addition of 1% milk thistle to the feed mixture. The authors Gyenis et al. [66] published a range of plasma proteins in laying hens. This range for total protein content is between 30–50 g/L and 13–28 g/L for albumin, which almost corresponds to our results [35].
In a study of Neijat et al. [42], when feeding different proportions of hemp seeds (up to 30% in the feed mixture) and hemp oil (up to 9% in the feed mixture), the performance of laying hens (feed intake, weight gain, laying and egg weight) was not affected by dietary treatments. These results are consistent with previous studies on the use of cannabis products in laying hen nutrition [53,54]. These results may indicate the effect of the endocannabinoid system on animal performance. Unfortunately, study of Neijat et al. [42] do not state the cannabinoids content of the cannabis seeds used in trial. So, the question is how many cannabinoids substances the used seeds contained and how many of it the animals received in their diet. On the other hand, in the experiment where laying hens were fed (inter alia) hempseed expellers at 5%, 10% and 15%, a significantly lower performance (feed intake, egg production and consumption egg feed) was found at a level of 15% seed cakes in diet [44]. This reduction in performance parameters (or the fact that the expellers addition did not favorably affect the performance of the laying hens) could be due to the presence of low content or absence of cannabinoids in the seed cakes. The authors mention that the hempseed expellers used by them was almost free of cannabinoids (THC and CBD were found below the detection limit of 0.005%). The hempseed cakes used in our experiments contained 0.017% CBD. Further increase in the content of seed cakes in the diets led to a reduction in the proportion of yolk and an increase in the proportion of egg white [44], for which the mentioned proteins and the quality of their amino acids could be responsible.

3. The Milk Thistle and Hemp Seed Bioactive Substances Effects on Metabolism and Performance

Many authors have tried to make milk thistle substances available to poultry without the need to feed expellers or other forms of plant by-products [40,50,67]. For example, Gawel et al. [67] fed chickens and turkeys with a commercial preparation containing 80% of silymarin at doses of 0.5 kg and 1 kg per ton of feed mixture. These authors found that the final live weight of the Cobb 500 chickens in the experimental groups was 4.8–6.6% higher than in the control group. Feed conversion ratio was balanced in all groups. The authors recorded the highest percentage of mortality (4.1%) in the chickens of the control group. Similarly, these authors Gawel et al. [67] found 1.9–3.8% higher live weight in BUT 9 hybrid turkeys fed mixtures containing the addition of silymarin compared to the control group. The turkeys were similarly affected, with a higher live weight of 2.5–3.0%. Schiavone et al. [40] found no differences in the live weight of chickens at the end of the experiment, but also in feed consumption and feed conversion when feeding a commercial milk thistle seed extract containing 40 and 80 ppm of silymarin. Another study by Zarei et al. [50] applied 1 mL of milk thistle extract in ovo in two dilutions (100 and 200 mg/L) and then also added it to the feed mixture at a dose of 100 mg/kg. They found that the level of 100 mg/L in ovo caused a significantly lower (p < 0.05) chicken’s final live weight (2125 g) at 42 days of age compared to the control group (2179 g). The feed mixture containing 100 mg/kg of extract caused significantly higher final live weight (2218 g) of chickens compared to the control group (2079 g). Silymarin also has a positive effect on feed intake, weight gain [51,68,69,70,71] and liver tissue morphology of chickens [69]. In addition, silymarin supplementation has a significant effect on meat quality and shelf life by increasing post-mortem oxidative stability [40].
The enzymes GGT and AST are considered physiological indicators of liver health. High gamma-glutamyl transferase enzyme activity in avian blood plasma is associated with hyperplasia and bile duct tumors [72]. It was claimed by Tedesco et al. [51] that silymarin content of 600 mg/kg in the diet can reduce the plasma GGT and AST activity in broiler chickens’ blood affected by aflatoxicosis. In addition, silymarin has been shown to reduce the activity of these enzymes in people with liver diseases [73] as well. In [39], significantly lowered activity of ALT and AST enzymes in the blood plasma of the experimental groups (0.2% and 1% of milk thistle seed cakes in the diets) was found, compared to the control group, on day 22 of the chicken fattening period. At day 43 of fattening, the lower activity of these enzymes in the experimental groups was not conclusive, but lower GGT enzyme activity and lower cholesterol levels were demonstrated in the group containing 1% seed cakes in the diet compared to the control group [39]. Similar results were achieved by Alassi and Allaw [74] with the addition 1 g/kg milk thistle seed powder in quail diet. A significantly lower level of cholesterol, glutathione (GSH), malondialdehyde (MDA), ALT and AST and a higher level glucose, total protein and globulin was found in the experimental group compared to the control group. Moreover, after the addition of 150 g/day of milk thistle seed cakes to dairy cattle [38], a higher AST enzyme activity was found, with other measured parameters GGT, LD, total protein, albumin, glucose, unesterified fatty acids, β-hydroxybutyrate, urea and bilirubin unchanged. In contrast to the above authors, our results in the inclusion of milk thistle seed cakes in the poultry diet did not affect the activity of liver-specific enzymes such as AST and GGT [35].
Neijat et al. [42] also found significantly lowered AST and GGT enzyme activities in laying hens with the addition of 10% and 20% of cannabis seeds into feed compared to the control group. The creatine kinase and electrolytes in the blood plasma were not affected by the experimental treatment. It might appear that the addition of cannabis seeds had a positive effect on the health of the liver tissue of the laying hens compared to the control group in the experiment [42]. The same results were achieved by Afzali et al. and Barani et al. [75,76]. On the other hand, these authors [75,76] found that groups of chickens fed a diet containing different proportions of hemp seeds and hemp seed extrudates increased the immunoglobulin G titer compared to the control group. Skřivan et al. [52] found that the dietary supplementation with 40 g/kg hempseed and 60 g/kg extruded flaxseed improved cockerel performance, meat and bone quality and deposition of alpha tocopherol in the liver. Another study, by Palade et al. [77], suggests the potential of hemp seed in sow nutrition. The diets containing 2% and 5% of hempseed improved the overall antioxidant status of the lactating sows and their progeny.
The studies with different hepatotoxic substances showed that silymarin has a multiple action as a hepatoprotective agent. Its antioxidant properties and cell regenerating functions, because of increased protein synthesis, are considered as the most important [2,78]. The bioactive complex (silymarin) can enter into the nucleus and act on RNA polymerase I enzymes and rRNA transcription, leading to increased ribosomal formation. This in turn accelerates the synthesis of protein and DNA [79] which increases the biosynthetic apparatus in the cytoplasm, thus leading to an increase in the synthesis rate of both structural and functional proteins. This stimulation may allow cells to counteract the loss of transporters and enzymes occurring under many pathological conditions. This action has important therapeutic implications in the repair of damaged hepatocytes and restoring of normal liver functions [73].
In addition, according to several studies silymarin may protect cells from oxidative (e.g., thermal) stress. The significant upregulation of oxidative stress biomarkers including MDA, TNF-like, IFN-γ and IL-1β genes was observed upon heat stress in chicken hepatocytes. Furthermore, antioxidant enzyme (superoxide dismutase, catalase, glutathione reductase) activities decreased. The silymarin (259 µM) was able to normalize the expression of all these biomarkers in heat-induced chicken hepatocytes [80]. From this, silymarin (silibinin) may upregulate and improve antioxidant defenses. In another in vitro system based on heat-induced chicken hepatocytes, silymarin (259 µM) affected heat shocks proteins (Hsp70) expression significantly, preventing its alleviation by heat stress [80]. Thus, there are many possible mechanisms by which silymarin may improve the body antioxidant defense mechanisms [81].

4. Conclusions

In the light of the above findings, it seems more appropriate to apply the extract of the bioactive substances complex to the livestock diets than addition of expellers or other forms of plants processing. The seed expellers etc. mostly worsened the chicken’s performance parameters with higher doses in diets. Therefore, it is better to include smaller proportions of these by-products in the diets of non-ruminant animals. However, most of the works using the extracts had positive results on animal performance. Although, when applying the extract to the diets, it is necessary to consider the higher costs to feed production.

Funding

This publication has been summarized with external funding of Internal Grant Agency Faculty of AgriSciences grants IP 11/2015 and TP 4/2015.

Acknowledgments

The authors gratefully thank the reviewers.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Khan, M.A.; Blackshaw, R.E.; Marwat, K.B. Biology of milk thistle (Silybum marianum) and the management options for growers in north-western Pakistan. Weed Biol. Manag. 2009, 9, 99–105. [Google Scholar] [CrossRef]
  2. Křen, V.; Walterová, D. Silybin and silymarin—New effects and applications. Biomed. Pap. 2005, 149, 29–41. [Google Scholar] [CrossRef] [Green Version]
  3. Kroll, D.J.; Shaw, H.S.; Oberlies, N.H. Milk thistle nomenclature: Why it matters in cancer research and pharmacokinetic studies. Integr. Cancer 2007, 6, 110–119. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Luper, S. A review of plants used in the treatment of liver disease: Part 1. Altern. Med. Rev. 1998, 3, 410–421. [Google Scholar] [PubMed]
  5. Saller, R.; Meier, R.; Brignoli, R. The use of silymarin in the treatment of liver diseases. Drugs 2001, 61, 2035–2063. [Google Scholar] [CrossRef] [PubMed]
  6. Chambers, C.S.; Holečková, V.; Petrásková, L.; Biedermann, D.; Valentová, K.; Buchta, M.; Křen, V. The silymarin composition and why does it matter. Food Res. Int. 2017, 100, 339–353. [Google Scholar] [CrossRef]
  7. Padua, L.S.; Bunyaprafatsara, N.; Lemmens, R.H.M.J. Medicinal and poisonous plants. In Plant Resources of South-East Asia; Valkenburg, J.L.C.H., Bunyapraphatsara, M., Eds.; Backhuys Publishers: New Delhi, India, 1999; pp. 167–175. [Google Scholar]
  8. Callaway, J.C. Hempseed as a nutritional resource: An overview. Euphytica 2004, 140, 65–72. [Google Scholar] [CrossRef]
  9. Gunstone, F.D.; Harwood, J.L. Occurence and characterisation of oils and fats. In The Lipid Handbook with CD-Rom.; Gunstone, F.D., Harwood, J.L., Dijkstra, A.J., Eds.; CRC Press: Boca Raton, FL, USA, 2007; pp. 37–141. [Google Scholar]
  10. Leizer, C.; Ribnicky, D.; Poulev, A.; Dushenkov, S.; Raskin, I. The composition of hempseed oil and its potential as an important source of nutrition. J. Nutraceuticals Funct. Med. Foods 2000, 2, 35–53. [Google Scholar] [CrossRef] [Green Version]
  11. House, J.D.; Neufeld, J.; Leson, G. Evaluating the quality of protein from hemp seed and hemp seed products through the use of the protein digestibility-corrected amino acid score method. J. Agric. Food Chem. 2010, 58, 11801–11807. [Google Scholar] [CrossRef]
  12. Hampson, A.J.; Grimaldi, M.; Lolic, M.; Wink, D.; Rosenthal, R.; Axelrod, J. Neuroprotective antioxidants from marijuana. Ann. NY Acad. Sci. 2000, 899, 274–282. [Google Scholar] [CrossRef]
  13. Koch, J.E. Delta 9-THC stimulates food intake in Lewis rats: Effects on chow, high-fat and sweet high-fat diets. Pharm. Biochem. Behav. 2001, 68, 539–543. [Google Scholar] [CrossRef]
  14. Potter, D.J.; Clark, P.; Brown, M.B. Potency of Δ9–THC and other cannabinoids in cannabis in England in 2005: Implications for psychoactivity and pharmacology. J. Forensic Sci. 2008, 53, 90–94. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Hohmann, A.G.; Suplita, R.L. Endocannabinoid mechanisms of pain modulation. Aaps. J. 2006, 8, 693–708. [Google Scholar] [CrossRef] [PubMed]
  16. Rea, K.; Roche, M.; Finn, D.P. Supraspinal modulation of pain by cannabinoids: The role of GABA and glutamate. Br. J. Pharm. 2007, 152, 633–648. [Google Scholar] [CrossRef] [Green Version]
  17. Jhaveri, M.D.; Elmes, S.J.R.; Richardson, D.; Barrett, D.A.; Kendall, D.A.; Mason, R.; Chapman, V. Evidence for a novel functional role of cannabinoid CB2 receptors in the thalamus of neuropathic rats. Eur. J. Neurosci. 2008, 27, 1722–1730. [Google Scholar] [CrossRef] [Green Version]
  18. Lamontagne, D.; Lepicier, P.; Lagneux, C.; Bouchard, J.F. The endogenous cardiac cannabinoid system: A new protective mechanism. Arch. Mal. Coeur Vaiss. 2006, 99, 242–246. [Google Scholar]
  19. Crippa, J.A.S.; Derenusson, G.N.; Ferrari, T.B.; Wichertana, L.; Duran, F.L.; Martin-Santos, R.; Filho, A.S. Neural basis of anxiolytic effects of cannabidiol (CBD) in generalized social anxiety disorder: A preliminary report. J. Psychopharmacol. 2011, 25, 121–130. [Google Scholar] [CrossRef]
  20. Mortati, K.; Dworetzky, B.; Devinsky, O. Marijuana: An effective antiepileptic treatment in partial epilepsy? A case report and review of the literature. Rev. Neurol. Dis. 2007, 4, 103–106. [Google Scholar]
  21. Alvarado, R.I.N.; Sánchez, R.M.; Del, C.; Salcedo, V.V. Therapeutic properties of cannabinoid drugs and marijuana in several disorders: A narrative review. Salud. Ment. 2017, 40, 111–118. [Google Scholar] [CrossRef] [Green Version]
  22. Horváth, B.; Mukhopadhyay, P.; Haskó, G.; Pacher, P. The endocannabinoid system and plant derived cannabinoids in diabetes and diabetic complications. Am. J. Pathol. 2012, 180, 432–442. [Google Scholar] [CrossRef] [Green Version]
  23. Silver, R. The endocannabinoid system of animals. Animals 2019, 9, 686. [Google Scholar] [CrossRef] [Green Version]
  24. Malek, T.R. The biology of interleukin-2. Ann. Rev. Immunol. 2008, 26, 453–479. [Google Scholar] [CrossRef] [PubMed]
  25. Bihl, F.; Germain, C.; Luci, C.; Braud, V.M. Mechanisms of NK cell activation: CD4+ T cells enter the scene. Cell. Mol. Life Sci. 2011, 68, 3457–3467. [Google Scholar] [CrossRef] [PubMed]
  26. Hermanson, D.J.; Marnett, L.J. Cannabinoids, endocannabinoids, and cancer. Cancer Metastasis Rev. 2011, 30, 599–612. [Google Scholar] [CrossRef] [PubMed]
  27. Sarfaraz, S.; Adhami, V.M.; Syed, D.N.; Afaq, F.; Mukhtar, H. Cannabinoids for cancer treatment: Progress and promise. Cancer Res. 2008, 68, 339–342. [Google Scholar] [CrossRef] [Green Version]
  28. Mcalliste, S.D.; Rigel, T.C.; Horowitz, M.P.; Garcia, A.; Desprez, P.Y. Cannabidiol as a novel inhibitor of Id-1 gene expression in aggressive breast cancer cells. Mol. Cancer 2007, 6, 2921–2927. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Di Marzo, V.; Piscitelli, F.; Mechoulam, R. Cannabinoids and endocannabinoids in metabolic disorders with focus on diabetes. In Diabetes—Perspectives in Drug Therapy; Schwanstecher, M., Ed.; Springer: Berlin, Germany, 2011; pp. 75–104. [Google Scholar]
  30. Aizpurua-Olaizola, O.; Elezgarai, I.; Rico-Barrio, I.; Zarandona, I.; Etxebarria, N.; Usobiaga, A. Targeting the endocannabinoid system: Future therapeutic strategies. Drug. Discov. Today 2017, 22, 105–110. [Google Scholar] [CrossRef] [PubMed]
  31. Engeli, S.; Bohnke, J.; Feldpausch, M.; Gorzelniak, K.; Janke, J.; Batkai, S.; Pacher, P.; Harvey-White, J.; Luft, F.C.; Sharma, A.M.; et al. Activation of the peripheral endocannabinoid system in human obesity. Diabetes 2005, 54, 2838–2843. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Di Marzo, V. The endocannabinoid system in obesity and type 2 diabetes. Diabetologia 2008, 51, 1356–1367. [Google Scholar] [CrossRef] [Green Version]
  33. Tam, J.; Vemuri, V.K.; Liu, J.; Bátkai, S.; Mukhopadhyay, B.; Godlewski, G.; Osei-Hyiaman, D.; Ohnuma, S.; Ambudkar, S.V.; Pickel, J.; et al. Peripheral CB1 cannabinoid receptor blockade improves cardiometabolic risk in mouse models of obesity. J. Clin. Invest. 2010, 120, 2953–2966. [Google Scholar] [CrossRef] [Green Version]
  34. Šťastník, O.; Jůzl, M.; Karásek, F.; Fernandová, D.; Mrkvicová, E.; Pavlata, L.; Nedomová, Š.; Vyhnánek, T.; Trojan, V.; Doležal, P. The effect of hempseed expellers on selected quality indicators of broiler chicken’s meat. Acta Vet. Brno 2019, 88, 121–128. [Google Scholar] [CrossRef] [Green Version]
  35. Šťastník, O.; Mrkvicová, E.; Pavlata, L.; Roztočilová, A.; Umlášková, B.; Anzenbacherová, E. Performance, biochemical profile and antioxidant activity of hens supplemented with addition of milk thistle (Silybum marianum) seed cakes in diet. Acta Univ. Agric. Silvc. Mendel. Brun. 2019, 67, 993–1003. [Google Scholar] [CrossRef] [Green Version]
  36. Vargas-Mendoza, N.; Madrigal-Santillán, E.; Morales-González, A.; Esquivel-Soto, J.; Esquivel-Chirino, C.; García-Luna, Y.; González-Rubio, M.; Gayosso-De-Lucio, J.A.; Morales-González, J.A. Hepatoprotective effect of silymarin. World J. Hepatol. 2014, 6, 144–149. [Google Scholar] [CrossRef] [PubMed]
  37. Kosina, P.; Dokoupilová, A.; Janda, K.; Sládková, K.; Silberová, P.; Pivodová, V.; Ulrichová, J. Effect of Silybum marianum fruit constituents on the health status of rabbits in repeated 42 day fattening experiment. Anim. Feed Sci. Tech. 2017, 223, 128–140. [Google Scholar] [CrossRef]
  38. Křížová, L.; Watzková, J.; Třináctý, J.; Richter, M.; Buchta, M. Rumen degradability and whole tract digestibility of flavonolignans from milk thistle (Silybum marianum) fruit expeller in dairy cows. Czech J. Anim. Sci. 2011, 56, 269–278. [Google Scholar] [CrossRef] [Green Version]
  39. Suchý, P.; Straková, E.; Kummer, V.; Herzig, I.; Písaříková, V.; Blechová, R.; Mašková, J. Hepatoprotective effects of milk thistle (Silybum marianum) seed cakes during the chicken broiler fattening. Acta Vet. Brno 2008, 77, 31–38. [Google Scholar] [CrossRef] [Green Version]
  40. Schiavone, A.; Righi, F.; Quarantelli, A.; Bruni, R.; Serventi, P.; Fusari, A. Use of Silybum marianum fruit extract in broiler chicken nutrition: Influence on performance and meat quality. J. Anim. Physiol. Nutr. 2007, 91, 256–262. [Google Scholar] [CrossRef]
  41. Khan, U.R.; Durrani, F.R.; Chand, N.; Anwar, H. Influence of feed supplementation with cannabis sativa on quality of broilers carcass. Pak. Vet. J. 2010, 30, 34–38. [Google Scholar]
  42. Neijat, M.; Gakhar, N.; Neufeld, J.; House, J.D. Performance, egg quality, and blood plasma chemistry of laying hens fed hempseed and hempseed oil. Poult. Sci. 2014, 93, 2827–2840. [Google Scholar] [CrossRef]
  43. Eriksson, M.; Wall, H. Hemp seed cake in organic broiler diets. Anim. Feed Sci. Tech. 2012, 171, 205–213. [Google Scholar] [CrossRef]
  44. Halle, I.; Schöne, F. Influence of rapeseed cake, linseed cake and hemp seed cake on laying performance of hens and fatty acid composition of egg yolk. J. Verbrauch Lebensm 2013, 8, 185–193. [Google Scholar] [CrossRef]
  45. Serrapica, F.; Masucci, F.; Raffrenato, E.; Sannino, M.; Vastolo, A.; Barone, C.; Di Francia, A. High fiber cakes from mediterranean multipurpose oilseeds as protein sources for ruminants. Animals 2019, 9, 918. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Šťastník, O.; Jůzl, M.; Karásek, F.; Štenclová, H.; Nedomová, Š.; Pavlata, L.; Mrkvicová, E.; Doležal, P.; Jarošová, A. The effect of feeding milk thistle seed cakes on quality indicators of broiler chickens meat. Potravinarstvo 2016, 10, 248–254. [Google Scholar] [CrossRef] [Green Version]
  47. Stastnik, O.; Karasek, F.; Stenclova, H.; Trojan, V.; Vyhnanek, T.; Pavlata, L.; Mrkvicova, E. The effect of hempseed cakes on broiler chickens peroformance parameters. In Proceedings of the 22nd International PhD Students Conference Location, Mendel University, Brno, Czech Republic, 11–12 November 2015; pp. 157–160. [Google Scholar]
  48. Stastnik, O.; Detvanova, L.; Karasek, F.; Stenclova, H.; Kalhotka, L.; Pavlata, L.; Mrkvicova, E. The Influence of Milk Thistle Seed Cakes on Broiler Chickens Performance Parameters. In Proceedings of the 22nd International PhD Students Conference Location, Mendel University, Brno, Czech Republic, 11–12 November 2015; pp. 152–156. [Google Scholar]
  49. Hashemi Jabali, N.S.; Mahdavi, A.H.; Ansari Mahyari, S.; Sedghi, M.; Akbari Moghaddam Kakhki, R. Effects of milk thistle meal on performance, ileal bacterial enumeration, jejunal morphology and blood lipid peroxidation in laying hens fed diets with different levels of metabolizable energy. J. Anim. Physiol. N 2017, 101, 1–11. [Google Scholar] [CrossRef] [PubMed]
  50. Zarei, A.; Morovat, M.; Chamani, M.; Sadeghi, A.A.; Dadvar, P. Effect of in ovo feeding and dietary feeding of Silybum marianum extract on performance, immunity and blood cation anion balance of broiler chickens exposed to high temperatures. Iran. J. Appl. Anim. Sci. 2016, 6, 697–705. [Google Scholar]
  51. Tedesco, D.; Steidler, S.; Galletti, S.; Tameni, M.; Sonzogni, O.; Ravarotto, L. Efficacy of silymarin-phospholipid complex in reducing the toxicity of aflatoxin B1 in broiler chickens. Poult. Sci. 2004, 83, 1839–1843. [Google Scholar] [CrossRef]
  52. Skřivan, M.; Englmaierová, M.; Taubner, T.; Skřivanová, E. Effects of dietary hemp seed and flaxseed on growth performance, meat fatty acid compositions, liver tocopherol concentration and bone strength of cockerels. Animals 2020, 10, 458. [Google Scholar] [CrossRef] [Green Version]
  53. Silversides, F.G.; Lefrancois, M.R. The effect of feeding hemp seed meal to laying hens. Br. Poult. Sci. 2005, 46, 231–235. [Google Scholar] [CrossRef]
  54. Gakhar, N.; Goldberg, E.; Jing, M.; Gibson, R.; House, J.D. Effect of feeding hemp seed and hemp seed oil on laying hen performance and egg yolk fatty acid content: Evidence of their safety and efficacy for laying hen diets. Poult. Sci. 2012, 91, 701–711. [Google Scholar] [CrossRef]
  55. Kalantar, M.; Salary, J.; Sanami, M.N.; Khojastekey, M.; Matin, H.R.H. Dietary supplementation of Silybum marianum or curcuma spp on health characteristics and broiler chicken performance. Glob. J. Anim. Sci. Res. 2014, 2, 58–63. [Google Scholar]
  56. Lichovnikova, M.; Kalhotka, L.; Adam, V.; Klejdus, B.; Anderle, V. The effects of red grape pomace inclusion in grower diet on amino acid digestibility, intestinal microflora, and sera and liver antioxidant activity in broilers. Turk. J. Vet. Anim. Sci. 2015, 39, 406–412. [Google Scholar] [CrossRef]
  57. National Research Council. Nutrient Requirements of Poultry; National Academy Press: Washington, DC, USA, 1994. [Google Scholar]
  58. Aviagen Group. Broiler Nutrition Specifications. Available online: http://en.aviagen.com/ross-308 (accessed on 20 May 2020).
  59. González-Alvarado, J.M.; Jiménez-Moreno, E.; Lázaro, R.; Mateos, G.G. Effect of type of cereal, heat processing of the cereal, and inclusion of fiber in the diet on productive performance and digestive traits of broilers. Poult. Sci. 2007, 86, 1705–1715. [Google Scholar] [CrossRef] [PubMed]
  60. Mateos, G.G.; Jimenez-Moreno, E.; Serrano, M.P.; Lazaro, R.P. Poultry response to high levels of dietary fiber sources varying in physical and chemical characteristics. J. Appl Poult. Res. 2012, 21, 156–174. [Google Scholar] [CrossRef]
  61. Albiker, D.; Bieler, R.; Zweifel, R. Crude fibre in layer feed influences performance and plumage of LSL Hybrid. In Proceedings of the 20th European Symposium on Poultry Nutrition (ESPN), Prague, Czech Republic, 24–27 August 2015. [Google Scholar]
  62. Lohmann Tierczucht. Management Guide. Available online: http://www.ltz.de/en/downloads/management-guides.php#anchor_0955c6a8_Accordion-1-Cage (accessed on 20 May 2020).
  63. Honzík, Z. Vláknina ve výživě nosnic: Význam výběru správného zdroje vlákniny. Drůbežář 2015, 2, 18–20. [Google Scholar]
  64. Miranda, C.L.; Stevens, J.F.; Ivanov, V.; Mccall, M.; Frei, B.; Deinzer, M.L.; Buhler, D.R. Antioxidant and prooxidant actions of prenylated and nonprenylated chalcones and flavanones in vitro. J. Agric. Food Chem. 2000, 48, 3876–3884. [Google Scholar] [CrossRef]
  65. Blevins, S.; Siegel, P.; Blodgett, D.; Ehrich, M.; Saunders, G.; Lewis, R. Effects of silymarin on gossypol toxicosis in divergent lines of chickens. Poult. Sci. 2010, 89, 1878–1886. [Google Scholar] [CrossRef]
  66. Gyenis, J.; Suto, Z.; Romvari, R.; Horn, P. Tracking the development of serum biochemical parameters in two laying hen strains—A comparative study. Arch. Tierz. 2006, 49, 593–606. [Google Scholar] [CrossRef]
  67. Gawel, A.; Kotonski, B.; Madej, J.; Mazurkiewicz, M. Effect of silimarin on chicken and turkey broilers’ rearing and the production indices of reproduction hen flocks. Med. Weter 2003, 59, 517–520. [Google Scholar]
  68. Schönfeld, J.V.; Weisbrod, B.; Müller, M. Silibinin, a plant extract with antioxidant and membrane stabilizing properties, protects exocrine pancreas from cyclosporin A toxicity. Cell. Mol. Life Sci. 1997, 53, 917–920. [Google Scholar] [CrossRef]
  69. Gažák, R.; Walterová, D.; Křen, V. Silybin and silymarin-new and emerging applications in medicine. Curr. Med. Chem. 2007, 14, 315–338. [Google Scholar] [CrossRef]
  70. Chand, N.; Din Muhammad, F.R.; Durrani, M.; Sahibzada, S. Protective effects of milk thistle (Silybum marianum) against aflatoxin B1 in broiler chicks. Asian Austral. J. Anim. 2011, 24, 1011–1018. [Google Scholar] [CrossRef]
  71. Makki, O.F.; Afzali, N.; Omidi, A. Effect of different levels of Silymarin (Silybum marianum) on growth rate, carcass variables and liver morphology of broiler chickens contaminated with aflatoxin B1. Poult. Sci. J. 2013, 1, 105–116. [Google Scholar]
  72. Harr, K.E. Clinical chemistry of companion avian species: A review. Vet. Clin. Pathol 2002, 31, 140–151. [Google Scholar] [CrossRef] [PubMed]
  73. Wellington, K.; Jarvis, B. Silymarin: A review of its clinical properties in the management of hepatic disorder. BioDrugs 2001, 15, 465–489. [Google Scholar] [CrossRef]
  74. Alassi, S.B.; Allaw, A.A. Effect of adding of the milk thistle (Silybum marianum) seed powder in the traits of biochemical blood of the quail. Plant. Arch. 2020, 20, 962–964. [Google Scholar]
  75. Afzali, N.; Barani, M.; Hosseini Vashan, S.J. The effect of different levels of extruded hempseed (Cannabis sativa L.) on performance, plasma lipid profile and immune response of broiler chicks. In Proceedings of the 20th European Symposium on Poultry Nutrition (ESPN), Prague, Czech Republic, 24–27 August 2015; p. 196. [Google Scholar]
  76. Barani, M.; Afzali, N.; Hosseini Vashan, S.J. The effect of hempseed (Cannabis sativa L.) on performance, some blood biochemical parameters and immune response of broiler chickens. In Proceedings of the 20th European Symposium on Poultry Nutrition (ESPN), Prague, Czech Republic, 24–27 August 2015; p. 198. [Google Scholar]
  77. Palade, L.; Habeanu, M.; Marin, D.; Chedea, V.; Pistol, G.; Grosu, I.; Gheorghe, A.; Ropota, M.; Taranu, I. Effect of dietary hemp seed on oxidative status in sows during late gestation and lactation and their offspring. Animals 2019, 9, 194. [Google Scholar] [CrossRef] [Green Version]
  78. Kosina, P.; Maurel, P.; Ulrichova, J.; Dvorak, Z. Effect of silybin and its glycosides on the expression of cytochromes P450 1A2 and 3A4 in primary cultures of human hepatocytes. J. Biochem. Mol. Toxicol. 2005, 19, 149–153. [Google Scholar] [CrossRef]
  79. Sonnenbichler, J.; Zetl, I. Biochemical effects of the flavonolignane silibinin on RNA, protein and DNA synthesis in rat livers. Prog. Clin. Biol. Res. 1986, 213, 319–331. [Google Scholar]
  80. Oskoueian, E.; Abdullah, N.; Idrus, Z.; Ebrahimi, M.; Goh, Y.M.; Shakeri, M.; Oskoueian, A. Palm kernel cake extract exerts hepatoprotective activity in heat-induced oxidative stress in chicken hepatocytes. BMC Complement. Altern. Med. 2014, 14, 368. [Google Scholar] [CrossRef] [Green Version]
  81. Surai, P.F. Silymarin as a natural antioxidant: An overview of the current evidence and perspectives. Antioxidants 2015, 4, 204–247. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Seed cakes: (a) Milk thistle seed cakes are produced by seeds pressed through a hydraulic press; (b) hempseed cakes are formed by seeds extruded through a screw press.
Figure 1. Seed cakes: (a) Milk thistle seed cakes are produced by seeds pressed through a hydraulic press; (b) hempseed cakes are formed by seeds extruded through a screw press.
Animals 10 01384 g001
Table 1. Seed cakes chemical composition (dry matter basis).
Table 1. Seed cakes chemical composition (dry matter basis).
NutrientMilk Thistle Seed CakesHempseed Cakes
Gross energy (MJ/kg)20.30 [35]20.40 *
Crude protein (g/kg)217.00 [35]298.04 [34]
Ether extract (g/kg)100.70 [35]96.94 [34]
Crude ash (g/kg)68.00 [35]72.46 [34]
Crude fiber (g/kg)292.40 [35]325.53 [34]
ADF (g/kg)413.80 [35]420.64 *
NDF (g/kg)455.40 [35]478.11 *
β-carotene (mg/kg)6.47 *18.72 [34]
Cyanidine-3-glucoside (mg/kg)129.83 *46,62 [34]
Cannabidiol (mg/kg)-170 [34]
Tetrahydrocannabinol-non-detectable
Cannabinol-non-detectable
Taxifolin (mg/kg)580 [35]-
Silychristin (mg/kg)3638 [35]-
Silydianin (mg/kg)2520 [35]-
Silybin B (mg/kg)6673 [35]-
Silybin A (mg/kg)1473 [35]-
Isosilybin (mg/kg)565 [35]-
* results from our analysis (unpublished data); ADF—acid-detergent fiber; NDF—neutral detergent fiber
Table 2. The milk thistle seed cakes in poultry diets.
Table 2. The milk thistle seed cakes in poultry diets.
AnimalsExp. DurationType and Dose of AdditiveActive Substances ConcentrationMain EffectRef.
Speciesn
Hens, Bovans Brown3011 weeks (77 days)Milk thistle seed cakes at 7%Flavonolignans 37.3 mg/kghigher number of eggs, more egg mass, higher antioxidant activity in the experimental group.[35]
Rabbits, HYLA36042 daysSilybum marianum fruit 0.2% or 1%Flavonolignans 4%Mild effect on performance parameters.[37]
Holstein cows313 daysMilk thistle fruit expeller at 150 g/day/cow4.10 ± 0.10 mass percentage of the silymarin complexAnimals receiving the milk thistle expeller had a higher content of plasma conjugated silybin.[38]
Broiler chickens, ROSS 30818022, 43 and 52 daysSilybum marianum seed cakes 0.2% or 1%2.95% of silymarinLower cholesterol, AST, ALT in exp. Groups.[39]
Broiler chickens, ROSS 50818060 days40 ppm and 80 ppm of a silymarinTaxifolin—4.65%; Silychristin + Silydianin—28.21%;
Silybin isomers—45.47%;
Isosilybin isomers—21.7%
Silymarin at the tested doses did not affect growth performances but slightly affected slaughtering yields negatively.[40]
Broiler chickens, ROSS 30815025 daysMilk thistle seed cakes at 5% and 15%Flavonolignans 37.3 mg/kgThe milk thistle seed cakes do not worsen the sensory characteristic of breast or thigh meat of broilers and reflects optimal sensory quality traits.[46]
Leghorn hens, Hy-Line W-3620070 daysMilk thistle meal 15%, 30%, 60%470.64 mg gallic acid equivalent/g of the sampleMilk thistle meal has antioxidant effect, beneficial effects on ileal pathogenic bacteria, intestinal histological alterations and production and reduction of serum MDA[49]
Broiler chickens, ROSS 308360 eggs and 240 chickens1–21 days and 22–42 days100 mg/L and 200 mg/L in ovo and (or) 100 mg/kg of Silybum marianum extract in dietSilymarin (≥80%) and Silybin isomers (≥30%)Dietary feeding of the extract to broiler chickens increased immunity response under elevated temperatures, but in ovo feeding of the extract had no impact on immunity.[50]
Broiler chickens2135 daysAflatoxin B1 at 0.8 mg/kg of feed + silymarin phytosome at 600 mg/kgSilymarin phytosomeSilymarin might be used in chickens to prevent the effects of aflatoxin B1 in contaminated feed.[51]
Exp.—experiment; Ref.—references.
Table 3. The hempseed cakes in poultry diets.
Table 3. The hempseed cakes in poultry diets.
AnimalsExp. DurationType and Dose of AdditiveActive Substances ConcentrationMain EffectRef.
Speciesn
Broiler chickens, ROSS 30815025 daysHempseed cakes 5% and 15%170 mg/kg of CBDHempseed cakes affect the colour and odor of broiler chicken’s meat, which is positive for the consumers.[34]
Lohmann LSL-Classic4812 weeks (84 days)Hempseed 10%, 20% or 30%; hempseed oil 4.5% or 9%Only nutrient compositionHempseed and hempseed oil are tolerated by hens and may suggest protective effect in liver damage.[42]
Broiler chickens, ROSS 308120070 daysHempseed cake 100 and 200 g/kgAverage level of THC (1–1.5 g/kg dry weight)It was not affected total performance parameters, mortality or microbiological measures.[43]
Laying hens216168 daysHempseed cake 50, 100 or 150 g/kgThe THC and CBD content was below the detection limit of 0.005%.Up to 10% of hempseed cake do not negatively influenced the laying hens performance and provide the possibility of the enrichment of yolk fat with n-3 type PUFA.[44]
Broiler chickens, ROSS 30854035 daysHempseed 30, 40 and 50 g/kg in dietsOnly nutrient and fatty acids compositionHempseed in diet increases tibia strength. The dietary supplementation with 40 g/kg hempseed and 60 g/kg extruded flaxseed improves bird’s performance, meat and bone quality and deposition of α-tocopherol in the liver.[52]
Hens, DeKalb1024 weeks(28 days)Hempseed meal 50, 100 and 200 g/kgOnly nutrient contentNo differences were found for egg production, feed consumption, feed conversion ratio, body weight or egg quality.[53]
Hens, Bovans White4812 weeks(84 days)Hempseed oil 4%, 8% and 12%; Hempseed 10% and 20%Only nutrient and fatty acids compositionUp to a maximum level of 20% hempseeds and 12% hempseed oil does not affect laying hens’ performance and leads to the enrichment of the n-3 fatty acid content of eggs.[54]
Exp.—experiment; Ref.—references; PUFA—polyunsaturated fatty acids.

Share and Cite

MDPI and ACS Style

Stastnik, O.; Pavlata, L.; Mrkvicova, E. The Milk Thistle Seed Cakes and Hempseed Cakes are Potential Feed for Poultry. Animals 2020, 10, 1384. https://doi.org/10.3390/ani10081384

AMA Style

Stastnik O, Pavlata L, Mrkvicova E. The Milk Thistle Seed Cakes and Hempseed Cakes are Potential Feed for Poultry. Animals. 2020; 10(8):1384. https://doi.org/10.3390/ani10081384

Chicago/Turabian Style

Stastnik, Ondrej, Leos Pavlata, and Eva Mrkvicova. 2020. "The Milk Thistle Seed Cakes and Hempseed Cakes are Potential Feed for Poultry" Animals 10, no. 8: 1384. https://doi.org/10.3390/ani10081384

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop