Sahyadri Bio Labs Pvt. Ltd., Pannissery, Koonammoochy P.O, Thrissur - 680504, Kerala, India.
Sahyadri Bio Labs Pvt, Ltd., Pannissery, Koonammoochy P.O, Thrissur - 680504, Kerala, India; Department of Microbiology, Amala Cancer Research Centre, Amala Nagar, Thrissur-680 555, Kerala, India.
Int J Med Mushrooms. 2022;24(2):31-40. doi: 10.1615/IntJMedMushrooms.2022042125.
This study aimed to evaluate the effect of the polysaccharide-protein complex isolated from the fruiting bodies (GLFPPC) and cultured mycelia (GLMPPC) of a highly valued medicinal mushroom, Ganoderma lucidum, to alleviate doxorubicin (DOX)-induced cardiotoxicity. GLFPPC and GLMPPC were isolated from aqueous-alcoholic extracts of fruiting bodies and cultured mycelia of G. lucidum by repeated ethanol precipitation, dialysis, treatment with Sevag reagent, and freeze drying. The polysaccharide component was confirmed by assays with anthrone and phenol-sulphuric acid regents and protein moiety with Bradford reagent. The amino acid profile of protein moiety was determined by high-performance liquid chromatography analysis. DOX-induced cardiotoxicity was determined using Swiss albino mice. DOX administration caused a marked increase of creatine kinase and lactate dehydrogenase enzyme activities, indicating injury to the myocardium. The polysaccharide-protein complex downregulated cardiac injury marker enzymes, enhanced activities of endogenous antioxidants (namely, superoxide dismutase, catalase, glutathione peroxidase, and reduced glutathione levels), and significantly attenuated lipid peroxidation. The results indicated that GLFPPC and GLMPPC imparted protection against DOX-induced oxidative stress. Biochemical assays coupled with histopathological observations supported this conclusion. These experimental findings suggest that the polysaccharide-protein complex isolated from G. lucidum might be a useful therapeutic agent to ameliorate DOX-induced cardiomyopathy.
本研究旨在评估从珍贵药用蘑菇灵芝的子实体(GLFPPC)和培养菌丝体(GLMPPC)中分离得到的多糖-蛋白复合物对减轻阿霉素(DOX)诱导的心脏毒性的作用。GLFPPC 和 GLMPPC 是通过反复乙醇沉淀、透析、Sevag 试剂处理和冷冻干燥从灵芝子实体和培养菌丝体的水醇提取物中分离得到的。通过蒽酮和苯酚-硫酸试剂测定多糖成分,Bradford 试剂测定蛋白部分。采用高效液相色谱分析法测定蛋白部分的氨基酸组成。采用瑞士白化小鼠确定 DOX 诱导的心脏毒性。DOX 给药导致肌酸激酶和乳酸脱氢酶活性显著增加,表明心肌损伤。多糖-蛋白复合物下调心脏损伤标志物酶,增强内源性抗氧化剂(即超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶和还原型谷胱甘肽水平)的活性,并显著抑制脂质过氧化。结果表明,GLFPPC 和 GLMPPC 对 DOX 诱导的氧化应激具有保护作用。生化测定与组织病理学观察支持这一结论。这些实验结果表明,从灵芝中分离得到的多糖-蛋白复合物可能是一种有用的治疗药物,可改善 DOX 诱导的心肌病。