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纸质出版:2012
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李果,夏锋,吴林,姚超,钱程,别平.β肾上腺素能受体兴奋对大鼠急性肝损伤的影响[J].陆军军医大学学报(原第三军医大学学报),2012,34(09):809-812.
Li Guo,Xia Feng,Wu Lin,Yao Chao,Qian Cheng,Bie Ping.Effect of stimulation of β-adrenoceptor on acute liver injury in rats[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(09):809-812.
目的 探讨β肾上腺素能受体兴奋对大鼠急性肝损伤的影响。 方法 使用异丙肾上腺素兴奋β肾上腺素能受体,在不同的用药剂量(1、10、100 mg/kg)和不同的损伤时相点(24、48、72、96 h)以及使用普萘洛尔抑制β肾上腺素能受体兴奋的情况下,检测肝功能指标[谷丙转氨酶(ALT)、谷草转氨酶(AST)、白蛋白(Alb)和总胆红素(TBil)],观察组织病理学变化,探讨β肾上腺素能受体兴奋对大鼠急性肝损伤的影响。 结果 大鼠肝损伤程度随着异丙肾上腺素剂量的加大而加重[ALT(IU/L):对照组(336.2±140.5),1 mg/kg组(603.7±239.7),10 mg/kg组(838.6±448.5),100 mg/kg组(1 571.5±714.7),P0.05];在急性肝损伤后第48小时对照组与实验组各项肝功能指标均有统计学差异[ALT(IU/L):(290.8±153.9)、(636.0±385.2),P0.05;AST(IU/L):(521.0±296.8)、(2 289.1±1 361.5),P0.05;Alb(g/L):(28.3±1.3)、(25.2±1.5),P0.05;TBil(μmol/L):(4.1±1.2)、(24.8±16.9),P0.05];应用普萘洛尔抑制β肾上腺素能受体兴奋,能有效防止大鼠急性肝损伤加重[ALT:兴奋组(606.0±154.9) IU/L,抑制组(210.0±176.1) IU/L,P0.05]。 结论 β肾上腺素能受体的兴奋能有效调控大鼠急性肝损伤的进程。
Objective To determine the effect of stimulation of β-adrenoceptor by isoprenaline injection on acute liver injury in rats. Methods Effect of intraperitoneal injection of isoprenaline pretreatment to stimulate β-adrenoceptor at different doses (1
10 and 100 mg/kg)
and for different time periods after acute liver injury (24
48
72 and 96 h)
or of propranolol to inhibit β-adrenoceptor
was detected on the liver function index in blood serum and pathological examination. Results With the increase of isoprenaline dose
acute liver injury became more serious (ALT: control group 336.2±140.5 IU/L
1 mg/kg group 603.7±239.7 IU/L
10 mg/kg group 838.6±448.5 IU/L
100 mg/kg group 1571.5±714.7 IU/L
P0.05). Each index of liver function was statistically different between control group and stimulus group at 48 h after acute liver injury (ALT: 290.8±153.9
636.0±385.2 IU/L
P0.05; AST: 521.0±296.8
2 289.1±1 361.5 IU/L
P0.05; Alb: 28.3±1.3
25.2±1.5 g/L
P0.05; TBil: 4.1±1.2
24.8±16.9 μmol/L
P0.05). Meanwhile
propranolol inhibited β-adrenoceptor activation
and effectively prevented acute liver injury becoming more serious (ALT: stimulus group 606.0±154.9 IU/L
inhibition group 210.0±176.1 IU/L
P0.05). Conclusion Stimulation of β-adrenoceptor may effectively regulate the process of acute liver injury in rats.
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