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纸质出版日期:2015
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王付, 程秀娟, 王帮民, 等. 甘遂半夏汤对大鼠肝功能及形态学的影响[J]. 中国实验方剂学杂志, 2015,21(8):160-164.
WANG Fu, CHENG Xiu-juan, WANG Bang-min, et al. Effect of Gansui Banxia Tang on Functions and Morphology in Rats Liver[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(8): 160-164.
王付, 程秀娟, 王帮民, 等. 甘遂半夏汤对大鼠肝功能及形态学的影响[J]. 中国实验方剂学杂志, 2015,21(8):160-164. DOI: 10.13422/j.cnki.syfjx.2015080160.
WANG Fu, CHENG Xiu-juan, WANG Bang-min, et al. Effect of Gansui Banxia Tang on Functions and Morphology in Rats Liver[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(8): 160-164. DOI: 10.13422/j.cnki.syfjx.2015080160.
目的: 探讨甘遂半夏汤水煎液对正常大鼠肝脏的慢性毒性作用。方法: 将80只SD大鼠随机分为甘遂半夏汤高、中、低剂量组(37
18.5
9.25 g·kg-1)及正常组
每组20只
各组大鼠采用等体积不等浓度ig
ig体积均为0.02 mL·g-1。实验组ig给药
正常组ig给予蒸馏水。给药90 d。最后1次给药后禁食15 h
各组随机抽取一半大鼠
取血
采用全自动生化分析仪检测肝功能指标丙氨酸氨基转移酶(ALT)
天门冬氨酸氨基转移酶(AST)
AST/ALT
总胆红素(TBIL)和直接胆红素(DBIL)
及血脂指标胆固醇(CHO)
甘油三酯(TG)
高密度脂蛋白(HDL)
低密度脂蛋白(LDL);取肝
HE染色观察大体形态和组织学形态。剩余动物停药后继续观察2周
重复以上检查指标。结果: 给药期
与正常组比较
甘遂半夏汤高剂量组ALT
AST
AST/ALT
TBIL和DBIL均明显升高(P<0.01)
中剂量组ALT
AST
DBIL(P<0.05)和AST/ALT均明显升高(P<0.01)
低剂量组无显著变化;与正常组比较
各剂量组CHO
TG
HDL
LDL无显著性变化;随着剂量增大
肝脏组织病理变化逐渐加重。恢复期
各组大鼠各项检测指标及肝脏组织学形态无显著差异。结论: 长期服用甘遂半夏汤可导致大鼠肝损伤
对大鼠肝功能及肝组织形态学的影响存在着剂量依赖性
小剂量长期使用影响较小
随着剂量的增加
影响的程度逐渐加重
但损伤具有可逆性。
Objective: To explore the chronic toxicity of Gansui Banxia Tang (GBT) on normal rat liver. Method: Eighty healthy SD rats were randomly divided into four groups:the normal group
the high-
middle-
and low-dose GBT groups (37
18.5
9.25 g·kg-1) of 20 in each group. The corresponding medicines at 0.02 mL·g-1were intragastrically administrated to rats for 90 days. After the last dose
blood samples of the half rats from each group were collected. The heart functions indexes including alanine aminotransferase (ALT)
aspartate aminotransferase (AST)
the ratio of AST/ALT
total bilirubin (TBIL)
direct bilirubin (DBIL)
and the blood lipid indexes including cholesterol (CHO)
triglyceride (TG)
high density lipoprotein (HDL)
low density lipoprotein (LDL) were detected. The morphology and histology of the liver were observed by HE staining. The remaining rats in each group were observed continuously for two weeks
and the above indexes were detected again. Result: In medicine taking
compared with the control group
the ALT
AST
AST/ALT
TBIL and DBIL had significant changes in high-dose GBT group (P<0.01)
the ALT
AST
DBIL (P<0.05) and AST/ALT(P<0.01) had significant changes in the middle-dose GBT group. The above indexes had no significant changes in the low-dose GBT group. The CHO
TG
HDL and LDL had no significant changes in all dose groups. The liver histopathological changes are gradually aggravated with the increase of the dose. While during the following observation
all the above indexes had no significant changes in all dose GBT groups. Conclusion: GBT has good effect on liver function and morphology of rats in a dose-dependent manner by long-term medication. Small dosage has little influence
the influence degree aggravates gradually as the increase of the dose
while the damage is reversible.
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