Hypothalamic AMPK-induced autophagy ameliorates hypercatabolism in septic rats by regulating POMC expression

被引:18
作者
Cao, Chun [1 ]
Gao, Tao [2 ]
Cheng, Yan [1 ]
Cheng, Minhua [1 ]
Su, Ting [1 ]
Xi, Fengchan [2 ]
Wu, Cuili [2 ]
Yu, Wenkui [1 ]
机构
[1] Nanjing Univ, Affliated Drum Tower Hosp, Dept Intens Care Unit, Med Sch, Nanjing 210002, Jiangsu, Peoples R China
[2] Nanjing Univ, Jinling Hosp, Dept Gen Surg, Med Sch, Nanjing 210002, Jiangsu, Peoples R China
关键词
Hypercatabolism; Sepsis; Hypothalamic AMPK; Autophagy; POMC; ACTIVATED PROTEIN-KINASE; FOOD-INTAKE; AGRP NEURONS; LEPTIN; PROOPIOMELANOCORTIN; GLUCOSE; NEUROPEPTIDES; INFLAMMATION; SEPSIS; NPY;
D O I
10.1016/j.bbrc.2018.02.184
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypercatabolism plays a critical role in the pathogenesis of post-critical care debility in critical patients. Central nervous system may exerte a critical role in the regulation of hypercatabolism. However, little is known about the exact mechanisms of the central role. Here, we reported that actived hypothalamic AMP-activated protein kinase (AMPK)-induced autophagy modulated the expression of POMC to ameliorate hypercatabolism in septic rats. Firstly, rats were i.c.v. injected with the lentiviral vector containing shRNA against POMC. Two weeks after injections, rats were intraperitoneally injected with LPS or saline. Twenty-four hours later, blood, skeletal muscle and hypothalamus tissues were obtained. Hypercatabolism markers and neuropeptides expression were detected. Then, rats were injected with AICAR or saline into third ventricle and promptly intraperitoneally injected with LPS or saline. Twenty-four hours after infection, blood, skeletal muscle and hypothalamus tissues were obtained. Hypercatabolism, hypothalamic AMPK-induced autophagy markers and neuropeptides expression were also detected. Results showed that sepsis would decrease the level of hypothalamic autophagy accompany with the alterations of POMC expression and hypercatabolism. Knocking out hypothalamus POMC expression could significantly ameliorate hypercatabolism. Moreover, Central activation of AMPK-induced autophagy pathway via third ventricle injection of AICAR, an AMPK activator, could efficiently ameliorate hypercatabolism as well as attenuate the elevated POMC expression rather than other neuropeptides. Taken together, these results suggested that hypothalamic AMPK-autophagy pathway as a regulatory pathway for POMC expression was essential for hypercatabolism during sepsis. And hypothalamic AMPK-autophagy activation could attenuate the POMC expression to ameliorate hypercatabolism. Pharmaceuticals with the ability of activating hypothalamic AMPK-autophagy pathway may be a therapeutic potential for hypercatabolism in septic patients. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:1089 / 1096
页数:8
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