Mechanistic study of attenuation of monosodium glutamate mixed high lipid diet induced systemic damage in rats by Coccinia grandis

• Published in: Scientific reports 2020-09, Vol.10 (1), p.15443, Article 15443
• Main Authors: Banerjee, Arnab, Das, Debasmita, Paul, Rajarshi, Roy, Sandipan, Das, Ujjal, Saha, Samrat, Dey, Sanjit, Adhikary, Arghya, Mukherjee, Sandip, Maji, Bithin Kumar
• Format: Article
• Language: English
• Subjects: 631/443; 692/700; Animals; Biomarkers - analysis; Cucurbitaceae - chemistry; Diet, High-Fat - adverse effects; Gene Expression Regulation; Humanities and Social Sciences; Hyperlipidemias - drug therapy; Hyperlipidemias - etiology; Hyperlipidemias - metabolism; Hyperlipidemias - pathology; Inflammation - drug therapy; Inflammation - etiology; Inflammation - metabolism; Inflammation - pathology; Male; Metabolic Syndrome - drug therapy; Metabolic Syndrome - etiology; Metabolic Syndrome - metabolism; Metabolic Syndrome - pathology; multidisciplinary; Oxidative Stress; Plant Extracts - pharmacology; Rats; Rats, Wistar; Science; Science (multidisciplinary); Sodium Glutamate - toxicity
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-72076-6

In the context of failure of treatment for non alcoholic fatty liver disease (NAFLD)-mediated systemic damages, recognition of novel and successful characteristic drug to combat these anomalous situations is earnestly required. The present study is aimed to evaluate protective value of ethanol extract of Coccinia grandis leaves (EECGL), naturally occurring medicinal plant, on NAFLD-mediated systemic damage induced by high lipid diet along with monosodium glutamate (HM)-fed rats. Our study uncovered that EECGL significantly ameliorates HM-induced hyperlipidemia, increased lipogenesis and metabolic disturbances (via up regulation of PPAR-α and PPAR-γ), oxidative stress (via reducing the generation of reactive oxygen species and regulating the redox-homeostasis) and inflammatory response (via regulating the pro-inflammatory and anti-inflammatory factors with concomitant down regulation of NF-kB, iNOS, TNF-α and up regulation of eNOS). Furthermore, EECGL significantly inhibited HM-induced increased population of cells in sub G0/G1 phase, decreased Bcl2 expression and thereby loss of mitochondrial membrane potential with over expression of Bax, p53, p21, activation of caspase 3 and 9 indicated the apoptosis and suppression of cell survival. It is perhaps the first comprehensive study with a mechanistic approach which provides a strong unique strategy for the management of HM-induced systemic damage with effective dose of EECGL.