Khalili Azadeh, Fallah Parviz, Hashemi Seyed Ali, Ahmadian-Attari Mohammad Mahdi, Jamshidi Vahid, Mazloom Roham, Beikzadeh Leila, Bayat Gholamreza
Department of Physiology-Pharmacology-Medical Physic, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran.
Evidence-based Phytotherapy and Complementary Medicine Research Center, Alborz University of Medical Sciences, Karaj, Iran.
Avicenna J Phytomed. 2021 Jul-Aug;11(4):367-379. doi: 10.22038/AJP.2020.17281.
Farnesoid-X-activated receptors (FXR) are key modulators of liver regeneration. Milk thistle and Chicory are known as potent protective remedies in several liver disorders. The objective of this work was to examine the role of in the hepato-healing properties of milk thistle (MTE) and chicory extracts (CE) in a rat model of acetaminophen-induced hepatotoxicity.
Male Wistar rats were randomly divided into seven groups including control, vehicle, acetaminophen (500 mg/kg/day, oral), acetaminophen plus oral MTE 200 and 400 mg/kg/day, and acetaminophen plus oral CE 500 and 1000 /kg/day for 28 days. Liver function and histology as well as the pattern of hepatic expression were assessed after 4 weeks.
Administration of acetaminophen was associated with a significant elevation of liver transaminase along with the architectural injuries. In contrast, chronic concomitant administration of both MTE and CE significantly restored the liver function and structural abnormality. The main molecular findings of the study revealed that the lower doses of both MTE and CE led to a marked upregulation of hepatic expression.
Discovery of the involvement of the nuclear modulating pathways in hepatoprotective activity of the extracts, providesa new mechanistic insight which needs further investigations.
法尼酯X激活受体(FXR)是肝脏再生的关键调节因子。水飞蓟和菊苣在多种肝脏疾病中被认为是有效的保护性药物。本研究的目的是在对乙酰氨基酚诱导的肝毒性大鼠模型中,研究[此处原文缺失内容]在水飞蓟提取物(MTE)和菊苣提取物(CE)肝脏修复特性中的作用。
雄性Wistar大鼠随机分为七组,包括对照组、赋形剂组、对乙酰氨基酚组(500毫克/千克/天,口服)、对乙酰氨基酚加口服MTE 200和400毫克/千克/天组,以及对乙酰氨基酚加口服CE 500和1000毫克/千克/天组,持续给药28天。4周后评估肝功能、组织学以及肝脏[此处原文缺失内容]表达模式。
给予对乙酰氨基酚会导致肝转氨酶显著升高以及结构损伤。相比之下,MTE和CE的长期联合给药显著恢复了肝功能和结构异常。该研究的主要分子学发现表明,较低剂量的MTE和CE均导致肝脏[此处原文缺失内容]表达显著上调。
发现核调节途径参与提取物的肝脏保护活性,提供了一个新的机制性见解,这需要进一步研究。