Therapeutic Potential of Diosgenin in Amelioration of Carbon Tetrachloride-Induced Murine Liver Injury.

IF 1.7 Q3 PHARMACOLOGY & PHARMACY
Drug Research Pub Date : 2024-04-01 Epub Date: 2024-03-08 DOI:10.1055/a-2263-1329
Mohamad-Hasan Ghosian-Moghaddam, Parvaneh Mohseni-Moghaddam, Mehrdad Roghani
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引用次数: 0

Abstract

Diosgenin is a sapogenin with antidiabetic, antioxidant, and anti-inflammatory properties. The current study investigated whether diosgenin could ameliorate carbon tetrachloride (CCL4)-induced liver injury. To cause liver injury, CCL4 was injected intraperitoneally twice a week for 8 weeks. Daily oral administration of diosgenin at doses of 20, 40, and 80 mg/kg was started one day before CCL4 injection and continued for 8 weeks. Finally, serum levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and also albumin were assessed. Catalase and superoxide dismutase (SOD) activities in addition to glutathione (GSH) and malondialdehyde (MDA) levels were also quantified in the liver homogenate and routine histological evaluation was also conducted. Elevated serum levels of liver enzymes and decreased serum level of albumin caused by CCL4 were significantly restored following diosgenin administration at doses of 40 and 80 mg/kg. Long-term administration of CCL4 increased inflammatory and apoptotic factors such as IL-1β, caspase 3, TNF-α, and IL-6 and decreased SOD and catalase activities as well as GSH level in liver homogenates; while MDA level was increased. Treatment with diosgenin increased SOD and catalase activities and GSH levels in the liver of injured animals. In addition, liver MDA, IL-1β, caspase 3, TNF-α, and IL-6 level or activity decreased by diosgenin treatment. Additionally, diosgenin aptly prevented aberrant liver histological changes. According to obtained results, diosgenin can dose-dependently diminish CCl4-induced liver functional deficits and histological changes in a dose-dependent manner, possibly due to its antioxidant and anti-inflammation properties, and its beneficial effect is comparable to known hepatoprotective agent silymarin.

薯蓣皂苷在改善四氯化碳诱发的小鼠肝损伤中的治疗潜力
薯蓣皂苷是一种具有抗糖尿病、抗氧化和抗炎特性的苷元。本研究探讨了薯蓣皂苷能不能改善四氯化碳(CCL4)诱导的肝损伤。为了造成肝损伤,每周两次腹腔注射 CCL4,连续注射 8 周。在注射 CCL4 前一天开始每天口服剂量为 20、40 和 80 毫克/千克的薯蓣皂苷,并持续 8 周。最后,对血清中的天门冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)和白蛋白水平进行了评估。此外,还对肝脏匀浆中的过氧化氢酶和超氧化物歧化酶(SOD)活性、谷胱甘肽(GSH)和丙二醛(MDA)水平进行了量化,并进行了常规组织学评估。在服用剂量为 40 和 80 毫克/千克的 diosgenin 后,CCL4 导致的肝酶血清水平升高和白蛋白血清水平降低得到了显著恢复。长期服用 CCL4 会增加炎症和凋亡因子,如 IL-1β、caspase 3、TNF-α 和 IL-6,降低 SOD 和过氧化氢酶活性以及肝匀浆中的 GSH 水平,同时增加 MDA 水平。使用薯蓣皂苷治疗可提高损伤动物肝脏中的 SOD 和过氧化氢酶活性以及 GSH 水平。此外,肝脏中的 MDA、IL-1β、caspase 3、TNF-α 和 IL-6 的水平或活性也在 diosgenin 处理后下降。此外,薯蓣皂苷能有效防止肝脏组织学的异常变化。研究结果表明,薯蓣皂苷能以剂量依赖的方式减轻CCl4诱导的肝功能缺陷和组织学变化,这可能是由于薯蓣皂苷的抗氧化和抗炎特性,其有益效果与已知的保肝药物水飞蓟素相当。
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来源期刊
Drug Research
Drug Research PHARMACOLOGY & PHARMACY-
CiteScore
3.50
自引率
0.00%
发文量
67
期刊介绍: Drug Research (formerly Arzneimittelforschung) is an international peer-reviewed journal with expedited processing times presenting the very latest research results related to novel and established drug molecules and the evaluation of new drug development. A key focus of the publication is translational medicine and the application of biological discoveries in the development of drugs for use in the clinical environment. Articles and experimental data from across the field of drug research address not only the issue of drug discovery, but also the mathematical and statistical methods for evaluating results from industrial investigations and clinical trials. Publishing twelve times a year, Drug Research includes original research articles as well as reviews, commentaries and short communications in the following areas: analytics applied to clinical trials chemistry and biochemistry clinical and experimental pharmacology drug interactions efficacy testing pharmacodynamics pharmacokinetics teratology toxicology.
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