皖西学院学报
皖西學院學報
환서학원학보
JOURNAL OF WANXI UNIVERSITY
2012年
5期
92-94
,共3页
徐茂红%王菲菲%高燕%陈晓芳%李光燕%汪洋奎%方士英
徐茂紅%王菲菲%高燕%陳曉芳%李光燕%汪洋奎%方士英
서무홍%왕비비%고연%진효방%리광연%왕양규%방사영
葛根黄酮CCl4%诱导%肝损伤%大别山区
葛根黃酮CCl4%誘導%肝損傷%大彆山區
갈근황동CCl4%유도%간손상%대별산구
total pueraria flavonoids CCl4 liver injury protective effect Dabie Mountains
研究大别山区葛根总黄酮(TPF)对CCl4诱导小鼠化学性肝损伤的保护作用及可能的作用机制。采用1次性腹腔注射(ip)0.1%CCl4花生油溶液(10ml/kg)建立小鼠化学性肝损伤模型。TPF连续灌胃(ig)14d后摘眼球取血,分离血清,测定血清中丙氨酸氨基转移酶(ALT)和天门冬氨酸氨基转移酶(AST)活性;剖腹取肝,制备10%肝匀浆,测定肝组织中超氧化物歧化酶(SOD)、丙二醛(MDA)、干扰素-γ(IFN-γ)、肿瘤坏死因子-α(TNF-α)活性;进行肝组织病理切片,观察肝组织病理学变化。结果显示TPF能降低CCl4诱导的化学性肝损伤小鼠血清中ALT、AST和肝匀浆中MDA、IFI-γ、TNF-α的活性及增强肝匀浆中SOD的活力。其作用机制可能与抗氧化和降低肝组织中IFN-γ、TNF-α水平有关。
研究大彆山區葛根總黃酮(TPF)對CCl4誘導小鼠化學性肝損傷的保護作用及可能的作用機製。採用1次性腹腔註射(ip)0.1%CCl4花生油溶液(10ml/kg)建立小鼠化學性肝損傷模型。TPF連續灌胃(ig)14d後摘眼毬取血,分離血清,測定血清中丙氨痠氨基轉移酶(ALT)和天門鼕氨痠氨基轉移酶(AST)活性;剖腹取肝,製備10%肝勻漿,測定肝組織中超氧化物歧化酶(SOD)、丙二醛(MDA)、榦擾素-γ(IFN-γ)、腫瘤壞死因子-α(TNF-α)活性;進行肝組織病理切片,觀察肝組織病理學變化。結果顯示TPF能降低CCl4誘導的化學性肝損傷小鼠血清中ALT、AST和肝勻漿中MDA、IFI-γ、TNF-α的活性及增彊肝勻漿中SOD的活力。其作用機製可能與抗氧化和降低肝組織中IFN-γ、TNF-α水平有關。
연구대별산구갈근총황동(TPF)대CCl4유도소서화학성간손상적보호작용급가능적작용궤제。채용1차성복강주사(ip)0.1%CCl4화생유용액(10ml/kg)건립소서화학성간손상모형。TPF련속관위(ig)14d후적안구취혈,분리혈청,측정혈청중병안산안기전이매(ALT)화천문동안산안기전이매(AST)활성;부복취간,제비10%간균장,측정간조직중초양화물기화매(SOD)、병이철(MDA)、간우소-γ(IFN-γ)、종류배사인자-α(TNF-α)활성;진행간조직병리절편,관찰간조직병이학변화。결과현시TPF능강저CCl4유도적화학성간손상소서혈청중ALT、AST화간균장중MDA、IFI-γ、TNF-α적활성급증강간균장중SOD적활력。기작용궤제가능여항양화화강저간조직중IFN-γ、TNF-α수평유관。
The protective effects and the mechanisms were studied about TPF from Dabie Mountains on chemical liver injury in mice induced by CCl4. The mouse was Injected 0. 1% CCl4 solution dissolved in peanut oil (10 ml/kg) into it's abdominal cavity to set animal models of chemical liver injury. The blood samples were drawn out to determine ALT and AST by intragastric administration with TPF for 14d. The liver tissue homogenates were drawn for the determination of IFN-γ/and TNF-α. And the liver histopathology was studied with morphological method. The results showed that, compared with model group, TPF could decrease ALT, AST in serum and MDA, IFN-γ, TNF-α in liver, and increase the activity of SOD in liver. TPF could protect against chemical liver injury induced by CCl4 in mice. The mechanisms may be related to the antioxidant activity of TPF and it's effect to decrease the IFN-γ and TNF-α level in liver.