Folashade Olabinri P, Boyenle Ibrahim Damilare, Oyedeji Tolulope A, Ojeniyi Fiyinfoluwa Demilade, Damilare Adisa Ayobami, Ehigie Leonard O, Ehigie Adeola Folasade
Membrane Biochemistry and Biophysics Research Laboratory, Department of Biochemistry, Ladoke Akintola University of Technology, Ogbomoso 210214, Nigeria.
College of Health Sciences, Crescent University Abeokuta, Abeokuta 111105, Nigeria.
Chin Herb Med. 2023 Oct 16;16(1):113-120. doi: 10.1016/j.chmed.2023.06.002. eCollection 2024 Jan.
To assess acute toxicity, the and effects of methanol and ethyl acetate extracts (JME and JEE) of Jatonik polyherbal mixture on some mitochondria-related parameters and their effect on the activity of some liver enzymes.
Acute toxicity of JME and JEE was determined using Lorke's method. and opening of the mitochondrial membrane permeability transition pore (MMPT pore) was spectrophotometrically assayed. Production of malondialdehyde (MDA) as an index of lipid peroxidation and the activity of mitochondrial ATPase was evaluated and and the effect of JME and JEE on the activity of liver enzymes such as alkaline phosphatase (ALP), aspartate and alanine aminotransferase (AST and ALT) and gamma-glutamyl transferase (GGT) was also investigated.
JME had an LD of 3 808 mg/kg b.w whereas JEE had an LD greater than 5 000 mg/kg b.w. of rats. After the rats have been fed with both extracts, a photomicrograph of a piece of liver tissue showed no apparent symptoms of toxicity. From the and studies, both extracts prompted intact mitochondria to open their MMPT pores. When compared to the control, lipid peroxide product release and ATPase activity were significantly increased ( < 0.05) and . The activities of AST, ALT, and GGT were all reduced at 50 mg/kg when treated with JME, but the activity of AST was considerably enhanced when treated with JEE ( < 0.05). The results revealed that both JME and JEE of the Jatonik polyherbal mixture had low toxicity, profound MMPTpore induction, and enhanced ATPase activity, but an increased MDA production.
Jatonik extracts may be a promising target for drug development in diseases where there is dysregulation of apoptosis, however, further studies are needed to better clarify the molecular mechanism involved in these phenomena.
评估Jatonik多草药混合物的甲醇提取物和乙酸乙酯提取物(JME和JEE)的急性毒性、对某些线粒体相关参数的影响及其对某些肝脏酶活性的作用。
采用洛克方法测定JME和JEE的急性毒性。用分光光度法测定线粒体膜通透性转换孔(MMPT孔)的开放情况。评估丙二醛(MDA)的产生作为脂质过氧化的指标以及线粒体ATP酶的活性,并且还研究了JME和JEE对碱性磷酸酶(ALP)、天冬氨酸和丙氨酸转氨酶(AST和ALT)以及γ-谷氨酰转移酶(GGT)等肝脏酶活性的影响。
JME对大鼠的半数致死量为3808mg/kg体重,而JEE的半数致死量大于5000mg/kg体重。给大鼠喂食这两种提取物后,一块肝脏组织的显微照片未显示明显的毒性症状。从相关研究来看,两种提取物都促使完整的线粒体打开其MMPT孔。与对照组相比,脂质过氧化物产物释放和ATP酶活性显著增加(P<0.05)。用JME处理时,在50mg/kg剂量下AST、ALT和GGT的活性均降低,但用JEE处理时AST的活性显著增强(P<0.05)。结果表明,Jatonik多草药混合物的JME和JEE均具有低毒性、显著的MMPT孔诱导作用以及增强的ATP酶活性,但MDA产生增加。
Jatonik提取物可能是凋亡失调疾病药物开发的一个有前景的靶点,然而,需要进一步研究以更好地阐明这些现象所涉及的分子机制。