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The effects of ischaemic conditioning on lung ischaemia–reperfusion injury

Respiratory Research volume 23, Article number: 351 (2022) Cite this article

Abstract

Ischaemia–reperfusion injury (IRI) encompasses the deleterious effects on cellular function and survival that result from the restoration of organ perfusion. Despite their unique tolerance to ischaemia and hypoxia, afforded by their dual (pulmonary and bronchial) circulation as well as direct oxygen diffusion from the airways, lungs are particularly susceptible to IRI (LIRI). LIRI may be observed in a variety of clinical settings, including lung transplantation, lung resections, cardiopulmonary bypass during cardiac surgery, aortic cross-clamping for abdominal aortic aneurysm repair, as well as tourniquet application for orthopaedic operations. It is a diagnosis of exclusion, manifesting clinically as acute lung injury (ALI) or acute respiratory distress syndrome (ARDS). Ischaemic conditioning (IC) signifies the original paradigm of treating IRI. It entails the application of short, non-lethal ischemia and reperfusion manoeuvres to an organ, tissue, or arterial territory, which activates mechanisms that reduce IRI. Interestingly, there is accumulating experimental and preliminary clinical evidence that IC may ameliorate LIRI in various pathophysiological contexts. Considering the detrimental effects of LIRI, ranging from ALI following lung resections to primary graft dysfunction (PGD) after lung transplantation, the association of these entities with adverse outcomes, as well as the paucity of protective or therapeutic interventions, IC holds promise as a safe and effective strategy to protect the lung. This article aims to provide a narrative review of the existing experimental and clinical evidence regarding the effects of IC on LIRI and prompt further investigation to refine its clinical application.

Background

Ischaemia–reperfusion injury (IRI) encompasses the deleterious effects on cellular function and survival that result from the restoration of organ perfusion [1]. Counterintuitively, IRI further aggravates ischaemic organ damage as the degree of injury after reperfusion surpasses that caused by ischaemia per se [2]. It is mediated by sterile inflammation, enhanced oxidative stress and coagulation, endothelial dysfunction, and activation of cellular death pathways [1, 2]. Crucially, it is a systemic process with the potential to evoke distant organ injury and progress to multiple organ dysfunction syndrome [2]. Despite their unique tolerance to ischaemia and hypoxia, afforded by their dual (pulmonary and bronchial) circulation as well as direct oxygen diffusion from the airways [3], lungs are particularly susceptible to IRI (LIRI) [4]. Importantly, the cessation of ventilation leads to functional impairments similar to those induced by hypoperfusion [3], to which it is also interrelated by way of hypoxic pulmonary vasoconstriction (HPV) [5]. LIRI may be observed in a variety of clinical settings, including lung transplantation [4, 6], lung resections [7, 8], cardiopulmonary bypass (CPB) during cardiac surgery [9,10,11,12], aortic cross-clamping for abdominal aortic aneurysm (AAA) repair [13], as well as tourniquet application for orthopaedic operations [14]. It culminates in the breakdown of lung endothelial and epithelial barriers, leading to pulmonary oedema with attendant gas exchange impairment [4] and increased pulmonary vascular resistance resulting in pulmonary hypertension [15].

Ischaemic conditioning (IC) signifies the original paradigm of treating IRI. It entails the application of short, non-lethal ischemia and reperfusion manoeuvres to an organ, tissue, or arterial territory, which activates mechanisms that reduce IRI [16]. The concept of IC has several temporal and anatomical variations. In specific, the protective ischaemic stimulus may be applied before, during, or following the index reperfusion episode (pre-, per-, and post-conditioning respectively) with similar beneficial effects [16]. Furthermore, this intervention has systemic protective properties which are exploited by remote ischemic conditioning (RIC): biochemical and neuronal mechanisms confer protection to organs distant to the conditioning stimulus [16]. There is accumulating experimental and clinical evidence that IC may ameliorate LIRI in various pathophysiological contexts. In specific, it reduces the underlying oxidative stress and sterile inflammation in animal [17] and human models [7]. This is translated into decreased histologic damage [18], reduced pulmonary oedema [19], and improved respiratory function [8, 19] and pulmonary vascular haemodynamics [10, 20]. Considering the detrimental effects of LIRI, ranging from acute lung injury (ALI) following lung resections [15] to primary graft dysfunction (PGD) after lung transplantation [4], the association of these entities with adverse outcomes [4, 21], as well as the paucity of protective or therapeutic clinical interventions [4], ischaemic conditioning holds promise as a safe and effective strategy to protect the lung. This article aims to provide a review of the existing experimental and clinical evidence regarding the effects of IC on LIRI.

The pathophysiology of lung ischaemia reperfusion injury

Enhanced oxidative stress appears to play a prominent role in the pathophysiology of LIRI [22]. Ischaemia, in the presence or not of apnoea as determined by ventilatory manoeuvres, creates a hypoxic environment with inhibited mechanotransduction in the arterioles and capillaries [23]. This triggers the production of reactive oxygen species (ROS) by endothelial cells, macrophages, and other immune cells [24]. The lung antioxidative mechanisms are overwhelmed upon reperfusion, resulting in an imbalance between ROS production and clearance [22]. Eventually, direct oxidative damage ensues with carbonylation of proteins and peroxynitration of proteins, lipids, and DNA [25]. Furthermore, ROS instigate a robust innate immune response by activating alveolar macrophages, which in turn release proinflammatory cytokines, including interleukin (IL)-8, -12, 18, and tumour necrosis factor (TNF)-a [26]. Additionally, neutrophils are recruited [26], and in concert with macrophages further enhance ROS generation; thus, a self-perpetuating cycle of oxidative stress enhancement is created [27, 28]. These activated leucocytes transmigrate into the extravascular space and cause increased microvascular permeability, thrombosis, oedema, and parenchymal cell death, by way of proteases, elastases, and ROS production [2]. Adherence of neutrophils to the endothelium further promotes the formation of gaps between the endothelial cells [6]. Moreover, these inflammatory cascades trigger platelet aggregation and coagulation, leading to formation of microthrombi and microvascular constriction [29]. The attendant activation of vasoactive agents, including thromboxane A2 and platelet activating factor, further promotes oedema formation [29, 30]. LIRI is also characterised by apoptotic phenomena, in part initiated by inflammatory cytokines (including IL-1β, -2, -8, and TNF-a) and enhanced by the release of proapoptotic factors due to mitochondrial rupture [31]. More specifically, the hypoxia-induced adenosine triphosphate (ATP) deficiency induces dysfunction of ATP-dependent ion pumps that results in mitochondrial calcium overload [29]. This leads to increased permeability of the mitochondrial transition pores and swelling, eventually leading to rupture [31]. Type II epithelial cells play a key role as both victim and as culprit of LIRI, as their reperfusion-induced dysfunction leads to impaired production and composition of pulmonary surfactant [32]. Crucially, the above described prooxidative and inflammatory signalling may exert systemic effects: on the one hand, distant IRI is known to cause pulmonary injury [33]; on the other hand, LIRI induces remote organ inflammatory and oxidative damage [34], while unilateral lung reperfusion may lead to similar deleterious processes in the contralateral, non-ischaemic lung [35] (Fig. 1).

Fig. 1
figure 1

The pathophysiology of lung ischaemia reperfusion injury. Lung ischaemia reperfusion injury is the result of a robust inflammatory response and oxidative stress enhancement, which are instigated by ischaemia and further promoted by reperfusion. The attendant leucocyte migration and platelet activation result in alveolar-epithelial barrier impairment and pulmonary vasoconstriction, manifesting as noncardiogenic pulmonary oedema, pulmonary hypertension and deterioration of ventilation mechanics

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The clinical impact of lung ischaemia reperfusion injury

The end result of LIRI is disruption of the alveolar-capillary barrier, causing non-cardiogenic pulmonary oedema and ventilation-perfusion (V/Q) [5]. Total and extravascular lung water is increased, causing gas exchange and lung mechanics impairment, with decreased arterial oxygen tension (PaO2) [36], increased airway pressures and increased alveolar-arterial oxygen gradient [(A-a) DO2] [37]. In addition, the attendant defective surfactant production and composition leads to reduced static (Cs) and dynamic lung compliance (Cd), while further increasing (A-a) DO2 [38]. Moreover, pulmonary vascular resistance (PVR) is increased up to three-fold following reperfusion, mainly due to pulmonary precapillary vasoconstriction [39]. Thus, LIRI is further compounded by pulmonary hypertension, which might also additionally hydrostatically promote the formation of pulmonary oedema [40].

In the absence of specific diagnostic criteria, LIRI is a diagnosis of exclusion, manifesting clinically as ALI or acute respiratory distress syndrome (ARDS) [41]. It has a detrimental impact in various clinical scenarios, particularly following lung transplantation: LIRI leads to PGD, which is the major cause of both short- and long-term morbidity and mortality in this setting [15, 42]. Importantly, the incidence of severe (grade 3) PGD within 72 h of transplantation is approximately 30% [42], while PGD is also associated with late graft rejection, which is the primary mortality aetiology beyond 1 year of the procedure [43, 44]. ALI/ARDS is frequent following lung resections, with a reported incidence of 0.88%, 2.96%, and 7.9% following sublobar, lobar/bilobar resection, and pneumonectomy respectively [21]. The associated mortality is considerable, ranging from 22% in sublobar resections to 50% following pneumonectomy [21]. LIRI is also a major source of morbidity and mortality after cardiac surgery, as it contributes to the development of ARDS, with an incidence of up to 20% and a mortality reaching 80% [45]. Interestingly, hepatosplanchnic IRI in aortic surgery has been found to cause lung injury, with increased pulmonary leak index (PLI) in up to 74% of the patients, especially in cases involving clamping of major aortic branches and in direct correlation with the aortic clamping time [46]. ALI also complicates 30–50% of major trauma cases, with an associated mortality of 10% depending on the severity of lung dysfunction [47].

The protective effects of ischemic conditioning on lung ischaemia reperfusion injury—effects on oxidative stress and inflammation

Experimental evidence

One of the critical mechanisms mediating the protective effects of IC against LIRI is the alleviation of oxidative stress and inflammation. Li et al. were among the first to demonstrate this, in a canine model of lung transplantation (in situ LIRI). Specifically, IC by donor pulmonary hilar occlusion/reperfusion before transplantation was associated with reduced infiltration of the transplanted lung interstitium by polymorphonuclear leukocytes (PMNs) and reduced blood levels of malondialdehyde (MDA) and thromboxane B2 (TXB2) following reperfusion; on the contrary, superoxide dismutase (SOD) levels were higher, denoting a preserved antioxidant reserve [48]. Similarly, in a rat model experiment, IC decreased thiobarbituric acid reactive substances (TBARS) after lung storage, reflecting the decreased MDA levels [49]. Focusing on the fluid shifts caused by enhanced oxidative stress and inflammation, Gasparri et al. showed that 15, but not 5, minutes of transient lung ischaemia before lung preservation mitigated lung oedema upon reperfusion [50]. Soncul et al. utilised isolated lungs mounted on a modified Langendorff perfusion apparatus, where IC was related with reduced tissue and perfusate MDA levels [51]. In a similar IC protocol, tissue MDA levels were reduced, glutathione levels increased, intra-alveolar oedema and capillary congestion were prevented, while type II alveolar and endothelial cells were preserved [52]. Li et al. applied IC before sustained lung ischemia–reperfusion to rabbits. Lung MDA levels were lower and SOD levels were higher in the preconditioned lungs, with an attendant reduction in lung oedema and alveolar damage [53]. Friedrich et al. applied IC on a canine model of LIRI, whereby the reperfusion insult was preceded by either a single 5-min occlusion with a 15-min reperfusion period or two successive 10-min ischemia–reperfusion stimuli, and was followed by bronchoalveolar lavage (BAL). Interestingly, the former protocol resulted in reduced BAL fluid protein and TNF-a content, while the latter had no effect, highlighting the importance of the IC stimulus duration [54]. Jun et al. elucidated the genetic background of IC: conditioning of the donor lung resulted in downregulation of a vast array of inflammatory and immune mediator genes, including IL-1, IL-2, IL-3, IL-6, IL-15, TNF-a, intercellular adhesion molecule-2 (ICAM-2), vascular cell adhesion molecule-1 (VCAM-1), and activated leukocyte adhesion molecules [55].

Remote ischemic conditioning (RIC) appears to have similar effects to local IC on in situ LIRI, as demonstrated by Song et al.: 6 cycles of 10-s aortic occlusion/reperfusion protected from LIRI induced by lung hilar clamping. In more detail, alveoli were preserved with less neutrophilic infiltration and oedema, the increase in lung wet-to-dry weight ratio was prevented, while plasma IL-6, TNF-a, and ROS levels were reduced [17]. Waldow et al. similarly concluded that RIC prevented the IL-1β increase and abrogated the lung macrophage infiltration induced by LIRI [20]. RIC by hepatic hilar clamping also ameliorated the increase in IL-6 and TNF-a, reduced myeloperoxidase (MPO) activity (reflecting the respective lung neutrophil accumulation) and the BAL fluid leucocyte levels, in parallel with inhibited alveolar damage and reduced wet-to-dry lung ratio; apoptotic cascades were attenuated, with decreased cleaved caspase-3 expression and fewer apoptotic nuclei [19]. An interesting study by Zhou et al. highlighted the protection conferred against CPB-induced LIRI: RIC alleviated intra-alveolar neutrophil infiltration and alveolar wall thickening, reduced BAL fluid protein levels and lung wet-to-dry weight ratio, in parallel with increased anti-inflammatory IL-4 and IL-10 [56].

Besides in situ LIRI, conditioning exerts protection in cases of remote organ reperfusion. In the setting of aortic occlusion and reperfusion, RIC was associated with reduced alveolar oedema, congestion, and neutrophil infiltration [18, 57]. Similar benefits have been derived from hepatosplanchnic conditioning, which abrogated the P-selectin upregulation caused by IRI, with an attendant reduction in alveolar and perivascular neutrophil infiltration, reduced MDA levels, and preserved vascular permeability [58]. Likewise, hepatic or mesenteric conditioning reduced inflammatory cell infiltration in animals undergoing hepatosplanchnic reperfusion [59]. In concordance with these findings, Meng et al. showed that mesenteric conditioning decreased plasma and lung tissue TNF-a and IL-6 levels, in contrast with an increase in IL-10 levels, SOD and glutathione peroxidase activity. Moreover, endothelial and alveolar epithelial architecture were preserved, as was the integrity of type II alveolar cell mitochondria, with concurrently diminished wet-to-dry lung weight ratio and pulmonary microvascular dysfunction [60]. However, dos Santos et al. did not reveal any histologic preservation by IC; interestingly, mesenteric IRI caused only minimal lung injury, thereby narrowing the margins for demonstrating a protective effect [61].

Harkin et al. investigated the effects of IC on limb reperfusion-induced LIRI, by way of external iliac artery occlusion/reperfusion. IC attenuated the increase in plasma IL-6 and phagocytic priming, without affecting the TNF-a levels; lung tissue MPO increase was also diminished, as was the elevation of weight-to-dry weight ratio [62]. A similar study focused on unilateral lower limb ischaemia, utilising a left lower limb tourniquet. RIC resulted in decreased plasma TBARS, as well as reduced PMN infiltration and MPO activity in the lung, while protecting from alveolar and interstitial oedema, and alveolar haemorrhage [63].

Haemorrhagic shock resuscitation is hampered by multiorgan failure (MOF), which is the commonest cause of death after severe trauma [64]. The role of systemic inflammation and oxidative stress is pivotal [65], while respiratory failure is recognised among the commonest and deadliest complications thereof [64]. Jan et al. studied the effects of lower limb tourniquet occlusion/reperfusion on a rat model of haemorrhagic shock. IC significantly reduced plasma IL-6 levels, in parallel with diminished lung IL-6, PGE2, MDA, and BAL fluid protein concentration. The levels of macrophage inflammatory protein-2 (MIP-2), MPO activity, PMN-to-alveoli and wet-to-dry weight ratios were also decreased, in association with mitigated alveolar wall oedema, haemorrhagic changes, vascular congestion, and PMN infiltration [66]. In a comparable study, RIC inhibited the rise in plasma TNF-a levels, as well as the lung TNF-a mRNA and protein expression following shock resuscitation. Lung MPO activity and protein leakage into BAL fluid were similarly reduced [67].

The suspension of ventilation, in concert with the resultant HPV, result in a hypoxic and hypoperfused lung environment that instigates LIRI [3, 5]. Preliminary evidence in this context have been contradictory. Bergmann et al. exploited RIC in a swine model of one lung ventilation (OLV). On the one hand, lung TNF-a and BAL fluid leucocyte levels were reduced; on the other hand, serum IL-1β and IL-8 were not affected, while microhaemorrhage and alveolar oedema of the ventilated lung were enhanced [68].

The marked heterogenicity of experimental IC protocols obviates reaching a safe conclusion with regards to their differential efficacy. Up to six cycles of ischaemia/reperfusion, with individual cycle ischaemic durations ranging from 10 s to 15 min have been successfully utilised. Thus, it may be inferred that a cumulative ischaemic stimulus of 1 and up to 30 min may confer biochemical protection from LIRI, although the most commonly applied protocols comprised three or four 5- or 10-min ischaemia–reperfusion cycles (Tables 1, 3; Fig. 2).

Table 1 Experimental studies of the ischaemic conditioning/remote ischaemic conditioning effects on lung ischaemia reperfusion injury
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Fig. 2
figure 2

The protective effects of ischaemic conditioning from lung ischaemia reperfusion injury. Ischaemic conditioning mitigates leukocyte migration, oxidative stress and systemic inflammatory cascades, while circulating inflammatory cytokine and pulmonary vasoconstrictor levels are also reduced. These mechanisms culminate in the amelioration of alveolar and endothelial injury, resulting in protection from non-cardiogenic pulmonary oedema, improved gas exchange, improved lung mechanics and superior pulmonary haemodynamics

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Clinical evidence

The majority of clinical data pertaining to the investigation of IC effects on LIRI has been obtained in the context of CPB-induced IRI. Forty patients undergoing valve replacement were randomised to an IC or control group. Analysis of pulmonary vein blood showed that IC by way of aortic occlusion/reperfusion mitigated the increase in MDA, PMN, and TBX2 levels, while increasing SOD. Similarly, calcitonin gene-related peptide (CGRP) levels in coronary sinus blood were enhanced, denoting the activation of the associated anti-oxidant pathway, in parallel with reduced pulmonary oedema, haemorrhage, and PMN infiltration [10]. RIC has similar properties, as exemplified by Jin et al. who utilised upper limb and thigh cuff inflation/deflation in a randomised control trial (RCT) of 241 patients undergoing valvular replacement: conditioning reduced the levels of serum soluble intercellular adhesion molecule-1 (sICAM-1), endothelin-1 (ET-1), and MDA, while increasing NO concentration [69]. In an RCT of 60 infants undergoing ventricular septal defect (VSD) repair, Zhou et al. applied upper limb cuff inflation/deflation in the intervention group. Postoperatively, serum IL-6, -8, -10, and TNF-a levels were reduced, while coronary sinus MDA was reduced and SOD increased in preconditioned infants [12]. Nonetheless, these findings are not unequivocal. Lower limb cuff inflation/deflation was applied to children undergoing surgical repair of congenital heart defects, but the realised lung protection could not be associated with systemic inflammation, as IL-6, -8, -10, and TNF-a levels were not affected by RIC [70]. Similarly, Hu et al. conducted an RCT that included 201 patients undergoing valve replacement, whereby RIC did not affect hypersensitive C-reactive protein (hsCRP) levels [11].

IC has been utilised in patients undergoing thoracic surgical operations. Chen et al. have been among the first to implement preconditioning in patients undergoing pneumonectomy: in a small study of 20 patients, a single pulmonary artery occlusion/reperfusion manoeuvre resulted in increased CGRP and SOD levels [71]. Li et al. randomised 216 patients undergoing elective lung resection to either a RIC, or a standard thoracic surgical treatment arm. Upper limb cuff inflation/deflation significantly reduced IL-6, TNF-a, and MDA levels post-operatively [7]. An analogous RCT was performed in 55 patients undergoing lobectomy for lung cancer, whose blood and exhaled breath condensate (EBC) were examined to determine the levels of oxidative stress. RIC mitigated oxidative stress, as denoted by reduced 8-isoprostane, cumulative nitrate and nitrite, hyperoxide, and acidity in the EBC samples of preconditioned patients; blood 8-isoprostane as well as cumulative nitrate and nitrite were also reduced in the RIC arm [8]. These findings were not reproduced in the pilot RCT by Lin et al. who randomised 60 patients undergoing bilateral sequential lung transplantation to a RIC or a standard treatment arm: IL-2, -6, -8, -10, TNF-a, interferon-gamma (IFN-γ), interferon gamma-induced protein 10, monocyte chemoattractant protein-1 (MCP-1), and chemokine ligand 5 (CCL5) did not differ between the two study groups [72].

Aortic cross-clamping during open abdominal aortic aneurysm repair (AAA) is known to trigger a systemic inflammatory response with an attendant accentuation of oxidative stress [33]; these cascades may progress to MOF, which underlies up to 25% of peri-operative deaths in this setting [73]. Against this background, the effects of RIC in the form of upper limb cuff inflation/deflation were evaluated in an RCT of 62 patients undergoing open AAA repair. RIC attenuated the post-operative increase in IL-6, TNF-a, and MDA levels, while increasing the activity of SOD [13]. Limb reperfusion may also induce MOF through comparable mechanisms [74]. Lin et al. studied 30 patients undergoing lower extremity surgery, necessitating sustained thigh tourniquet application. When this was preceded by IC, the rise in plasma IL-6, -8, and MDA after limb reperfusion was mitigated [14].

Similar to experimental investigations, clinical IC protocols have not been standardised. However, three 5-min ischaemia–reperfusion cycles have been most commonly utilised and may confer a biochemically determined protection from LIRI in a variety of clinical settings, although some studies have shown a neutral effect (Tables 2, 3; Fig. 2).

Table 2 Clinical studies of the ischaemic conditioning/remote ischaemic conditioning effects on lung ischaemia reperfusion injury
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Table 3 Summary of the protective effects of ischaemic conditioning from lung ischaemia–reperfusion injury
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The protective effects of ischemic conditioning on lung ischaemia reperfusion injury—effects on respiratory function and pulmonary haemodynamics

Experimental evidence

The oxidative stress and inflammatory response alleviation conferred by IC may be functionally translated into improved respiratory function and pulmonary haemodynamics. In the canine transplantation model studied by Li et al. donor lung IC was associated with increased mixed venous oxygen tension (PvO2) and reduced mean pulmonary artery pressure (mPAP) following reperfusion [48]. Du et al. also provided evidence of improved gas exchange, as denoted by higher arterial oxygen (PaO2) and decreased carbon dioxide tension (PaCO2) levels [49]. Similar oxygenation improvement has been demonstrated in the form of increased veno-arterial oxygen pressure gradients [50], while Soncul et al. concluded that IC ameliorated the increase in pulmonary artery pressure (PAP) caused by LIRI [51]. IC also preserved pulmonary arterial endothelial function in the study of Kandilci et al., reflected on decreased pulmonary perfusion pressures in response to histamine [52]. Further expanding the evidence above, Li et al. showed that PO2 is increased and mPAP decreased by IC [53]. Data of improved Cd have also been provided, in parallel with higher PaO2 and PvO2 levels; however, in the same study pulmonary vascular resistance (PVR) was not significantly affected [54]. Featherstone et al. reported analogous improvement in lung compliance; nonetheless, oxygenation and PVR did not differ between the preconditioned and the control groups [75].

RIC exerts comparable protective effects: gas exchange was significantly improved in the context of an in situ LIRI model, with increased PaO2 and decreased PaCO2, in the studies of Luo et al. [19] and Song et al. [17]. Waldow et al. showed that RIC improved PaO2 and PvO2, in parallel with a reduction in PAP and PVR [20]. In a setting of CPB-induced LIRI, evidence of superior total lung capacity (TLC) and Cd, as well as reduced airway resistance (Raw) was provided [56]. Comparably, Raw was lower upon exposure to CPB with a resultant decrease in ventilation pressures and a trend for lung compliance improvement in the study of Kharbanda et al. [76]. In an interesting study of coronary occlusion/reperfusion, simulating an off-pump coronary artery bypass stimulus, RIC increased PaO2 and P/F ratio, while decreasing PVR and PAP [77].

Investigating LIRI within the realms of remote reperfusion injury, Harkin et al. showed an improvement in PaO2 and (A-a) DO2 with an attendant reduction in mPAP following limb reperfusion in preconditioned animals [62]. Jan et al. demonstrated similar protective properties after resuscitation from haemorrhagic shock, with increased PaO2 and decreased (A-a) DO2, with an attendant amelioration of acidosis, as pH and base excess were increased by IC [66]. Interestingly, Bergmann et al. highlighted the improved respiratory function conferred by IC during OLV: oxygenation index [fraction of inspired oxygen (FIO2) * mean airway pressure (Paw mean)/PaO2)] was lower after RIC, with an attendant increase in venous oxygen saturation (SvO2) [68].

In summary, most experimental studies have reported improvements in gas exchange, respiratory mechanics, and pulmonary haemodynamics by IC. Interestingly, local conditioning appears to exert similar effects to RIC, both in settings of in situ as well as remote reperfusion injury. Thus, the systemic nature of the underlying processes has been consistently demonstrated (Tables 1, 3; Fig. 2).

Clinical evidence

There is accumulating clinical evidence delineating the effects of IC against LIRI in several pathophysiological contexts. Li et al. investigated the application if IC in patients exposed to CPB and revealed that preconditioning reduced PVRI and mPAP, while increasing PaO2; importantly, there was an attendant reduction in pulmonary complications (lobar collapse, pneumonitis, pneumothorax) and mechanical ventilation time [10]. In a similar cohort of patients, RIC conferred a decrease in (A-a) DO2, respiratory index [(A-a) DO2/PaO2], as well as the incidence of ALI [69]. Zhou et al. also concluded that RIC improved RI and decreased static (Cs) and dynamic lung compliance (Cd) [12], while the incidence of ALI was reduced in patients undergoing RIC during their valve replacement, despite the fact that (A-a) DO2 was not affected [11]. Moreover, RIC applied both before and after CBP in patients undergoing valvular replacement improved P/F ratio and reduced the incidence of mechanical ventilation beyond 48 h; Cs and Cd remained unchanged [78]. However, Cheung et al. did not reproduce any improvements in either oxygenation or compliance; nonetheless, Raw was reduced in preconditioned patients [70]. Hong et al. also showed a neutral effect of RIC on oxygenation and mechanical ventilation duration; however, the included patients underwent off-pump CABG, which obviates the exposure to CPB [79]. Additional studies have shown a lack of improvement in respiratory indices or outcomes, but no inflicted harm [80,81,82].

The results of the studies focusing on patients undergoing lung resections uniformly support the notion that IC confers significant protection from LIRI. RIC abrogated the deleterious effects of OLV on respiratory function, as denoted by improvements in P/F ratio, (A-a) DO2, and arterial-alveolar oxygen tension ratio (a/A ratio), with an attendant decreased ALI incidence; Cs and Cd were also significantly increased [7]. Concordant evidence was provided by García-de-la-Asunción et al., who showed an improvement in PaO2, (A-a) DO2, P/F and a/A ratio, and RI [8]. Chen et al. also demonstrated increased pulmonary venous oxygen tension in patients undergoing pneumonectomy [71]. In an important pilot RCT of RIC within the context of lung transplantation by Lin et al., preconditioning was associated with a trend for decreased PGD and biopsy-proven rejection risk, while P/F ratio was significantly increased in the subgroup of patients with restrictive lung disease [72]. RIC protects from the lung dysfunction triggered by splanchnic IRI, as shown by the RCT of Lin et al., whereby preconditioned patients undergoing AAA repair benefited from higher a/A ratio, lower (A-a) DO2 and RI, as well as improved Cs and Cd [13]. Comparable effects have been demonstrated following lower limb reperfusion: RIC resulted in improved PaO2, a/A ratio, (A-a) DO2, and RI [14].

Thus, despite the contradictory evidence provided by studies of cardiac surgery patients, the majority of data obtained in clinical settings that entail in situ lung, as well as hepatosplanchnic and limb reperfusion underlines the beneficial effects obtained from IC: respiratory function and ventilation mechanics may improve, while respiratory complications may be averted (Tables 2, 3; Fig. 2).

Conclusions

LIRI has a detrimental effect on respiratory function and pulmonary haemodynamics, with dismal consequences for patient prognosis in a variety of clinical settings. The abundance of experimental evidence revealing the beneficial effects of IC, both on the underlying inflammatory and oxidative cascades, as well as the resultant functional derangements is being gradually complemented by encouraging clinical data. Given its promising preliminary results, safety, and ease of application, IC appears to be an intervention worth of further investigation and a useful addition to our deficient armamentarium against LIRI.

Availability of data and materials

Not applicable.

Abbreviations

AAA:

Abdominal aortic aneurysm

ALI:

Acute lung injury

ARDS:

Acute respiratory distress syndrome

ATP:

Adenosine triphosphate

(A-a) DO2:

Alveolar-arterial oxygen gradient

BAL:

Bronchoalveolar lavage

CCL5:

Chemokine ligand 5

Cd:

Dynamic lung compliance

CGRP:

Calcitonin gene-related peptide

CPAP:

Continuous positive airway pressure

Cs:

Static lung compliance

EBC:

Exhaled breath condensate

ET-1:

Endothelin-1

FIO2:

Fraction of inspired oxygen

HPV:

Hypoxic pulmonary vasoconstriction

hsCRP:

Hypersensitive C-reactive protein

IC:

Ischaemic conditioning

IFN-γ:

Interferon-gamma

IL:

Interleukin

IRI:

Ischaemia–reperfusion injury

LIRI:

Lung ischaemia–reperfusion injury

MCP-1:

Monocyte chemoattractant protein-1

MDA:

Malondialdehyde

MIP-2:

Macrophage inflammatory protein-2

MOF:

Multiorgan failure

mPAP:

Mean pulmonary artery pressure

MPO:

Myeloperoxidase

OLV:

One lung ventilation

PaCO2:

Arterial carbon dioxide tension

PaO2:

Arterial oxygen tension

PAP:

Pulmonary artery pressure

Paw:

Airway pressure

PEEP:

Positive end-expiratory pressure

PGD:

Primary graft dysfunction

PMN:

Polymorphonuclear leucocyte

PvO2:

Mixed venous oxygen tension

PVR:

Pulmonary vascular resistance

PVRI:

Pulmonary vascular resistance index

P/F ratio:

Ratio of the partial pressure of oxygen to the inspired fraction of oxygen

Raw:

Airway resistance

RCT:

Randomised control trial

RIC:

Remote ischemic conditioning

ROS:

Reactive oxygen species

sICAM-1:

Serum soluble intercellular adhesion molecule-1

SOD:

Superoxide dismutase

SvO2:

Venous oxygen saturation

TBARS:

Thiobarbituric acid reactive substances

TLC:

Total lung capacity

TNF-a:

Tumour necrosis factor-alpha

TXB2:

Thromboxane B2

VCAM-1:

Vascular cell adhesion molecule-1

VSD:

Ventricular septal defect

V/Q mismatch:

Ventilation-perfusion mismatch

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  1. Dimitrios Vlastos

    Present address: , Liverpool, UK

Authors and Affiliations

  1. Department of Vascular Surgery, Countess of Chester Hospital, Chester, UK

    Dimitrios Vlastos

  2. Second Department of Cardiology, Attikon University Hospital, Athens, Greece

    Dimitrios Vlastos, Stefanos Vlachos & Ignatios Ikonomidis

  3. Department of Cardiac Surgery, Liverpool Heart and Chest Hospital, Liverpool, UK

    Mohamed Zeinah & Agni Salem

  4. Ain Shams University, Cairo, Egypt

    Mohamed Zeinah

  5. Department of Vascular Surgery, Royal Liverpool University Hospital, Liverpool, UK

    George Ninkovic-Hall

  6. Department of Cardiothoracic Surgery, NHS Golden Jubilee National Hospital, Glascow, UK

    Athanasios Asonitis

  7. Department of Thoracic Surgery, Royal Brompton and Harefield NHS Foundation Trust, London, UK

    Hemangi Chavan, Abdullah Al Shammari, José María Alvarez Gallesio & Aina Pons

  8. Department of Minimally Invasive Cardiac Surgery, Metropolitan General Hospital, Athens, Greece

    Lazaros Kalampalikis

  9. School of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece

    Ioanna Andreadou

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All authors discussed the literature and contributed to the final manuscript; DV: Conception or design of the work, data collection, data analysis and interpretation, drafting the article, critical revision of the article; MZ: Conception or design of the work, data collection, data analysis and interpretation, drafting the article, critical revision of the article,; GNH: Conception or design of the work, data collection, data analysis and interpretation, drafting the article, critical revision of the article; SV: data collection, data analysis and interpretation, drafting the article; AS: data collection, data analysis and interpretation, drafting the article; AA: data collection, data analysis and interpretation, drafting the article; HC: data collection, data analysis and interpretation, drafting the article; LK: data collection, data analysis and interpretation, drafting the article; AAS: data collection, data analysis and interpretation, drafting the article; JMAG: data collection, data analysis and interpretation, drafting the article; AP: data collection, data analysis and interpretation, drafting the article; IA: Conception or design of the work, data collection, data analysis and interpretation, drafting the article, critical revision of the article; II: Conception or design of the work, data collection, data analysis and interpretation, drafting the article, critical revision of the article. All authors read and approved the final manuscript.

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Vlastos, D., Zeinah, M., Ninkovic-Hall, G. et al. The effects of ischaemic conditioning on lung ischaemia–reperfusion injury. Respir Res 23, 351 (2022). https://doi.org/10.1186/s12931-022-02288-z

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Respiratory Research

ISSN: 1465-993X

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