Czerny Christoph, Theruvath Tom P, Maldonado Eduardo N, Lehnert Mark, Marzi Ingo, Zhong Zhi, Lemasters John J
Center for Cell Death, Injury & Regeneration, Departments of Pharmaceutical & Biomedical Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
HPB Surg. 2012;2012:641982. doi: 10.1155/2012/641982. Epub 2012 Jun 27.
Hemorrhagic shock leads to hepatic hypoperfusion and activation of mitogen-activated stress kinases (MAPK) like c-Jun N-terminal kinase (JNK) 1 and 2. Our aim was to determine whether mitochondrial dysfunction leading to hepatic necrosis and apoptosis after hemorrhage/resuscitation (H/R) was dependent on JNK2. Under pentobarbital anesthesia, wildtype (WT) and JNK2 deficient (KO) mice were hemorrhaged to 30 mm Hg for 3 h and then resuscitated with shed blood plus half the volume of lactated Ringer's solution. Serum alanine aminotransferase (ALT), necrosis, apoptosis and oxidative stress were assessed 6 h after resuscitation. Mitochondrial polarization was assessed by intravital microscopy. After H/R, ALT in WT-mice increased from 130 U/L to 4800 U/L. In KO-mice, ALT after H/R was blunted to 1800 U/l (P < 0.05). Necrosis, caspase-3 activity and ROS were all substantially decreased in KO compared to WT mice after H/R. After sham operation, intravital microscopy revealed punctate mitochondrial staining by rhodamine 123 (Rh123), indicating normal mitochondrial polarization. At 4 h after H/R, Rh123 staining became dim and diffuse in 58% of hepatocytes, indicating depolarization and onset of the mitochondrial permeability transition (MPT). By contrast, KO mice displayed less depolarization after H/R (23%, P < 0.05). In conclusion, JNK2 contributes to MPT-mediated liver injury after H/R.
失血性休克会导致肝脏灌注不足,并激活丝裂原活化应激激酶(MAPK),如c-Jun氨基末端激酶(JNK)1和2。我们的目的是确定出血/复苏(H/R)后导致肝脏坏死和凋亡的线粒体功能障碍是否依赖于JNK2。在戊巴比妥麻醉下,将野生型(WT)和JNK2缺陷型(KO)小鼠出血至30 mmHg并持续3小时,然后用回输的血液加一半体积的乳酸林格氏液进行复苏。复苏6小时后评估血清丙氨酸氨基转移酶(ALT)、坏死、凋亡和氧化应激。通过活体显微镜评估线粒体极化。H/R后,WT小鼠的ALT从130 U/L增加到4800 U/L。在KO小鼠中,H/R后的ALT降至1800 U/L(P < 0.05)。与WT小鼠相比,H/R后KO小鼠的坏死、caspase-3活性和活性氧均显著降低。假手术后,活体显微镜显示罗丹明123(Rh123)对线粒体进行点状染色,表明线粒体极化正常。H/R后4小时,58%的肝细胞中Rh123染色变暗淡且弥散,表明线粒体通透性转换(MPT)去极化和开始。相比之下,KO小鼠在H/R后去极化较少(23%,P < 0.05)。总之,JNK2促成了H/R后MPT介导的肝损伤。