Effect and Mechanism of Ganoderma lucidum Spores on Alleviation of Diabetic Cardiomyopathy in a Pilot in vivo Study

• Published in: Diabetes, metabolic syndrome and obesity metabolic syndrome and obesity, 2020-01, Vol.13, p.4809-4822
• Main Authors: Shaher, Fahmi, Wang, Shuqiu, Qiu, Hongbin, Hu, Yu, Zhang, Yu, Wang, Weiqun, Al-Ward, Hisham, Abdulghani, Mahfoudh A M, Baldi, Salem, Zhou, Shaobo
• Format: Article
• Language: English
• Subjects: Analysis; Antibodies; Antioxidants; Apoptosis; Blood sugar; Cardiomyopathy; Diabetes; diabetic cardiomyopathy; Epilepsy; Experiments; Fluorides; ganoderma lucidum spore; Glucose; Glycogen; Heart diseases; Heart failure; Hemoglobin; Hyperglycemia; Inflammation; Kinases; Laboratory animals; Medical research; Medicine, Experimental; Muscle proteins; Natriuretic peptides; Original Research; Oxidative stress; pi3k/akt/mtor signaling pathway; Prevention; Proteins; Streptozocin
• ISSN: 1178-7007; 1178-7007
• DOI: 10.2147/DMSO.S281527

spores (GLS) exhibit disease prevention properties, but no study has been carried out on the anti-diabetic cardiomyopathy property of GLS. The aim of this study was to evaluate the hyperglycemia-mediated cardiomyopathy protection and mechanisms of GLS in streptozotocin (STZ)induced diabetic rats. Male SD rats were randomly divided into three groups. Two groups were given STZ (50 mg/kg, i.p.) treatment and when their fasting plasma glucose was above 16.7 mmol/L, among them, one group was given placebo, as diabetic group, and another group was given GLS (300 mg/kg) treatment. The group without STZ treatment was given placebo as a control group. The experiment lasted 70 days. The histology of myocardium and biomarkers of antioxidants, myocardial injury, pro-inflammatory cytokines, pro-apoptotic proteins and phosphorylation of key proteins in PI3K/AKT pathway were assessed. Biochemical analysis showed that GLS treatment significantly reduced the blood glucose (-20.3%) and triglyceride (-20.4%) levels compared to diabetic group without treatment. GLS treatment decreased the content of MDA (-25.6%) and activity of lactate dehydrogenase (-18.9%) but increased the activity of GSH-Px (65.4%). Western blot analysis showed that GLS treatment reduced the expression of both alpha-smooth muscle actin and brain natriuretic peptide. Histological analysis on the cardiac tissue micrographs showed that GLS treatment reduced collagen fibrosis and glycogen reactivity in myocardium. Both Western blot and immunohistochemistry analyses showed that GLS treatment decreased the expression levels of pro-inflammatory factors (cytokines IL-1β, and TNF-α) as well as apoptosis regulatory proteins (Bax, caspase-3 and -9), but increased Bcl-2. Moreover, GLS treatment significantly increased the phosphorylation of key proteins involved in PI3K/AKT pathway, eg, p-AKT p-PI3K and mTOR. The results indicated that GLS treatment alleviates diabetic cardiomyopathy by reducing hyperglycemia, oxidative stress, inflammation, apoptosis and further attenuating the fibrosis and myocardial dysfunction induced by STZ through stimulation of the PI3K/Akt/mTOR signaling pathway.