Intracellular lipid accumulation;
Hepatic steatosis;
Premna herbacea;
Dietary leafy vegetable of North East India;
Verbascoside;
Hepato-protection;
AMPK/SREBP/PPARa signaling pathways;
LIPID-ACCUMULATION;
LIVER;
AMPK;
GLUCOSE;
INFLAMMATION;
HOMEOSTASIS;
ACTIVATION;
PIP3;
D O I:
10.1016/j.fbio.2022.101720
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
Non-alcoholic fatty liver disease (NAFLD) includes a broad spectrum of liver dysfunction ranging from hepatic steatosis (intracellular triglyceride accumulation) to steatohepatitis. This study investigated the beneficial effect of Premna herbacea (a dietary leafy vegetable of North East India) and its active constituent in managing hepatic steatosis using high fat diet (HFD)-fed male Wistar rat and hepatocyte (CC1) cell culture models. Administration with methanolic leaf extract of Premna herbacea (PHME) (250 mg/kg body weight, oral gavage, 20 weeks) reduced the gain in body weight and rise in serum lipid (triglyceride and total cholesterol) levels and enzymes (alkaline phosphatase and aspartate aminotransferase) responsible for liver dysfunction in high fat diet (HFD)-fed rats. PHME administration further upregulated the phosphorylation of AMPK, ACC, and HMGCR, down-regulated SREBP1 signaling pathways of lipid metabolism, and prevented hepatic steatosis in liver tissues of HFD-fed rats. Moreover, studies on cultured hepatocytes revealed that treatment with both crude extract and its ethyl acetate fraction (PHEA) significantly reduced intracellular lipid accumulation in palmitate (PA, 0.75 mM)-treated cells. Chemical profiling (HPLC, HRMS, H-1 and C-13 NMR) of PHEA demonstrated the presence of Ver-bascoside, a caffeoyl phenylethanoid glycoside as a major phyto-constituent, which prevented cellular lipid accumulation and regulated the alteration in AMPK/SREBP/ACC/HMGCR signaling pathways of lipid meta-bolism in PA-treated cells. In conclusion, this study showed the prophylactic role of Premna herbacea and its active molecule, Verbascoside as a potential functional food in ameliorating hepatic steatosis by regulating AMPK/SREBP/ACC/HMGCR signaling cascade.
机构:
China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R ChinaChina Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
Zhang, Li
Li, Hui-Xia
论文数: 0引用数: 0
h-index: 0
机构:
China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R ChinaChina Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
Li, Hui-Xia
Pan, Wu-Si
论文数: 0引用数: 0
h-index: 0
机构:
China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R ChinaChina Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
Pan, Wu-Si
Khan, Farhan Ullah
论文数: 0引用数: 0
h-index: 0
机构:
Shanghai Jiao Tong Univ, Sch Pharm, 800 Dongchuan Rd, Shanghai 200240, Peoples R ChinaChina Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
Khan, Farhan Ullah
Qian, Cheng
论文数: 0引用数: 0
h-index: 0
机构:
Nanjing Med Univ, Sir Run Run Hosp, Dept Nephrol, Nanjing 211166, Jiangsu, Peoples R ChinaChina Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
Qian, Cheng
Qi-Li, Feng-Rong
论文数: 0引用数: 0
h-index: 0
机构:
China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R ChinaChina Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
Qi-Li, Feng-Rong
Xu, Xiaojun
论文数: 0引用数: 0
h-index: 0
机构:
China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
China Pharmaceut Univ, Jiangsu Key Lab Drug Discovery Metab Dis, Nanjing 210009, Jiangsu, Peoples R ChinaChina Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China