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纸质出版日期:2017
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冯果, 李玮, 何新, 等. 苗族药了哥王不同提取物对正常大鼠肝毒性的影响[J]. 中国实验方剂学杂志, 2017,23(11):96-102.
FENG Guo, LI Wei, HE Xin, et al. Effects of Different Extracts of Miao Medicine Root on Hepatotoxicity in Normal Rats[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(11): 96-102.
冯果, 李玮, 何新, 等. 苗族药了哥王不同提取物对正常大鼠肝毒性的影响[J]. 中国实验方剂学杂志, 2017,23(11):96-102. DOI: 10.13422/j.cnki.syfjx.2017110096.
FENG Guo, LI Wei, HE Xin, et al. Effects of Different Extracts of Miao Medicine Root on Hepatotoxicity in Normal Rats[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(11): 96-102. DOI: 10.13422/j.cnki.syfjx.2017110096.
目的:考察了哥王不同提取物对正常大鼠肝毒性的影响,并探讨其作用机制。方法:选用SD大鼠72只,随机分成空白组、乙醇提取物组、石油醚提取物组、乙酸乙酯提取物组、正丁醇提取物组和水部位提取物组,每组12只。不同给药组连续灌胃给药2周,每隔2日称量大鼠体重,于第15天,每组随机取6只,麻醉后腹主动脉取血,离心血液,取血清测定丙氨酸氨基转移酶(ALT),天门冬氨酸氨基转移酶(AST),碱性磷酸酶(ALP),总胆红素(T-BIL),总蛋白(TP),白蛋白(ALB),血糖(GLU),总胆固醇(CHOL),肌酐(Cr)。取肝组织,称其质量,计算脏器系数,并留取肝组织作病理学检查。每组余下的6只大鼠于第15天停止给药,正常供给饲料与水,恢复2周,观察大鼠恢复情况,于第28天进行上述相同指标的检测。结果:给药2周后,与空白组比较,乙醇提取物组和乙酸乙酯提取物组大鼠的肝脏系数明显增大(P<0.05)。乙醇提取物组血清中ALT,AST,GLB明显升高,白蛋白/球蛋白(A/G),TP和ALB明显降低(P<0.05);乙酸乙酯提取物组血清中ALP,T-BIL,GLU明显升高,A/G,TP和ALB明显降低(P<0.05);石油醚提取物组血清中AST,AST/ALT,ALP,GLU明显升高,T-BIL,A/G,TP和ALB明显降低(P<0.05,P<0.01);正丁醇提取物组血清中AST/ALT,T-BIL明显升高,A/G明显降低(P<0.05,P<0.01);水部位提取物组血清中A/G明显降低(P<0.05);乙醇提取物组、乙酸乙酯提取物组和石油醚提取物组大鼠肝组织能观察到不同程度的炎细胞浸润,出现一定的肝细胞脂肪变性和局灶性肝细胞坏死,其他组少见。停药恢复2周后,各组肝脏系数均接近于空白组;各组血清中肝功能生化指标基本恢复到空白组水平;各组大鼠肝组织细胞结构清晰,少见炎细胞浸润,未见脂肪变性和肝细胞坏死。结论:苗族药了哥王乙醇提取物组、乙酸乙酯提取物组对肝损伤较大,具有明显的肝毒性;石油醚提取物组对肝也有一定的损伤,但比乙醇提取物组和乙酸乙酯提取物组损伤程度小;正丁醇提取物组毒性较小,水部位提取物组无毒性;停药2周恢复后,各组大鼠反映肝功能的生化指标基本恢复到空白组水平,大鼠的肝损伤明显的减轻,表明了哥王的肝毒性具有一定的可逆性。
Objective: To study the effects of different extracts from Wikstroemia indica root on the hepatotoxicity in rats. Method: Seventy-two SD rats were randomly divided into blank control group
ethanol extract group
petroleum ether extract group
ethyl acetate extract group
n-butanol extract group and water extract group
with 12 rats in each group. Different drug groups were intragastrically administrated with drugs for two weeks
and the rats' body weight was measured once every two days. On the fifteenth day
six rats were randomly selected from each group
and anaesthetized with 3% pentobarbital sodium
and their blood was collected from aorta abdominalis. After blood centrifugation
the alanine aminotransferase (ALT)
aspartate aminotransferase (AST)
alkaline phosphatase (ALP)
total bilirubin (T-BIL)
total protein (TP)
albumin (ALB)
blood glucose (GLU)
total cholesterol (CHOL)
and creatinine (Cr) in serum were detected. Their livers were collected and weighed
and the organ index was calculated. The hepatic histopathology was examined. Then the remaining six rats in each group were given no drug but fed with normal food and water for two weeks to observe their recovery. The above indexes were detected on the twenty-eighth day. Result: Compared with control group
the liver coefficients of ethanol extract group and ethyl acetate extract group increased significantly after two weeks (P<0.05). The serum levels of ALT
AST
GLB were increased
and A/G
TP and ALB were decreased (P<0.05) in ethanol extract group. The serum levels of ALP
T-BIL
GLU were increased
and A/G
TP and ALB were decreased (P<0.05) in ethyl acetate extract group. The serum levels of AST
AST/ALT
ALP
GLU were increased
T-BIL
ALB
TP and A/G were decreased in petroleum ether extract group (P<0.05
P<0.01). The serum levels of AST/ALT
T-BIL were increased and A/G decreased (P<0.05
P<0.01) in extract of butanol. Only A/G decreased in the serum of water extract group (P<0.05). The rat liver tissues of ethanol extract group
ethyl acetate extract group and petroleum ether extract group showed different degrees of inflammatory cell infiltration
certain fatty degeneration of liver cells and focal necrosis of liver cells
which were rare in other rare group. After the drug withdrawal for two weeks
the liver coefficient of each group was close to that of blank control group. The biochemical indexes of liver function in each group were recovered to the level of blank group
and there was no significant difference. The liver tissue cells of each group showed a clear structure
with rare inflammatory cells infiltration and no fatty degeneration and necrosis of liver cells. Conclusion: The ethanol extract group and the ethyl acetate extracted group of Miao medicine W. indica root have a greater damage to the liver
with obvious hepatotoxicity. The petroleum ether extract group also shows a certain injury to liver
which however is lower than that of the ethanol extract group and the ethyl acetate extracted group. The n-butanol extract group shows a lower toxicity
and the water extract group shows no toxicity. After recovery for two weeks
the biochemical indexes of liver function of rats in each group were almost recovered to the level of the blank group
and the liver injury of rats was significantly reduced
which indicated that the hepatotoxicity of W. indica root had a certain reversibility.
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