Preconditioning somatothermal stimulation on Qimen (LR14) reduces hepatic ischemia/reperfusion injury in rats
© Hsieh et al.; licensee BioMed Central Ltd. 2014
Received: 21 June 2013
Accepted: 6 January 2014
Published: 13 January 2014
In human beings or animals, ischemia/reperfusion (I/R) injury of the liver may occur in many clinical conditions, such as circulating shock, liver transplantation and surgery and several other pathological conditions. I/R injury has a complex pathophysiology resulting from a number of contributing factors. Therefore, it is difficult to achieve effective treatment or protection by individually targeting the mediators. This study aimed at studying the effects of local somatothermal stimulation preconditioning on the right Qimen (LR14) on hepatic I/R injury in rats.
Eighteen male Sprague-Dawley rats were randomly divided into three groups. The rats were preconditioned with thermal tolerance study, which included one dose of local somatothermal stimulation (LSTS) on right Qimen (LR14) at an interval of 12 h, followed by hepatic ischemia for 60 min and then reperfusion for 60 min. Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) have been used to assess the liver functions, and liver tissues were taken for the measurements such as malondialdehyde (MDA), glutathione (GSH), catalase (CAT), superoxidase dismutase (SOD), and myeloperoxidase (MPO).
The results show that the plasma ALT and AST activities were higher in the I/R group than in the control group. In addition, the plasma ALT and AST activities decreased in the groups that received LSTS. The hepatic SOD levels reduced significantly by I/R injury. Moreover, the hepatic MPO activity significantly increased by I/R injury while it decreased in the groups given LSTS.
Our findings show that LSTS provides a protective effects on the liver from the I/R injury. Therefore, LSTS might offer an easy and inexpensive intervention for patients who have suffered from I/R of the liver especially in the process of hepatotomy and hepatic transplantation.
KeywordsIschemia-reperfusion Qimen (LR14) Superoxidase dismutase Myeloperoxidase
In human beings or animals, ischemia-reperfusion (I/R) injury of the liver may occur in many clinical conditions, such as circulating shock , disseminated intravascular coagulation , liver transplantation and surgery , cardiac failure and arrest, alcohol toxicity and several other pathological conditions. Different injury mechanisms contribute to the overall pathophysiology of the hepatic I/R injury. Because the liver is a highly oxygen-utilizing organ; therefore, the impairment of blood flow will rapidly cause hepatic hypoxia, which may progress to absolute anoxia especially in the pericentral regions of the liver lobe [4, 5]. Therefore, it is very important to investigate the proper treatments for the I/R injury of the liver.
Oxygen-derived free radicals play a crucial role in I/R injury in many organs such as the heart and the liver [6, 7]. Among the systemic consequences of reperfusion, lipid peroxidation is probably the most severe effect caused by free radicals, which results in structural and functional derangement and death of cells eventually [8, 9]. Several lines of evidences have shown that HSP70 is a general anti-apoptotic protein, which protects cells from cytotoxicity induced by oxidative stress or chemotherapeutic agents .
Among the numerous complementary and alternative medicine therapies, acupuncture and moxibustion are ancient Chinese therapies that are most widely accepted as in the treatment of many diseases. There have been various studies on the mechanisms and efficacy of acupuncture and moxibustion. In addition, many researchers using the protocols of evidence-based medicine have proved that acupuncture is effective in treating chronic low back pain and digestive disorders , and also found moxibustion preconditioning protects the ischemic and anoxic brain tissue by increasing the activity of endogenous antioxidase . Moreover, many hypotheses have been proposed to address the physiological mechanisms mediated by the action of acupuncture and moxibustion. In general, a large number of scientific studies have recently established strong evidence on the higher efficacy of acupuncture and moxibustion based on their clinical use over millenniums of years than that of the traditional treatment [13–15].
There are many modalities, including chemical and physical preconditioning, used to protect the organs from I/R injury. Massage, acupressure, chiropractic health care, exercise and hyperthermia et al. have been employed as treatment strategies for neuromuscular disorders or other diseases [16–19]. Recently, preconditioned local somatothermal stimulation (LSTS) has been proved to protect the heart and liver, increaseing the neuromuscular plasticity against I/R injury . Therefore, LSTS is a maneuver similar to local heat therapy or the moxibustion technique in traditional Chinese medicine. Moreover, previous studies have demonstrated that the preconditioned LSTS on the right seventh intercostal nerve territory could increase hepatic HSP70 synthesis and protect the liver from I/R injury in rats . Interestingly, the critical temperature evoking such visceral responses was around 41°C to 43°C, which was similar to those inducing HSP expression in a wide range of studies [21–24]. The induction of HSPs may afford protection from subsequent insults by decreasing leukocyte infiltration of postischemic tissues .
In our previous study, there are two possibilities to explain a somatovisceral reflex, namely, meridian theory and neuro-reflex theory. In meridian theory, Qimen (LR14) is an acupoint in the liver meridian. Accumulating evidence has demonstrated that there are convergent connections between somatic- and visceral neurons of the same or similar nerve territory during embryonic development. Besides, there is evidence that stimulation on an acupoint would regulate the corresponding organs through a complete loop of somatovisceral reflex, including receptors, afferent limbs, central system, efferent limbs and the target organ. Our previous work has demonstrated that the visceral response inhibited by blocking the afferent limb was blocked by local anesthesia . Nonetheless, the possibility of the involvement of meridian theory can not be completely ruled out. In this study, we proved that the application of LSTS to the right Qimen (LR14) could induce the hepatic gene expression of HSP70, and this paper mainly focuses on whether LSTS passes through different pathway to protect the liver against subsequent I/R injury?
Eighteen male Sprague-Dawley rats each weighing 250–300 g, had been obtained from the animal center of the National Science Council, Taiwan, Republic of China. They were fed with standard diets and water ad libitum and treated under the regulations of the “Guide for the Care and Use of Laboratory Animals” (National Academy Press; 2011). The studies of these rats were approved by the ethics committee for animal study of National Yang-Ming University, Taipei, Taiwan, Republic of China.
Local heat stress by local somatothermal stimulation
Application of local heat stress instead of using whole-body hyperthermia had been achieved by means of LSTS on skin areas with no direct contact with the skin surface. Conventional application of local heat therapy is supposed to evoke multiple sensory stimulation such as temperature, pressure, pain, and touch. In order to avoid causing any interference with the data interpretation by such multisensory stimulation, temperature was used as the sole stimulator in this study. The effect of LSTS done by using a heat generator (120 Watt. electric heating rod, Jise Co.) had been reported in our previous study regarding its relaxation effects on the sphincters of Oddi in cats, rabbits and the internal sphincters in rabbits [22, 24]. In brief, LSTS had been achieved by the application of a heat generator supplying a single heat source on and above the skin areas when the skin temperature fluctuated above and below the critical point of 41°C. This was done by intermittently turning the switch of the heat generator on and off, namely, 4 min on and 5 min off for three courses . In total, one dose of LSTS was completed in 27 min. A tinfoil paper with holes of 0.5 cm in diameter had also been used so that the heat generator could just focus on one point above the skin surface without insulation. Finally, we used a digital displayed thermometer to confirm that the critical heat point (41°C) was reached.
Preconditioning by LSTS
Animal model and parameters for the I/R injury of the liver
The model of rats with I/R injury was created as previously described [26, 27]. In brief, male Sprague-Dawley rats were anesthetized with urethrane (1.25 g/kg, IP), and the trachea was cannulated for artificial respiration with a ventilator. Polyethylene (PE-50) catheters were cannulated into the femoral artery to monitor the blood pressure with a polygraph (Gould, RS 2400). The liver was exposed through an upper midline incision, and two pieces of fine silk were looped along the right and left branches of the portal vein, hepatic artery, and bile duct. The procedure whereby the silk was inserted into a snare with a piece of polyethylene (PE-90) which allowed the occlusion of the blood supply to either the median and left lobes (left branch). For the I/R injury study, ischemia of the median/left lobes were maintained for 60 min followed by reperfusion of the median/left lobes with immediate occlusion of the right lobe vasculature for another 60 min. One hour after the completion of the reperfusion procedure, the initial ischemic-reperfused median/left lobes were resected and tested for myeloperoxidase (MPO), malondialdehyde (MDA), glutathione (GSH), catalase (CAT), superoxidase dismutase (SOD) measurement. Blood samples for ALT/AST measurement were collected immediately after the femoral catheterization and the completion of the reperfusion procedure.
Eighteen male Sprague-Dawley rats were randomly divided into three groups, which were the: control, I/R and I/R + LSTS groups, where each group had six rats (n = 6). In the control group, none of the rats were treated with LSTS, nor subjected to the I/R liver injury. In the I/R group, the rats were subjected to 60 min of hepatic ischemia followed by 60 min of reperfusion period. In the I/R + LSTS group, the rats were preconditioned for thermal tolerance study, which included one dose of LSTS on the right Qimen (LR14) at an interval of 12 h then hepatic ischemia for 60 min followed by reperfusion for 60 min.
Hepatic SOD assay
The hepatic SOD activity was determined by using a commercialized chemical SOD assay kit (Cayman Chemical Co.). The kit utilizes a tetrazolium salt for the detection of superoxide radicals generated by xanthine oxidase and hypoxanthine. The collected 1 gm of liver tissues were homogenized in 5 ml of cold buffer (20 mM HEPES buffer, pH 7.2, containing 1 mM EDTA, 210 mM mannitol, and 70 mM sucrose) and centrifuged at 1,500 × g for 5 min at 4°C. The reaction was initiated by adding xanthine oxidase and incubating at room temperature for 20 min, and then, the absorbance of each sample was read at 450 nm.
Hepatic CAT assay
The CAT activity was determined by using a commercialized chemical CAT assay kit (Cayman Chemical Co.). The kit utilizes the peroxidatic function of CAT for the measurement of enzyme activity. The collected 1 gm of liver tissues were homogenized in 5 ml of cold buffer (50 mM potassium phosphate, pH 7.0, containing 1 mM EDTA) and centrifuged at 10,000 × g for 15 min at 4°C. The samples were then mixed sequentially with hydrogen peroxide; potassium hydroxide, Purpald®, and potassium periodate and were read at 540 nm.
Hepatic GSH assay
The hepatic levels of GSH were determined by using a commercialized GSH assay kit (Cayman Chemical Co., Ann Arbor, MI, USA). Cayman’s GSH assay kit utilizes a carefully optimized enzymatic recycling method which uses glutathione reductase for the quantification of GSH. The collected 1 g of liver tissues were first homogenized in 5 ml of cold buffer (i.e., 50 mM MES or phosphate, pH 6–7, containing 1 mM EDTA) and centrifuged at 10,000 × g for 15 min at 4°C followed by metaphosphoric acid deproteinization. After adding triethanolamine solution and Assay Cocktail [a mixture of MES buffer (11.25 ml), reconstituted cofactor mixture (0.45 ml), reconstituted enzyme mixture (2.1 ml), water (2.3 ml), and reconstituted DTNB (0.45 ml)], total GSH in each of the deproteinated samples was measured at 405 nm.
Hepatic MPO assay
MPO activity was measured from liver tissues using a procedure similar to that documented by Hillegas et al. . The collected 1 g of liver tissue samples were homogenized in 15 ml of potassium phosphate buffer (PB, 50 mM, pH 6.0) and centrifuged at 41,400 × g for 10 min. The pellets were then suspended in 50 mM PB containing 0.5% hexadecyl trimethyl ammonium bromide (HETAB). After three freezing and thawing cycles with sonication between cycles, the samples were next centrifuged at 41.400 × g for 10 min. Each aliquot (0.3 ml) was then added to 2.3 ml of a reaction mixture containing 50 mM PB, 0.19 mg/ml o-dianisidine, and 20 mM H2O2 solution. One unit of enzyme activity had been defined as the amount of the MPO that caused a change in the absorbance measured at 460 nm for 2 min. MPO activity had been expressed as U/g tissue.
Hepatic lipid peroxidation assay
The collected 0.5 g of liver tissue samples were homogenized with 0.01 M sodium phosphate buffer (pH 7.0) 4.5 ml. After the addition of 1% phosphoric acid 1.5 ml and 0.6% TBA solution 0.5 ml, the solution were mixed evenly, and then heated at 95°C for 1 h. Phosphorylation of lipid peroxides to be hydrolyzed by boiling, and hydrolysis products of the MDA with TBA (2-Thiobarbituric acid) to produce MDA (TBA)2. Then cool to room temperature, add 2 ml of butanol (C4H10O), and centrifuged at 2,000 × g for 15 min, take butanol layer for ELISA reader at 532 nm absorbance was measured, and TEP (1,1,3,3-tetraethoxypropane) as the standard value.
The rats were sacrificed by decapitation, and small pieces of liver tissues were placed in 10% (vol/vol) formaline solution and processed routinely by embedding in paraffin. Tissue sections (4–5 μm) were stained with Hematoxylin & Eosin (H & E) and examined under a light microscope.
The data in each experimental group were analyzed and expressed as means ± standard error of the mean (SEM). Concentrations of MPO, MDA, GSH, CAT, SOD, ALT, and AST in different groups were determined by using the Wilcoxon rank-sum test to compare the differences between two experimental groups. A P value less than 0.05 indicates statistical significance. Error bars indicates ± SEM in the figure.
Hepatic I/R induction and effects of LSTS on Qimen (LR14)
Plasma ALT and AST activities
74 ± 11.2
109 ± 7.2
843 ± 131*
1457 ± 263*
I/R + LSTS
505 ± 75*,+
549 ± 137*,+
The antioxidant activity of LSTS on Qimen (LR14) in the liver
The anti-inflammatory effect of LSTS on Qimen (LR14) in the liver
LSTS has been reported to up-regulate the gene expression of HSP70 in livers and preconditioning with LSTS on the right seventh intercostal nerve territory can protect rat livers from I/R injury. In addition, hepatic HSP70 gene expression has been demonstrated to be regulated by local heat stress over a designated skin area through a somatovisceral reflex and not by whole-body hyperthermia [21, 23].
With regard to the animal model used in this study, it is well-known that the right lobe vasculature occluded with the reperfusion of median/left lobes has been suggested to be a good model for studies on hepatic I/R injury [21, 26, 27]. In the studies on hepatic I/R injury, determinating the time for each I/R period is important. Ischemia for too-short (20 min) or too-long (90 min) time might result in little or irreversible structural and functional changes, respectively. Sinusoidal perfusion failure was found to be aggravated when the ischemic time period was prolonged to 60 min . Using 60 min of median/left lobar ischemia followed by 60 min of reperfusion as a model, our results showed distinct functional alterations (Table 1) and this provided a reproducible system for studying the protective effect of LSTS on hepatocytes from I/R injury.
The I/R injury of livers can occurred in many clinical scenarios including transplantation, trauma and hepatectomy. The main pathophysiological events during this injury comprise depletion of ATP, Kupffer cell activation with subsequent formation of ROS, formation of proinflammatory mediators, and recruitment and activation of macrophages, neutrophils, and lymphocytes. Depending on the severity of the I/R injury, the cell damage can lead to necrotic or apoptotic liver cell death, which can subsequently result in organ dysfunction [30–32]. Oxygen-derived free radicals play an important role in I/R injury in many organs like the heart and liver. The aim of these treatments is to restore the blood supply to the ischemic liver. Unfortunately, restoration of the blood flow to ischemic tissues can lead to further damages. This paradox leads to uncertain effectiveness of these strategies. The I/R injury is a complex pathophysiology with a number of contributing factors; therefore, it is difficult to obtain effective treatments or protections by targeting individual mediators or mechanisms alone. Preconditioned fasting, ischemia, pharmaceutical molecules, hyperosmolar solutions, and LSTS [23, 33–36] have been studied and appear to have the ability to increase the resistance of cells to ischemia and reperfusion events.
In this study, we clearly demonstrated that LSTS on the right Qimen (LR14) up-regulated the levels of SOD and down-regulated the level of MPO in the liver. SOD catalyses the dismutation of the superoxide anion (O2·) into H2O2, which could be transformed into H2O and O2 by CAT. In this study, we found that I/R impaired SOD activity as indicated by the markedly lowered activity when compared with the control group. But in the LSTS pretreated group, the decrease of SOD activity was significantly counteracted. HSP70 acts as a molecular chaperone, playing an essential role in mediating protein folding, assembly, transport, and degradation, helping to prevent protein denaturation and aggregation, and assisting in the refolding or removal of damaged proteins [37, 38]. It has been shown that the SOD activity and its content decrease after the I/R injury presumably via inactivation of mature and active SOD within mitochondria . It is, however, unlikely that HSP70 could prevent I/R injury induced denaturation or inactivation of mature SOD within mitochondria, because HSP70 localize in different compartments from mature and active SOD. Specifically, HSP70 distributes in cytoplasm and nucleus in both normal and stressed conditions [38, 40], while the mature and active SOD exists and acts in mitochondria . It has been clarified that HSP70 plays an essential role in keeping newly synthesized mitochondrial proteins (precursor proteins) in their correct unfolding conformation within the cytoplasm and transporting them into mitochondria [30, 31]. Therefore, one should speculate that cytoplasmic HSP70 overexpression could enhance translocation of precursor SOD into mitochondria, which then results in supplementing the pool of mature SOD within these organelles. We have demonstrated that the liver HSP70 overexpression results in improved liver tolerance to I/R injury and is associated with enhanced preservation of the SOD activity.
MPO is an enzyme stored in azurophilic granules of polymorphonuclear neutrophils and macrophages, and released into extracellular fluid in the setting of inflammatory process. MPO is involved in acute and chronic inflammatory diseases. The significant increase in the MPO activity in the liver tissue after hepatic I/R in the present study is consistent with another study . The induction of HSPs may afford protection from subsequent insults by decreasing leukocyte infiltration of post-ischemic tissues . Javadpour et al. found fewer pulmonary neutrophils and less MPO activity after aortic occlusion in rats with prior induction of HSPs via hyperthermia  or pharmacologic means . They also showed that hyperthermia prevented decrease in leukocyte rolling velocity induced by mesenteric I/R . Prior hyperthermia also decreases intestinal neutrophil infiltration and mucosal injury after intestinal ischemia . HSP70 may regulate MPO activates to mitigate the I/R injury. In additional, MPO can also serve as an indicator of inflammation and the generation of ROS, because an increase in MPO activity reflects tissue neutrophil infiltration. Neutrophils are a potential source of oxygen free radicals  and are considered to be the major effector cells involved in tissue damage that occurs in several inflammatory diseases [47, 48]. Our results show that LSTS on Qimen (LR14) may decrease MPO activates to reduce hepatic I/R injury.
Preconditioned LSTS on the right Qimen (LR14) have a beneficial effect on protecting the rat liver against I/R injury. This pre-treatment is more advantageous when compared with the pretreatment by means of whole-body hyperthermia. LSTS is an easily applicable alternative and will bring new perspectives to the clinical prevention of ischemic liver disease or liver transplantation.
Local somatothermal stimulation
Reactive oxygen species
- H & E:
Hematoxylin & Eosin.
This work was supported by the grants from National Science Concil, Taiwan, R.O.C and Veterans General Hospital, Taipei, Taiwan, R.O.C. (NSC93-2320-B-010-071, 94-2320-B-010-016, VGHUST96-G7-2, NSC102-2320-B-002-014).
- de la Monte SM, Arcidi JM, Moore GW, Hutchins GM: Midzonal necrosis as a pattern of hepatocellular injury after shock. Gastroenterology. 1984, 86 (4): 627-631.PubMedGoogle Scholar
- Yoshikawa T, Murakami M, Yoshida N, Seto O, Kondo M: Effects of superoxide dismutase and catalase on disseminated intravascular coagulation in rats. Thromb Haemost. 1983, 50 (4): 869-872.PubMedGoogle Scholar
- Arthur MJ: Reactive oxygen intermediates and liver injury. J Hepatol. 1988, 6 (1): 125-131. 10.1016/S0168-8278(88)80472-0.View ArticlePubMedGoogle Scholar
- Jungermann K, Kietzmann T: Oxygen: modulator of metabolic zonation and disease of the liver. Hepatology. 2000, 31 (2): 255-260. 10.1002/hep.510310201.View ArticlePubMedGoogle Scholar
- Lemasters JJ, Ji S, Thurman RG: Centrilobular injury following hypoxia in isolated, perfused rat liver. Science. 1981, 213 (4508): 661-663. 10.1126/science.7256265.View ArticlePubMedGoogle Scholar
- Gonzalez-Flecha B, Cutrin JC, Boveris A: Time course and mechanism of oxidative stress and tissue damage in rat liver subjected to in vivo ischemia-reperfusion. J Clin Invest. 1993, 91 (2): 456-464. 10.1172/JCI116223.View ArticlePubMedPubMed CentralGoogle Scholar
- Halliwell B: Reactive oxygen species in living systems: source, biochemistry, and role in human disease. Am J Med. 1991, 91 (3C): 14S-22S.View ArticlePubMedGoogle Scholar
- McCord JM: Oxygen-derived free radicals in postischemic tissue injury. N Engl J Med. 1985, 312 (3): 159-163. 10.1056/NEJM198501173120305.View ArticlePubMedGoogle Scholar
- Vollmar B, Glasz J, Leiderer R, Post S, Menger MD: Hepatic microcirculatory perfusion failure is a determinant of liver dysfunction in warm ischemia-reperfusion. Am J Pathol. 1994, 145 (6): 1421-1431.PubMedPubMed CentralGoogle Scholar
- Jaattela M, Wissing D, Kokholm K, Kallunki T, Egeblad M: Hsp70 exerts its anti-apoptotic function downstream of caspase-3-like proteases. EMBO J. 1998, 17 (21): 6124-6134. 10.1093/emboj/17.21.6124.View ArticlePubMedPubMed CentralGoogle Scholar
- Inoue M, Kitakoji H, Yano T, Ishizaki N, Itoi M, Katsumi Y: Acupuncture treatment for low back pain and lower limb symptoms-the relation between acupuncture or electroacupuncture stimulation and sciatic nerve blood flow. Evid Based Complement Alternat Med. 2008, 5 (2): 133-143. 10.1093/ecam/nem050.View ArticlePubMedGoogle Scholar
- Hua JS, Li LP, Zhu XM: Effects of moxibustion pretreating on SOD and MDA in the rat of global brain ischemia. J Tradit Chin Med. 2008, 28 (4): 289-292. 10.1016/S0254-6272(09)60014-5.View ArticlePubMedGoogle Scholar
- Pang Y, Wu LB, Liu DH: Acupuncture therapy for apoplectic aphasia: a systematic review. Zhongguo Zhen Jiu. 2010, 30 (7): 612-616.PubMedGoogle Scholar
- Berman BM, Langevin HM, Witt CM, Dubner R: Acupuncture for chronic low back pain. N Engl J Med. 2010, 363 (5): 454-461. 10.1056/NEJMct0806114.View ArticlePubMedGoogle Scholar
- Lee MS, Choi TY, Kang JW, Lee BJ, Ernst E: Moxibustion for treating pain: a systematic review. Am J Chin Med. 2010, 38 (5): 829-838. 10.1142/S0192415X10008275.View ArticlePubMedGoogle Scholar
- Beyerman KL, Palmerino MB, Zohn LE, Kane GM, Foster KA: Efficacy of treating low back pain and dysfunction secondary to osteoarthritis: chiropractic care compared with moist heat alone. J Manipulative Physiol Ther. 2006, 29 (2): 107-114. 10.1016/j.jmpt.2005.10.005.View ArticlePubMedGoogle Scholar
- Yeh CC, Ko SC, Huh BK, Kuo CP, Wu CT, Cherng CH, Wong CS: Shoulder tip pain after laparoscopic surgery analgesia by collateral meridian acupressure (shiatsu) therapy: a report of 2 cases. J Manipulative Physiol Ther. 2008, 31 (6): 484-488. 10.1016/j.jmpt.2008.06.005.View ArticlePubMedGoogle Scholar
- Arroyo-Morales M, Olea N, Martinez M, Moreno-Lorenzo C, Diaz-Rodriguez L, Hidalgo-Lozano A: Effects of myofascial release after high-intensity exercise: a randomized clinical trial. J Manipulative Physiol Ther. 2008, 31 (3): 217-223. 10.1016/j.jmpt.2008.02.009.View ArticlePubMedGoogle Scholar
- Pfefer MT, Cooper SR, Uhl NL: Chiropractic management of tendinopathy: a literature synthesis. J Manipulative Physiol Ther. 2009, 32 (1): 41-52. 10.1016/j.jmpt.2008.09.014.View ArticlePubMedGoogle Scholar
- Pan PJ, Chan RC, Yang AH, Chou CL, Cheng YF, Chiu JH: Protective effects of preconditioned local somatothermal stimulation on neuromuscular plasticity against ischemia–reperfusion injury in rats. J Orthop Res. 2008, 26 (12): 1670-1674. 10.1002/jor.20693.View ArticlePubMedGoogle Scholar
- Lin YH, Chiu JH, Tung HH, Tsou MT, Lui WY, Wu CW: Preconditioning somatothermal stimulation on right seventh intercostal nerve territory increases hepatic heat shock protein 70 and protects the liver from ischemia-reperfusion injury in rats. J Surg Res. 2001, 99 (2): 328-334. 10.1006/jsre.2001.6177.View ArticlePubMedGoogle Scholar
- Chiu JH, Lui WY, Chen YL, Hong CY: Local somatothermal stimulation inhibits the motility of sphincter of Oddi in cats, rabbits and humans through nitrergic neural release of nitric oxide. Life Sci. 1998, 63 (6): 413-428. 10.1016/S0024-3205(98)00291-4.View ArticlePubMedGoogle Scholar
- Chiu JH, Tsou MT, Tung HH, Tai CH, Tsai SK, Chih CL, Lin JG, Wu CW: Preconditioned somatothermal stimulation on median nerve territory increases myocardial heat shock protein 70 and protects rat hearts against ischemia-reperfusion injury. J Thorac Cardiovasc Surg. 2003, 125 (3): 678-685. 10.1067/mtc.2003.29.View ArticlePubMedGoogle Scholar
- Jiang JK, Chiu JH, Lin JK: Local somatothermal stimulation inhibits motility of the internal anal sphincter through nitrergic neural release of nitric oxide. Dis Colon Rectum. 2000, 43 (3): 381-388. 10.1007/BF02258306.View ArticlePubMedGoogle Scholar
- Hiratsuka M, Yano M, Mora BN, Nagahiro I, Cooper JD, Patterson GA: Heat shock pretreatment protects pulmonary isografts from subsequent ischemia-reperfusion injury. J Heart Lung Transplant. 1998, 17 (12): 1238-1246.PubMedGoogle Scholar
- Canada AT, Stein K, Martel D, Watkins WD: Biochemical appraisal of models for hepatic ischemia-reperfusion injury. Circ Shock. 1992, 36 (3): 163-168.PubMedGoogle Scholar
- Chiu JH, Ho CT, Wei YH, Lui WY, Hong CY: In vitro and in vivo protective effect of honokiol on rat liver from peroxidative injury. Life Sci. 1997, 61 (19): 1961-1971. 10.1016/S0024-3205(97)00836-9.View ArticlePubMedGoogle Scholar
- Hillegass LM, Griswold DE, Brickson B, Albrightson-Winslow C: Assessment of myeloperoxidase activity in whole rat kidney. J Pharmacol Methods. 1990, 24 (4): 285-295. 10.1016/0160-5402(90)90013-B.View ArticlePubMedGoogle Scholar
- Koo A, Komatsu H, Tao G, Inoue M, Guth PH, Kaplowitz N: Contribution of no-reflow phenomenon to hepatic injury after ischemia-reperfusion: evidence for a role for superoxide anion. Hepatology. 1992, 15 (3): 507-514. 10.1002/hep.1840150325.View ArticlePubMedGoogle Scholar
- Deshaies RJ, Koch BD, Werner-Washburne M, Craig EA, Schekman R: A subfamily of stress proteins facilitates translocation of secretory and mitochondrial precursor polypeptides. Nature. 1988, 332 (6167): 800-805. 10.1038/332800a0.View ArticlePubMedGoogle Scholar
- Wienhues U, Neupert W: Protein translocation across mitochondrial membranes. Bioessays. 1992, 14 (1): 17-23. 10.1002/bies.950140105.View ArticlePubMedGoogle Scholar
- Jaeschke H: Molecular mechanisms of hepatic ischemia-reperfusion injury and preconditioning. Am J Physiol Gastrointest Liver Physiol. 2003, 284 (1): G15-G26.View ArticlePubMedGoogle Scholar
- Liu Z, Xu Z, Shen W, Li Y, Zhang J, Ye X: Effect of pharmacologic preconditioning with tetrandrine on subsequent ischemia/reperfusion injury in rat liver. World J Surg. 2004, 28 (6): 620-624.View ArticlePubMedGoogle Scholar
- Oreopoulos GD, Wu H, Szaszi K, Fan J, Marshall JC, Khadaroo RG, He R, Kapus A, Rotstein OD: Hypertonic preconditioning prevents hepatocellular injury following ischemia/reperfusion in mice: a role for interleukin 10. Hepatology. 2004, 40 (1): 211-220. 10.1002/hep.20281.View ArticlePubMedGoogle Scholar
- Takahashi Y, Tamaki T, Tanaka M, Konoeda Y, Kawamura A, Katori M, Kakita A: Efficacy of heat-shock proteins induced by severe fasting to protect rat livers preserved for 72 hours from cold ischemia/reperfusion injury. Transplant Proc. 1998, 30 (7): 3700-3702. 10.1016/S0041-1345(98)01201-9.View ArticlePubMedGoogle Scholar
- Vajdova K, Heinrich S, Tian Y, Graf R, Clavien PA: Ischemic preconditioning and intermittent clamping improve murine hepatic microcirculation and Kupffer cell function after ischemic injury. Liver Transpl. 2004, 10 (4): 520-528. 10.1002/lt.20126.View ArticlePubMedGoogle Scholar
- Latchman DS: Heat shock proteins and cardiac protection. Cardiovasc Res. 2001, 51 (4): 637-646. 10.1016/S0008-6363(01)00354-6.View ArticlePubMedGoogle Scholar
- Parsell DA, Lindquist S: The function of heat-shock proteins in stress tolerance: degradation and reactivation of damaged proteins. Annu Rev Genet. 1993, 27: 437-496. 10.1146/annurev.ge.27.120193.002253.View ArticlePubMedGoogle Scholar
- Russell WJ, Jackson RM: MnSOD protein content changes in hypoxic/hypoperfused lung tissue. Am J Respir Cell Mol Biol. 1993, 9 (6): 610-616. 10.1165/ajrcmb/9.6.610.View ArticlePubMedGoogle Scholar
- Knowlton AA, Kapadia S, Torre-Amione G, Durand JB, Bies R, Young J, Mann DL: Differential expression of heat shock proteins in normal and failing human hearts. J Mol Cell Cardiol. 1998, 30 (4): 811-818. 10.1006/jmcc.1998.0646.View ArticlePubMedGoogle Scholar
- Weisiger RA, Fridovich I: Superoxide dismutase, organelle specificity. J Biol Chem. 1973, 248 (10): 3582-3592.PubMedGoogle Scholar
- Javadpour M, Kelly CJ, Chen G, Bouchier-Hayes DJ: Herbimycin-A attenuates ischaemia-reperfusion induced pulmonary neutrophil infiltration. Eur J Vasc Endovasc Surg. 1998, 16 (5): 377-382. 10.1016/S1078-5884(98)80003-8.View ArticlePubMedGoogle Scholar
- Javadpour M, Kelly CJ, Chen G, Stokes K, Leahy A, Bouchier-Hayes DJ: Thermotolerance induces heat shock protein 72 expression and protects against ischaemia-reperfusion-induced lung injury. Br J Surg. 1998, 85 (7): 943-946. 10.1046/j.1365-2168.1998.00722.x.View ArticlePubMedGoogle Scholar
- Chen G, Kelly C, Stokes K, Wang JH, Leahy A, Bouchier-Hayes D: Induction of heat shock protein 72 kDa expression is associated with attenuation of ischaemia-reperfusion induced microvascular injury. J Surg Res. 1997, 69 (2): 435-439. 10.1006/jsre.1997.5059.View ArticlePubMedGoogle Scholar
- Stojadinovic A, Kiang J, Smallridge R, Galloway R, Shea-Donohue T: Induction of heat-shock protein 72 protects against ischemia/reperfusion in rat small intestine. Gastroenterology. 1995, 109 (2): 505-515. 10.1016/0016-5085(95)90339-9.View ArticlePubMedGoogle Scholar
- Weiss SJ, Ward PA: Immune complex induced generation of oxygen metabolites by human neutrophils. Journal of immunology. 1982, 129 (1): 309-313.Google Scholar
- Heinzelmann M, Mercer-Jones MA, Passmore JC: Neutrophils and renal failure. Am J Kidney Dis. 1999, 34 (2): 384-399. 10.1016/S0272-6386(99)70375-6.View ArticlePubMedGoogle Scholar
- Zimmerman BJ, Grisham MB, Granger DN: Role of oxidants in ischemia/reperfusion-induced granulocyte infiltration. Am J Physiol. 1990, 258 (2 Pt 1): G185-G190.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6882/14/18/prepub
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