Basic Research Open Access
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 15, 2003; 9(3): 553-556
Published online Mar 15, 2003. doi: 10.3748/wjg.v9.i3.553
Significance of changes of gastrointestinal peptides in blood and ileum of experimental spleen deficiency rats
Li-Sheng Li, Rui-Yao Qu, Wei Wang, Hua Guo, Department of Physiology, Capital University of Medical Sciences, 100054, Beijing, China
Author contributions: All authors contributed equally to the work.
Supported by the Traditional Chinese Medicine-Drug Science and Technology Development Foundation, Beijing City (1999-2000)
Correspondence to: Li-Sheng Li, Department of Physiology, Capital University of Medical Sciences, 100054, Beijing, China. lls@sohu.com
Telephone: +86-10-63051492
Received: September 13, 2002
Revised: October 15, 2002
Accepted: October 31, 2002
Published online: March 15, 2003

Abstract

AIM: To explore the mechanism of spleen deficiency (SD) by studying the relationship of gastro-intestinal peptides level and ileal electro-mechanical activity of SD rats and cold restrain rats.

METHODS: (1) spleen deficiency (SD) model was established by feeding Houpou:Zhishi: Dahuang in the ratio of 3:3:2, 3 ml/time, for 42 days. (2) The cold restrain stress model: Animals were restrained on grille and placed in a cool water at 18 °C for 3 h. (3) Substance P (SP) and vasoactive intestinal peptide (VIP) levels in all layers of initial part of ileum and blood in rats were measured by radioimmunoassays (RIA) while changes of electric activity and motility in ileum of rats were recorded with electrode and strain gauge.

RESULTS: SP levels in ileum and blood of experimental SD rats were significantly higher than that of the control groups (9.89 ± 5.65 vs 1.22 ± 1.18, P < 0.005, in ileum; 22.7 ± 3.95 vs 6.60 ± 1.47, P < 0.001, in blood) while the VIP levels of the SD rats were significantly lower than that of the controls (3.50 ± 2.01 vs 9.10 ± 4.91, P < 0.05, in ileum; 229.8 ± 62.4 vs 560.4 ± 151.3, P < 0.001, in blood). As compared with the controls, the average frequency of slow electric waves (21.3 ± 0.96 vs 18.2 ± 2.28, P < 0.05) and motility (21.5 ± 0.58 vs 18 ± 2.65, P < 0.005) of SD rats increased obviously and the frequency of fast waves of SD rat also increased. In spontaneous recovery cases, SP levels recovered significantly (compared with the SD groups, 2.99 ± 0.62 vs 9.89 ± 5.65, P < 0.001, in ileum; 14.4 ± 4.22 vs 22.7 ± 3.95, P < 0.001, in blood) but did not drop to normal. After the SD rats treated with Chinese herbs (Jiawei Sijun zi Tang), SP improved (compared with SD cases, 2.20 ± 1.25 vs 9.89 ± 5.65, (P < 0.001), in ileum; 10.7 ± 1.88 vs 22.7 ± 3.95, (P < 0.001), in blood) and VIP in blood also improved (compared with SD rats, 485.7 ± 229.0 vs 229.8 ± 62.4, P < 0.01) while the amplitude of motility decreased apparently (compared with the SD rats, 0.64 ± 0.096 vs 0.89 ± 0.15, P < 0.01). The ileal SP levels of cool stress didn’t change while the ileal VIP levels of cool stress became significantly lower than that of the control groups (2.87 ± 0.87 vs 9.10 ± 4.91, P < 0.01). The blood SP levels of cool stress were significantly higher (15.60 ± 1.83 vs 6.60 ± 1.47, P < 0.001) whereas the blood VIP levels of cool stress were significantly lower than that of the control group (153.4 ± 70.46 vs 560.4 ± 151.30, P < 0.001).

CONCLUSION: Changes of SP and VIP levels in initial part of ileum and blood of SD rats and cool stress rats may be closely related to the gastrointestinal motility disorders presented in SD and cool stress rats. the Chinese herbs (Jiawei Sijun zi Tang) currently used have partially therapeutic effect.




INTRODUCTION

It was well known that Spleen-Stomach theory is an important constituent of the theoretical basis of traditional Chinese Medicine. The spleen here is not synonymous with the spleen in western medicine anatomically, physiologically or pathophysiologically[1-3]. Conceptually, Spleen-Stomach theory is a comprehensive one. It mainly involves the digestive system, its vegetative nervous system, immunologic function, hemopoiesis, muscle metabolism, endocrine function, hepatic metabolic function, protein, nucleotide, energy, water and salt metabolism.

In recent years, the field of gastrointestinal hormones has expanded at a dazzling speed. The successful isolation of some gastrointestinal hormones and development of sensitive assays for their detection have led to many unexpected findings[4]. Gastrointestinal hormones as regulatory peptides appear to be major components of bodily integration and have important regulatory actions on physiological function of gastrointestinal tract[5-17]. Some studies indicated that spleen deficiency syndrome (SDS) was closely related with gastrointestinal hormones[18-21].

But up to now, the mechanisms of the relationship between gastrointestinal peptides levels and gastrointestinal functional disorder in SD still remain unclear[22-31]. We tried to explore the relationship between SDS and gastrointestinal hormones by measuring SP and VIP, and by using electrode and highly sensitive strain sensor to record alterations of ileum activity and ileum motility in SD and cool stress rats.

MATERIALS AND METHODS
Experimental animals

Healthy adult male Wistar rats (provided by Experimental Animal center, capital university of medical sciences), weighing 0.12-0.17 kg were used in this study. They were caged in an air conditioned room (23 + 2 °C).

Sijunzi decoction (SJZD), composed of ginseng, Atractylodes, Poria, Glycyrrhiza, It was prepared by routine method of decocting the crude herbal medicine twice. The filtered medication was preserved in refrigerator at 4 °C.

Fifty rats were randomly divided into five groups: (1) control group: The rats were fed standard rat chow and water ad labium. (2) experimental SD model group. by feeding Houpou: Zhishi: Dahuang (3:3:2), 3 ml/time, 42 day. (3) Spontaneous recovery group. (4) SJZD treated group. (5) cold stress group: rats were restrained on grille and placed in cool water at 18 °C for 3 h.

Measurements

Radioimmunoassay (RIA) of SP and VIP in these samples was conducted with kits purchased from Beijing HaiKerui Biological technique center. The concentrations of SP, VIP were measured with radioimmunoassay kits. Under anesthesia, the abdomen was opened and the samples were taken as follows: (1) Blood samples of 5-6 ml from the heart were collected in tubes, the plasma was immediately separated by centrifugation, then was frozen and stored at -20 °C until analysis. (2) The initial part of ileal tissue were removed, rinsed and weighed, then were put into a tube with boiling water. The tube was plunged into vigorous boiling water for 3 minutes, then it was cooled down and homogenized for 10 minutes. After centrifugation at 3000 r/min for 5 minutes, the supernatant was collected and stored at -20 °C until assay.

All groups fasted for 18 h before operating, anesthetized by 20% urethane, the abdomen was opened, then the sliver electrodes and strain gauge were implanted on the initial part of ileum. The changes of electric slow wave and motility of ileum were recorded. Electrode wires were passed through the abdominal muscle and fixed on the skin. All data were handled by a two-channel physiological recorder and a computer.

The cold restrain stress model: Animals were restrained on grille and placed in a cool water at 18 °C for 3 h.

Statistical analysis

Data were expressed as mean ± standard deviation. Experimental results were analyzed by t tests was determined P < 0.05 was considered statistically significant.

RESULTS

To assess the changes of gut peptides of gastrointestinal functional disorder in SD rats and cold restraint rats, we measured the plasma levels of SP and VIP and those in the initial part of the ileum. SP levels in ileum and blood of experimental SD rats were significantly higher than those of the control groups (P < 0.005, in ileum; P < 0.001, in blood) while the VIP levels of the SD rats were significantly lower than those of the controls (P < 0.05 in Ileum, P < 0.001, in blood). In spontaneous recovery cases, SP levels recovered significantly (compared with the SD groups, P < 0.001) and did not drop to normal. After the SD rats were treated with Chinese herbs (Jiawei Sijun Zi Tang), SP was improved (compared with SD cases, P < 0.001) and VIP in blood was also improved (compared with SD rats, P < 0.01. SP levels in ileum of cool stress didn’t change while the VIP levels were significantly lower than that of the controls groups (P < 0.01). SP levels in blood of cool stress were significantly higher (P < 0.001) while the VIP levels were significantly lower than that of the control groups (P < 0.001), Table 1 and Table 2.

Table 1 Changes of SP and VIP in plasma (-x± s, µg·L-1).
GroupnSPVIP
Control group76.60 ± 1.47560.40 ± 151.30
SD group822.7 ± 3.95a229.8 ± 62.4a
Spontaneous recovery group714.4 ± 4.22c332.7 ± 119.1
Treated group710.7 ± 1.88b485.7 ± 229.0c
Cool stress group715.60 ± 1.83a153.4 ± 70.46a
Table 2 Changes of SP and VIP in ileum (WB/ρg·mg-1. -x±s).
GroupnSPVIP
Control group71.22 ± 1.189.10 ± 4.91
SD group89.89 ± 5.65a3.50 ± 2.01c
Spontaneous recovery group72.99 ± 0.62b4.11 ± 0.83
Treated group72.20 ± 1.25b4.48 ± 1.14
Cool stress group70.57 ± 0.512.87 ± 0.87c

As compared with the controls, average frequency of slow electric waves (P < 0.05) and motility (P < 0.05) of SD rats increased obviously while the amplitude of motility decreased apparently (P < 0.05), Table 3.

Table 3 Changes of electric-mechanical activity in ileum (-x±s).
Main frequency (time/min)
Average frequency (time/min )
Amplitude (time/min )
Slow waveMotilitySlow waveMotilitySlow waveMotility
Control group17.5 ± 2.0518.5 ± 1.718.2 ± 2.2818 ± 2.650.30 ± 0.260.43 ± 0.31
SD group17.4 ± 0.7918.0 ± 0.6921.3 ± 0.96b21.5 ± 0.58a0.31 ± 0.240.89 ± 0.15b
Spontaneous recovery group16.8 ± 7.816.8 ± 1.320.5 ± 5.519.1 ± 4.850.25 ± 0.1030.77 ± 0.65
Treated group13.8 ± 3.9216.1 ± 3.3620.0 ± 4.0419.0 ± 3.610.14 ± 0.0150.64 ± 0.096c
Cool stress group16.5 ± 2.6715.7 ± 1.115.2 ± 2.0116 ± 2.170.27 ± 0.110.33 ± 0.12
DISCUSSION

Spleen is one of the five solid organs, which in Traditional Chinese Medicine (TCM), does not completely match the organ designated in western medicine from the standpoint of structure, location and function. It has the functions of digesting food, absorbing and transporting nutrients to the body tissues. The spleen also serves to control the blood and to keep the blood circulating within the vessels, and takes part in the regulation of fluid metabolism[32-38]. Spleen-Stomach theory forms the basis of diagnostic approach and treatment of Spleen-Stomach disease, Spleen deficiency syndrome is a multisystem and multiorgan functional impairment, but mainly manifest as digestive tract disturbance. Experimental researches on animal model and clinical studies on spleen deficiency syndrome have yielded fruitful results in this field which lead to a better understanding of its mechanism and help open a new avenue for treatment of diseases relevant to Spleen deficiency[21,39-47]. The Spleen stomach has various physiologic functions. such as: Spleen governs transport and transformation, Spleen-stomach transforms food into nutrients which are the sources of Qi and blood. Stomach governs down-bearing function and spleen governs up-bearing which signify the motility, secretory, assimilative, absorptive and dispersing functions of upper digestive tract, among which, gut hormones are involved[20,48-50]. Dysfunction of up-and down-bearing function of spleen-stomach can cause gastrointestinal disturbances and various spleen deficiency syndromes[1,2,19,20,51,52].

SP and VIP are both important gut Peptides, SP and VIP partly distributed in the mucosa of gastric antrum, the mucosa of the jejunum, ileum. And the central nervous system SP has a wide range of biological actions. In the intestine, VIP markedly stimulates intestinal secretion of electrolytes and hence of water. Its other actions include relaxation of intestinal smooth muscle; sphincters; dilation of peripheral blood vessels; and inhibition of gastric acid secretion.

Our previous studies included: The use of electrode and highly sensitive sensor to record alteration of gut electric activity and motility. To explore the potential role of gut peptides in spleen deficiency (SD), we studied immunoreactive Substance P, VIP, Calcitonin Gene Related Peptide (CGRP) levels in gastric antrum, duodenum and jejunual tissues in experimental SD rats by radioimmunoassys (RIA). The study suggested that motion frequency of several regions in SD rats was lower than that of control and treatment groups, respectively (P < 0.05). The minimal amplitude of electric activity was also lower than that of control and treatment respectively (P < 0.05). Correlation between motion frequency and its total amplitude index was different from various regions, the time of MMC was obviously less than that of the control, and the amplitude of motility was significantly higher than that of the control. The SP, VIP levels in antrum of SD rats were obviously less than that of the control, whereas, the SP and VIP levels in duodenum of SD rats were obviously higher than that of control (P < 0.05), but in jejunum only SP levels increased obviously than that of the control (P < 0.05). The VIP level in duodenum of SD rats was significantly less than that of treatment group (P < 0.05), but VIP level of treatment group was higher than that of the control (P < 0.05). As to CGRP level in antrum and small intestine, there was no obvious difference among the 3 groups.

The present study reveals changes SP and VIP in ileum of SD rats and cool stress rat. All these data imply that changes of SP and VIP levels in the antrum and the small intestine of SD rats may be closely related with the dysmotility of gastrointestinal , malabsorption and diarrhea. The Chinese herb (si junzi Tang) is capable of improving the spleen deficiency significantly and gastrointestinal electro-mechanical activity.

Footnotes

Edited by Wu XN

References
1.  Gao R, Li L, Lu Z. Clinical observation on 300 cases of angina pectoris treated by the spleen-stomach regulating method. J Tradit Chin Med. 1998;18:87-90.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Wu XN. Current concept of Spleen-Stomach theory and Spleen deficiency syndrome in TCM. World J Gastroenterol. 1998;4:2-6.  [PubMed]  [DOI]  [Cited in This Article: ]
3.  Straus E. Gastrointestinal hormones. Mt Sinai J Med. 2000;67:54-57.  [PubMed]  [DOI]  [Cited in This Article: ]
4.  Bierkamp C, Kowalski-Chauvel A, Dehez S, Fourmy D, Pradayrol L, Seva C. Gastrin mediated cholecystokinin-2 receptor activation induces loss of cell adhesion and scattering in epithelial MDCK cells. Oncogene. 2002;21:7656-7670.  [PubMed]  [DOI]  [Cited in This Article: ]
5.  Patten GS, Head RJ, Abeywardena MY, McMurchie EJ. An apparatus to assay opioid activity in the infused lumen of the intact isolated guinea pig ileum. J Pharmacol Toxicol Methods. 2001;45:39-46.  [PubMed]  [DOI]  [Cited in This Article: ]
6.  De Man JG, Moreels TG, De Winter BY, Bogers JJ, Van Marck EA, Herman AG, Pelckmans PA. Disturbance of the prejunctional modulation of cholinergic neurotransmission during chronic granulomatous inflammation of the mouse ileum. Br J Pharmacol. 2001;133:695-707.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Wise RM, Bass P, Oaks JA. Myoelectric response of the small intestine to the orad presence of the tapeworm Hymenolepis diminuta. J Parasitol. 2001;87:1255-1259.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Stebbing M, Johnson P, Vremec M, Bornstein J. Role of alpha(2)-adrenoceptors in the sympathetic inhibition of motility reflexes of guinea-pig ileum. J Physiol. 2001;534:465-478.  [PubMed]  [DOI]  [Cited in This Article: ]
9.  Shafik A, El-Sibai O, Ahmed A. Study of the mechanism underlying the difference in motility between the large and small intestine: the "single" and "multiple" pacemaker theory. Front Biosci. 2001;6:B1-B5.  [PubMed]  [DOI]  [Cited in This Article: ]
10.  Söderholm JD, Perdue MH. Stress and gastrointestinal tract. II. Stress and intestinal barrier function. Am J Physiol Gastrointest Liver Physiol. 2001;280:G7-G13.  [PubMed]  [DOI]  [Cited in This Article: ]
11.  Bayer S, Raul F, Boehm N, Klein A, Angel F. [Modulatory effects of polyamines and GABA on rat ileal motility in vitro]. Gastroenterol Clin Biol. 1999;23:824-831.  [PubMed]  [DOI]  [Cited in This Article: ]
12.  Chang IY, Glasgow NJ, Takayama I, Horiguchi K, Sanders KM, Ward SM. Loss of interstitial cells of Cajal and development of electrical dysfunction in murine small bowel obstruction. J Physiol. 2001;536:555-568.  [PubMed]  [DOI]  [Cited in This Article: ]
13.  Shibata C, Murr MM, Balsiger B, Anding WJ, Sarr MG. Contractile activity of circular smooth muscle in rats one year after small bowel transplantation: differing adaptive response of the jejunum and ileum to denervation. J Gastrointest Surg. 1998;2:463-472.  [PubMed]  [DOI]  [Cited in This Article: ]
14.  Pfefferkorn MD, Fitzgerald JF, Croffie JM, Gupta SK, Caffrey HM. Direct measurement of pancreatic enzymes: a comparison of secretagogues. Dig Dis Sci. 2002;47:2211-2216.  [PubMed]  [DOI]  [Cited in This Article: ]
15.  Takeuchi T, Fujita A, Roumy M, Zajac JM, Hata F. Effect of 1DMe, a neuropeptide FF analog, on acetylcholine release from myenteric plexus of guinea pig ileum. Jpn J Pharmacol. 2001;86:417-422.  [PubMed]  [DOI]  [Cited in This Article: ]
16.  Marinovich M, Viviani B, Capra V, Corsini E, Anselmi L, D'Agostino G, Di Nucci A, Binaglia M, Tonini M, Galli CL. Facilitation of acetylcholine signaling by the dithiocarbamate fungicide propineb. Chem Res Toxicol. 2002;15:26-32.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Venkova K, Sutkowski-Markmann DM, Greenwood-Van Meerveld B. Peripheral activity of a new NK1 receptor antagonist TAK-637 in the gastrointestinal tract. J Pharmacol Exp Ther. 2002;300:1046-1052.  [PubMed]  [DOI]  [Cited in This Article: ]
18.  Yin G, Zhang W, Li G. [Therapeutic effect of weikangfu on gastric precancerous disorder with spleen deficiency syndrome and its effect of gastric mucosal zinc, copper, cyclic adenosine monophosphate, superoxide dismutase, lipid peroxide and 3H-TdR lymphocyte conversion test]. Zhongguo Zhongxiyi Jiehe Zazhi. 2000;20:176-179.  [PubMed]  [DOI]  [Cited in This Article: ]
19.  Ren P, Huang X, Zhang L. [Effect of sijunzi decoction on gastric emptying rate in rat model of spleen deficiency syndrome]. Zhongguo Zhongxiyi Jiehe Zazhi. 2000;20:596-598.  [PubMed]  [DOI]  [Cited in This Article: ]
20.  Yin G, Zhang W, Xu F. [Effect of Weikangfu granule on ultrastructure of gastric mucosa in patients of precancerosis with spleen deficiency syndrome]. Zhongguo Zhongxiyi Jiehe Zazhi. 2000;20:667-670.  [PubMed]  [DOI]  [Cited in This Article: ]
21.  Xu L. Twenty-seven cases of spleen-qi deficiency syndrome treated by heat-producing needling at zusanli. J Tradit Chin Med. 2000;20:40-41.  [PubMed]  [DOI]  [Cited in This Article: ]
22.  Höckerfelt U, Franzén L, Kjörell U, Forsgren S. Parallel increase in substance P and VIP in rat duodenum in response to irradiation. Peptides. 2000;21:271-281.  [PubMed]  [DOI]  [Cited in This Article: ]
23.  Fujimiya M, Inui A. Peptidergic regulation of gastrointestinal motility in rodents. Peptides. 2000;21:1565-1582.  [PubMed]  [DOI]  [Cited in This Article: ]
24.  Chang FY, Doong ML, Chen TS, Lee SD, Wang PS. Vasoactive intestinal polypeptide appears to be one of the mediators in misoprostol-enhanced small intestinal transit in rats. J Gastroenterol Hepatol. 2000;15:1120-1124.  [PubMed]  [DOI]  [Cited in This Article: ]
25.  Huang X, Ren P, Wen AD, Wang LL, Zhang L, Gao F. Pharmacokinetics of traditional Chinese syndrome and recipe: a hypothesis and its verification (I). World J Gastroenterol. 2000;6:384-391.  [PubMed]  [DOI]  [Cited in This Article: ]
26.  Pei WF, Xu GS, Sun Y, Zhu SL, Zhang DQ. Protective effect of electroacupuncture and moxibustion on gastric mucosal damage and its relation with nitric oxide in rats. World J Gastroenterol. 2000;6:424-427.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Zhang XC, Gao RF, Li BQ, Ma LS, Mei LX, Wu YZ, Liu FQ, Liao ZL. Clinical and experimental study of therapeutic effect of Weixibaonizhuan pills on gastric precancerous lesions. World J Gastroenterol. 1998;4:24-27.  [PubMed]  [DOI]  [Cited in This Article: ]
28.  Xu CT, Pan BR. Current status of gene therapy in gastroenterology. World J Gastroenterol. 1998;4:85-89.  [PubMed]  [DOI]  [Cited in This Article: ]
29.  Xu CT, Pan BR. Current medical therapy for ulcerative colitis. World J Gastroenterol. 1999;5:64-72.  [PubMed]  [DOI]  [Cited in This Article: ]
30.  Yuan HY, Li Y, Yang GL, Bei DJ, Wang K. Study on the causes of local recurrence of rectal cancer after curative resection: analysis of 213 cases. World J Gastroenterol. 1998;4:527-529.  [PubMed]  [DOI]  [Cited in This Article: ]
31.  Yamamoto H, Umeda M, Mizoguchi H, Kato S, Takeuchi K. Protective effect of Irsogladine on monochloramine induced gastric mucosal lesions in rats: a comparative study with rebamipide. World J Gastroenterol. 1999;5:477-482.  [PubMed]  [DOI]  [Cited in This Article: ]
32.  Yin G, Zhang W, He X. [Histocytopathological study on gastric mucosa of spleen deficiency syndrome]. Zhongguo Zhongxiyi Jiehe Zazhi. 1999;19:660-663.  [PubMed]  [DOI]  [Cited in This Article: ]
33.  Zhu L, Yang ZC, Li A, Cheng DC. Reduced gastric acid production in burn shock period and its significance in the prevention and treatment of acute gastric mucosal lesions. World J Gastroenterol. 2000;6:84-88.  [PubMed]  [DOI]  [Cited in This Article: ]
34.  Zheng TZ, Li W, Qu SY, Ma YM, Ding YH, Wei YL. Effects of Dangshen on isolated gastric muscle strips in rats. World J Gastroenterol. 1998;4:354-356.  [PubMed]  [DOI]  [Cited in This Article: ]
35.  Li W, Zheng TZ, Qu SY. Effect of cholecystokinin and secretin on contractile activity of isolated gastric muscle strips in guinea pigs. World J Gastroenterol. 2000;6:93-95.  [PubMed]  [DOI]  [Cited in This Article: ]
36.  Shen XZ, Koo MW, Cho CH. Sleep deprivation increase the expression of inducible heat shock protein 70 in rat gastric mucosa. World J Gastroenterol. 2001;7:496-499.  [PubMed]  [DOI]  [Cited in This Article: ]
37.  Peng X, Feng JB, Wang SL. Distribution of nitric oxide synthase in stomach wall in rats. World J Gastroenterol. 1999;5:92.  [PubMed]  [DOI]  [Cited in This Article: ]
38.  Peng X, Feng JB, Yan H, Zhao Y, Wang SL. Distribution of nitric oxide synthase in stomach myenteric plexus of rats. World J Gastroenterol. 2001;7:852-854.  [PubMed]  [DOI]  [Cited in This Article: ]
39.  Li L, Jin NG, Piao L, Hong MY, Jin ZY, Li Y, Xu WX. Hyposmotic membrane stretch potentiated muscarinic receptor agonist-induced depolarization of membrane potential in guinea-pig gastric myocytes. World J Gastroenterol. 2002;8:724-727.  [PubMed]  [DOI]  [Cited in This Article: ]
40.  Yang WY, Liang R, Che JX. [Clinical study on relation between spleen-qi deficiency syndrome and the pancreatic exocrine function]. Zhongguo Zhongxiyi Jiehe Zazhi. 1996;16:414-416.  [PubMed]  [DOI]  [Cited in This Article: ]
41.  Zhang M, Zhang Z, Xia T. [Effect of sijunzi decoction on serum soluble intercellular adhesive molecule-1, interleukin-15 and monocyte antibody-dependent cell-mediated cytotoxicity in patients of spleen-deficiency]. Zhongguo Zhongxiyi Jiehe Zazhi. 1999;19:270-272.  [PubMed]  [DOI]  [Cited in This Article: ]
42.  Xu MY, Lu HM, Wang SZ, Shi WY, Wang XC, Yang DX, Yang CX, Yang LZ. Effect of devazepide reversed antagonism of CCK-8 against morphine on electrical and mechanical activities of rat duodenum in vitro. World J Gastroenterol. 1998;4:524-526.  [PubMed]  [DOI]  [Cited in This Article: ]
43.  Lin Z, Chen JD, Schirmer BD, McCallum RW. Postprandial response of gastric slow waves: correlation of serosal recordings with the electrogastrogram. Dig Dis Sci. 2000;45:645-651.  [PubMed]  [DOI]  [Cited in This Article: ]
44.  Xu D, Shen Z, Wang W. [Immunoregulation of Youguiyin, Sijunzitang, Taohong Siwutang in treating patients with deficiency of kidney, spleen and blood stasis syndrome]. Zhongguo Zhongxiyi Jiehe Zazhi. 1999;19:712-714.  [PubMed]  [DOI]  [Cited in This Article: ]
45.  Wang ZS, Cheung JY, Gao SK, Chen JD. Spatio-temporal nonlinear modeling of gastric myoelectrical activity. Methods Inf Med. 2000;39:186-190.  [PubMed]  [DOI]  [Cited in This Article: ]
46.  Tabor S, Thor PJ, Pitala A, Laskiewicz J. [Value of electrogastrographic parameters in evaluation of gastric myoelectrical activity]. Folia Med Cracov. 1999;40:27-42.  [PubMed]  [DOI]  [Cited in This Article: ]
47.  Abo M, Kono T, Wang Z, Chen JD. Impairment of gastric and jejunal myoelectrical activity during rectal distension in dogs. Dig Dis Sci. 2000;45:1731-1736.  [PubMed]  [DOI]  [Cited in This Article: ]
48.  Lin X, Hayes J, Peters LJ, Chen JD. Entrainment of intestinal slow waves with electrical stimulation using intraluminal electrodes. Ann Biomed Eng. 2000;28:582-587.  [PubMed]  [DOI]  [Cited in This Article: ]
49.  Lin X, Peters LJ, Hayes J, Chen JD. Entrainment of segmental small intestinal slow waves with electrical stimulation in dogs. Dig Dis Sci. 2000;45:652-656.  [PubMed]  [DOI]  [Cited in This Article: ]
50.  Abo M, Liang J, Qian L, Chen JD. Distension-induced myoelectrical dysrhythmia and effect of intestinal pacing in dogs. Dig Dis Sci. 2000;45:129-135.  [PubMed]  [DOI]  [Cited in This Article: ]
51.  Zeng J, Dai X, Yang J. [159 sterility patients of yang-deficiency of spleen and kidney treated by shouwu huanjing capsule]. Zhongguo Zhongxiyi Jiehe Zazhi. 1998;18:477-479.  [PubMed]  [DOI]  [Cited in This Article: ]
52.  Muth ER, Koch KL, Stern RM. Significance of autonomic nervous system activity in functional dyspepsia. Dig Dis Sci. 2000;45:854-863.  [PubMed]  [DOI]  [Cited in This Article: ]