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作 者:史欣[1] 刘书花[1] 焦清海[1] 武向丽[2]
机构地区:[1]邯郸市第一医院重症医学科,邯郸056002 [2]邯郸市中心医院药学部,邯郸056001
出 处:《中药药理与临床》2015年第3期64-66,共3页Pharmacology and Clinics of Chinese Materia Medica
基 金:邯郸市第一医院重症医学科研究基金
摘 要:目的:研究番茄红素(Lycopene,LP)对大鼠肝脏局部缺血再灌注损伤的保护作用,并探讨其作用机制。方法:通过夹闭肝门静脉和肝动脉60min后去夹恢复血流的方法制作肝脏局部缺血再灌注模型,选取96只模型大鼠随机分为肝缺血再灌注模型对照组、番茄红素(5、10、20、40mg/kg)治疗组,复方丹参滴丸(135mg/kg)阳性对照组,并另取16只同龄大鼠作为假手术组;术后灌胃给药治疗4周,每天一次。4周后,通过生化分析仪测定各组大鼠血清中谷丙转氨酶(ALT)、谷草转氨酶(AST)、碱性磷酸酶(ALP)活性,并通过紫外-可见分光光度计测定血清中丙二醛(MDA)含量以及总抗氧化能力(T-AOC)水平;检测肝脏组织中超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)、过氧化氢酶(CAT)活性;并通过HE染色观察肝脏组织病理学改变。结果:较缺血再灌注模型对照组,番茄红素(10、20、40mg/kg)治疗组大鼠血清中ALT、AST活性和MDA含量显著降低;番茄红素(20、40mg/kg)治疗组大鼠血清中ALP活性显著降低,T-AOC水平显著升高,肝脏组织中SOD和CAT活性显著升高;番茄红素(40mg/kg)治疗组大鼠肝脏组织中GSH-Px活性显著升高;番茄红素各治疗组肝组织病理性改变出现不同程度的改善,其中以番茄红素40mg/kg治疗组效果最为显著。结论:番茄红素对大鼠肝脏缺血再灌注损伤具有剂量依赖性的保护作用,其作用可能与番茄红素能够有效改善抗氧化酶活性、抑制氧化应激损伤、改善肝功能有关。Objective: To investigate the protection and mechanism of lycopene against focal hepatic ischemia-reperfusion injury in rats. Methods: 96 focal hepatic isehemia-reperfusion rat models were randomly devided into six groups: hepatic ischemia-reperfusion control group, LP (5, 10, 20 and 40 mg/kg) treated groups and Fufangdanshendiwan( 135 mg/kg) treated group; and selected another 16 same-aged rats as sham operation group. The drugs were given by intragastrie administration for 4 months, once a day. The activity of ALT, AST, ALP and the con- tent of MDA in serum were determined, and the level of T-AOC was also determined; the activity of SOD, GSH-Px, CAT in hepar were de- termined; and the histopathological changes of the hepatic tissue observed by HE staining. Results: Compared with the hepatic ischemia- reperfusion control group, the activity of ALT, AST and the content of MDA in the serum of LP ( 10, 20 and 40 mg/kg) treated groups were significantly decreased( P 〈 0.05, P 〈 0.01 ) ; the activity of ALP in serum of LP (20 and 40 mg/kg) treated groups were significantly de- creased(P 〈0.05, P 〈0.01 ), the level of T-AOC were signifieandy increased( P 〈 0.05, P 〈 0.01 ), the activity of SOD, CAT in hepar were significantly increased( P 〈0.05, P 〈0.01 ) ; the activity of GSH-Px in hepar of LP 40 mg/kg treated group was significantly increased ( P 〈 0.01 ) ; the hepatic tissue histopathologieal changes of LP groups were significantly improved, especially the LP 40 mg/kg group. Con- clusion: LP had dose-dependent protective effects against hepatic isehemia-reperfusion injury in rats, which perhaps related to its effects of enhanceing the activity of antioxidant enzymes, redueeing the oxidative stress and improveing hepatic function.
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