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World J Clin Cases. Jan 21, 2022; 10(3): 753-761
Published online Jan 21, 2022. doi: 10.12998/wjcc.v10.i3.753
Lung injury after cardiopulmonary bypass: Alternative treatment prospects
Xue-Mei Zheng, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610000, Sichuan Province, China
Zhuo Yang, Department of Pharmacy, Chengdu Women’s and Children’s Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610000, Sichuan Province, China
Guang-Li Yang, Department of Medical Administration, Chengdu Women’s and Children’s Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610000, Sichuan Province, China
Yan Huang, National Institute of Drug Clinical Trial, Chengdu Women’s and Children’s Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610000, Sichuan Province, China
Jie-Ru Peng, Department of Medical Records Statistics, Chengdu Women’s and Children’s Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610000, Sichuan Province, China
Meng-Jun Wu, Department of Anesthesiology, The Affiliated Hospital, School of Medicine, Chengdu Women's and Children's Central Hospital, University of Electronic Science and Technology, Chengdu 610000, Sichuan Province, China
ORCID number: Xue-Mei Zheng (0000-0002-5380-5457); Zhuo Yang (0000-0001-5035-8156); Guang-Li Yang (0000-0002-1817-4303); Yan Huang (0000-0002-6372-9064); Jie-Rui Peng (0000-0002-2789-3019); Meng-Jun Wu (0000-0002-6899-4318).
Author contributions: Zheng XM, Yang Z and Yang GL contributed equally to this work; Wu MJ designed the research study; Zheng XM, Yang Z collected data from the literature; Zheng XM, Yang Z, Peng JR, Huang Y and Yang GL wrote the manuscript; Wu MJ conducted a review of the manuscript; all authors have read and approve the final manuscript.
Conflict-of-interest statement: The authors have no potential conflicts of interest to disclose.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Meng-Jun Wu, MD, PhD, Associate Chief Physician, Department of Anesthesiology, The Affiliated Hospital, School of Medicine, Chengdu Women's and Children's Central Hospital, University of Electronic Science and Technology, No. 1617 Riyue Avenue, Qingyang District, Chengdu 610000, Sichuan Province, China. 3400164739@qq.com
Received: August 10, 2021
Peer-review started: August 10, 2021
First decision: October 20, 2021
Revised: October 29, 2021
Accepted: December 23, 2021
Article in press: December 23, 2021
Published online: January 21, 2022

Abstract

Although the lung injury caused by cardiopulmonary bypass (CPB) has been extensively investigated, the incidence and mortality of lung injury after CPB remain a prominent clinical problem. The poor outcome has been attributed to multifactorial etiology, including the systemic inflammatory response and ischemia reperfusion (I/R) injury during CPB. Lung injury after CPB is a complex pathophysiological process and has many clinical manifestations of mild to severe disease. Which is associated with prognosis. To alleviate this lung injury, interventions that address the pathogenesis are particularly important. This review summarizes the pathogenesis, mechanism and treatment options of lung injury after CPB, such as lung protection with intralipid.

Key Words: Cardiopulmonary bypass, Lung injury, Pathogenesis, Treatment, Intralipid, Systemic inflammatory response syndrome

Core Tip: Respiratory dysfunction is a well-recognized side effect of cardiac surgery combined with cardiopulmonary bypass (CPB). The mechanism of lung injury after CPB is unclear, and the lack of effective treatment results in poor prognosis. This review summarizes the mechanisms of lung injury and proposes a new treatment option.
INTRODUCTION

More than 2 million patients worldwide undergo cardiac surgery annually, and most procedures use cardiopulmonary bypass (CPB)[1]. With the advent of extracorporeal circulation and improvement in surgical techniques, the incidence of postoperative complications after cardiac surgery should have been minimal. However, the incidence of pulmonary complications is 20%–35%, which is significant compared with complications after other types of surgery, partly due to systemic inflammatory response syndrome (SIRS) and ischemia reperfusion (I/R) injury during CPB[2-4]. Postoperative pulmonary complications after cardiac surgery with CPB, such as hypoxemia and acute respiratory distress syndrome, are thought to be significant, with poor prognosis and mortality up to 37.5%[4,5]. Survivors may have persistent physical, neuropsychiatric and neurocognitive disorders, which seriously affects quality of life and increases the medical burden.

In an attempt to minimize the deleterious effects of CPB, investigators have explored various strategies including improved CPB devices and methods[6-9] and pharmacological agents to reduce the systemic response. None of these interventions is, however, known to improve clinical outcomes. Steroids have been used for nearly 30 years as a basic treatment strategy for postoperative lung protection after CPB. However, there is conflicting evidence that steroids improve postoperative complications or reduce postoperative mortality in CPB patients[10-13].

Intralipid is a safe emulsion for intravenous application and is widely used in clinical settings[14]. Byrne et al[15] demonstrated that pretreatment with intralipid attenuated intestinal I/R injury in rats. It is not known whether intralipid has a protective effect in the prevention and treatment of lung injury after CPB. Review discusses the pathogenesis and treatment of lung injury caused by CPB, and explores the effects of intralipid on mitochondrial function of pulmonary vascular endothelial cells from three aspects: Mitochondrial respiratory chain, mitochondrial permeability transition pore (mPTP), and mitochondrial membrane potential (ΔΨm). This provides an additional view of the pulmonary protective mechanism of intralipid.

LITERATURE SEARCH

We conducted a narrative review of the mechanism and treatment of lung injury after CPB. PubMed was searched for articles published from December 1983 to July 2021. We carried out the search with the following MeSH or free-text terms: CPB, lung injury, fat emulsion, intralipid, lipid emulsion, coronary heart disease, ischemia reperfusion, on-pump coronary artery bypass graft (CABG), SIRS, reactive oxygen species (ROS), mPTP, and mitochondrial membrane potential. The search was limited to papers written in English, with no restrictions on the type of article. Two independent reviewers (XM and YZ) evaluated the articles for potential inclusion by screening titles and abstracts. The senior author (MJ) further evaluated the full text of articles with any disagreement.

MECHANISM OF LUNG INJURY AFTER CPB
SIRS

Our understanding of the SIRS to CPB began with the study of Kirklin et al[16] in the 1980s. SIRS is characterized by activation of platelets, neutrophils and macrophages, and cascades (coagulation, fibrinolytic, and kallikrein), which result in increased endothelial permeability and vascular and parenchymal damage[17,18]. These inflammatory responses are associated with the development of lung injury after CPB (Figure 1).

Figure 1
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Figure 1 A schematic representation of the mechanism of lung injury due to systemic inflammatory response syndrome. CPB: Cardiopulmonary bypass.

The contact of blood elements with the artificial surfaces of the CPB machine primes, heparin administration, and damage to the hematologic system from incisional, anesthesia and surgery can activate the complement system. C3a expression is activated mainly by CPB via the alternative pathway, and C4a expression is activated by the heparin protamine complex via the classical pathway. Complement (especially C3, C4a and C5a) promotes the release of mast cells and basophils in response to inflammatory mediators such as histamine, resulting in increased permeability of pulmonary epithelial cells and vasodilation[19].

There is increased expression of CD18 and CD11b adhesion molecules on the surface of neutrophils after chemotaxis of interleukin (IL)-8 and induction of C5a[20]. Activated neutrophils release proteolytic enzymes and oxygen-free radicals (O2- and HO), which directly or indirectly damage pulmonary vascular endothelial cells and promote their apoptosis, leading to increased intrapulmonary shunt fraction and pulmonary vascular resistance, and increased lung permeability with interstitial edema[21].

C3a is a powerful platelet aggregation agent. Heparin, hypothermia and duct disruption in CPB release platelets, and platelet activation leads to platelet aggregation, adhesion, consumption and thrombi formation by adsorption with fibrin[22]. Moreover, in late CPB, neutrophils adhere and transmigrate into the lung parenchyma and platelets are retained to block the pulmonary microcirculation. Activated platelets release 5-hydroxytryptamine, prostaglandin, thromboxane A2 and platelet factor 4, which damage pulmonary vascular endothelial cells and mediate lung parenchymal damage locally through cellular and tissue injury. Xiao et al[23] found that peripheral circulating platelets in CPB lung injury were significantly decreased. In addition, Kunitomo et al[24] reported that isolating 20% of platelets from blood before CPB and returning them after surgery significantly improved postoperative cardiopulmonary function, which may be related to the reduced effect of CPB on platelet number and function.

Complement activation, ischemia reperfusion and cytokine interactions can lead to release of cytokines, with tumor necrosis factor (TNF)-α[25] and IL-1, IL-6, IL-8 and IL-10 being the main ones clearly associated with lung injury[26]. TNF-α and IL-1 synergistically activate nuclear factor-κB to promote generation of cytokines and polymorphonuclear cells (PMNs), exacerbating the cascade of cell death signals. These, in turn, lead to endothelial cell swelling, plasma and protein extravasation into the interstitial tissue, aggregation of PMNs and macrophages at the injury site, and, finally, impedance of intra-alveolar cellular perfusion and oxygen exchange, causing lung injury.

Factor XII is activated by blood contact with CPB ducts and by vascular endothelial cell injury resulting in subendothelial collagen exposure, then factor XIIa activates the endogenous coagulation system and kallikrein, bradykinin production, vasodilation and increased permeability. Meanwhile, enhanced fibrinolysis and fibrin degradation products during CPB can lead to lung injury.

Lung I/R injury

The lungs have a dual blood supply from the bronchial artery and pulmonary artery. It has been shown that, under normal physiological conditions, the bronchial artery blood flow is 3%–5% of the total blood flow to the lungs[27]. The vena cava is cut off during CPB, and the metabolic demands of the lungs are totally dependent on oxygen supply from the bronchial arteries. Therefore, the lungs are excluded from the systemic circulation ischemia and hypoxia. Subsequently, ATP and lung surfactant are affected after CPB. Finally, lung permeability increases along with protein exudation. At this time, the lungs are in a hypoxic and relatively hypermetabolic state and are susceptible to endothelial cell injury. Vascular endothelial cells produce a large number of cytotoxic enzymes such as myeloperoxidase (MPO), leading to I/R injury. It has been shown that I/R injury leading to Na+ pump inactivation and Ca2+ overload is an important factor triggering lung tissue injury[28,29]. In addition, mitochondria are important targets of intracellular Ca2+ overload attack, and intracellular Ca2+-dependent proteases are activated, causing impaired energy metabolism and release of cytochrome C (CytC) and apoptosis-inducing factor from the inner and outer mitochondrial membrane gap. Meanwhile, reduced synthesis of endothelium-derived relaxing factor (NO) due to I/R injury can also mediate lung parenchymal injury[30].

ROS

Systemic inflammation, surgical trauma, and reperfusion after ischemia play a pivotal role in oxidative stress by initiating a series of biochemical events that result in the generation of excessive amount of ROS[31,32]. Lipid peroxidation is closely related to apoptosis[33]. During CPB, ischemic injury occurs when the blood supply to tissue is suboptimal and accompanied by cellular ATP depletion due to its degradation by hypoxanthine. During periods of stress, cell membrane surface NADH/NADPH oxidase is activated. Meanwhile, ROS levels can increase drastically, leading to substantial damage to many cellular molecules such as lipids, proteins and DNA[34]. Furthermore, ROS results in the production of CytC and damaged mitochondrial membranes with disruption of the alveolar barrier and apoptosis of alveolar epithelial cells[35].

ALTERNATIVE TREATMENT PROSPECT: INTRALIPID

Intralipid, is a safe lipid emulsion for intravenous application, which has been widely utilized as a vehicle for different drugs like propofol and etomidate[14]. It is also used for parenteral nutrition to supplement the body with energy and essential fatty acids. In addition, intralipid has been used in the treatment of cardiotoxicity caused by overdose of local anesthetics such as bupivacaine[36]. Recent animal studies have shown that postischemic administration of lipid emulsion protects the heart against I/R injury[14,37,38]. Meanwhile, clinical studies have also demonstrated that intralipid postconditioning reduces the release of markers of myocardial injury after heart valve replacement and has a cardioprotective effect[39]. In addition, animal studies also suggest that intralipid mitigates impaired pulmonary function induced by I/R through attenuation of local cellular injury and the subsequent SIRS[40]. Therefore, we hypothesize that there is a pulmonary protective function of intralipid, and it is necessary to explore its potential mechanism of action.

The lungs are especially susceptible to the inflammatory attack and I/R injury ascribed to the use of CPB[4]. Oxidative stress and massive release of ROS caused by I/R-induced lung injury, which can lead to functional changes and apoptosis of pulmonary microvascular endothelial cells, result in increased capillary permeability, impaired pulmonary diffusion function, and accumulation of fluid in the interstitial space[41,42]. In solid organs, electron conduction defects occur in ischemic/hypoxic cells, leading to irreparable mitochondrial damage, which is a key mechanism of I/R-induced lung injury[43]. Therefore, maintaining mitochondrial functional homeostasis makes it possible to mitigate I/R damage. Mitochondria store the energy generated as electrochemical potential energy in the inner membrane, resulting in an asymmetric distribution of H+ and other ion concentrations on both sides of the inner membrane to form the ΔΨm[44], which is reflective of metabolic function[45]. ΔΨm is essential for maintaining mitochondria for oxidative phosphorylation and production of ATP, and stability of ΔΨm depends on normal respiratory chain complex activity, proton flow and ATP synthesis[46]. Alteration in the activity of mitochondrial respiratory enzyme complexes during reperfusion of various tissues, which results in an excess of free radicals derived from oxygen and cellular ATP imbalance, has been reported in organs such as the heart, liver and brain[47,48]. Moreover, Sommer et al[49] found that the lungs suffer from the same mitochondrial damage as other solid organs in the pathological situation of I/R, and that changes in the degree of ΔΨm polarization are critical for the development of lung mitochondrial dysfunction[49]. In the postischemic reperfusion phase in the lungs, respiratory chain complex dysfunction, lipid membrane oxidation, and ATP reduction impair the stability of ΔΨm. The above studies suggest that maintaining the stability of ΔΨm is important to reduce lung I/R injury during the early postischemic reperfusion phase.

There is abundant evidence that intralipid can exert myocardial protective effects by inhibiting the opening of mPTP[14]. I/R injury leads to mitochondrial respiratory chain damage and impaired oxidative phosphorylation[50,51]. Mitochondrial damage generates reactive oxygen clusters through complexes I and III and ROS promote oxidative stress. Meanwhile, ROS act as signaling molecules for apoptosis by decreasing mitochondrial ΔΨm and increasing mPTP opening. In the early phase of reperfusion, Ca2+ overload and oxidative stress due to ischemia cause the opening of mPTP[52]. mPTP opening is a key event in cell death after I/R because it causes an abrupt increase in the permeability of the inner mitochondrial membrane to solutes with molecular weights up to 1500 Da, which further causes a decrease in mitochondrial membrane polarization, leading to a decrease in CytC release and matrix swelling, activating caspase 3- and 9-dependent apoptotic cascade responses[52,53]. As mentioned earlier, numerous studies have suggested that intralipid can inhibit the opening of mPTP in cardiomyocytes, therefore, the three aspects of mitochondrial respiratory chain, mPTP and ΔΨm make it possible for intralipid to improve mitochondrial function in pulmonary vascular endothelial cells for lung protection.

CONCLUSION

Despite the advances in extracorporeal circulation and surgical techniques of recent years, a significant proportion of patients still have a poor outcome. Ischemic and pharmacological preconditioning and postconditioning has been reported to ease I/R injury[38,54]. However, the lack conditions in the clinical setting are not as precisely defined as in the laboratory; therefore, ischemic modulation has limited clinical application[55]. Besides, it is reported that remote ischemic preconditioning does not reduce morbidity or mortality in patients undergoing cardiac surgery with CPB[56]. Therefore, from the view of clinical practice, pharmacological preconditioning or postconditioning is especially promising. Intralipid is a necessary fatty acid carrier and may be a promising approach to improve outcomes after CPB.

Intralipid can be used to treat the cardiotoxicity caused by local overdose of anesthetics and has been clinically proven[57]. The most supported dosing regimen is an intravenous bolus of 1–1.5 mL/kg 20% intralipid. Approximately 12 mL/kg intralipid is the upper limit for initial dosing in adults and 15 mL/kg in children[57-59]. Previous research has provided evidence that intralipid reduces myocardial infarct size and improves cardiac function by pre-reperfusion infusion[38,60,61]. Yuan et al[62] recently conducted a randomized controlled trial using intralipid to assess prognosis and cardiac function in adult cardiac surgery patients after extracorporeal circulation. A single intravenous bolus of intralipid (2 mL/kg, 20%) did not cause abnormal lipid metabolism, with no perioperative hepatic or renal dysfunction, or other related complications[39,62,63]. The duration of intravenous infusion of intralipid should be > 10 min as rapid administration of large amounts increases the risk of fat embolism. The dose of intralipid is selected on the basis of the pill dose when it is used in rescuing the cardiac arrest caused by local anesthetic toxicity, so it leads to a difference in the drug dose. Notably, some studies have found that short infusions of intralipid can cause elevated free fatty acids, induce insulin resistance and increase risk of hyperglycemic events[64], while hyperglycemia is an independent risk factor for mortality and postoperative complications in coronary heart disease surgery[65]. These may limit the use of intralipid on-pump CABG. However, Javaherforoosh Zadeh et al[66] showed that using adjusted tight glycemic control to a level that is near to normal during cardiac surgery may reduce hyperglycemic complications. Due to the lack of research on proper intravenous dosage of intralipid in lung injury after CPB, more data are needed to confirm the specific dose to be used.

The prevention and treatment of lung injury after CPB face many challenges. First, with the advent of extracorporeal circulation and improvement in surgical techniques, the incidence of postoperative complications of cardiac surgery should be minimal. However, the incidence of pulmonary complications and mortality rates are high. Second, the mechanism of lung injury caused by CPB is not clear and needs to be studied in depth. Third, there is a lack of effective treatment methods. The development and use of therapeutic agents against the lung injury after CPB are important. If intralipid demonstrates benefit, it would have rapid uptake globally and have tremendous impact.

Footnotes

Provenance and peer review: Unsolicited article; Externally peer reviewed.

Peer-review model: Single blind

Specialty type: Medicine, research and experimental

Country/Territory of origin: China

Peer-review report’s scientific quality classification

Grade A (Excellent): 0

Grade B (Very good): B

Grade C (Good): 0

Grade D (Fair): D

Grade E (Poor): 0

P-Reviewer: Glumac S, Karim HMR S-Editor: Fan JR L-Editor: A P-Editor: Fan JR

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