Umbelliferone stimulates glucose uptake; modulates gluconeogenic and nucleotide-hydrolyzing enzymes activities, and dysregulated lipid metabolic pathways in isolated psoas muscle

被引:23
作者
Salau, Veronica F. [1 ,2 ]
Erukainure, Ochuko L. [1 ,4 ]
Ibeji, Collins U. [5 ]
Koorbanally, Neil A. [3 ]
Islam, Md Shahidul [1 ]
机构
[1] Univ KwaZulu Natal, Sch Life Sci, Dept Biochem, Westville Campus, ZA-4000 Durban, South Africa
[2] Veritas Univ, Dept Biochem, Abuja, Nigeria
[3] Univ KwaZulu Natal, Sch Chem & Phys, Westville Campus, ZA-4000 Durban, South Africa
[4] Univ Free State, Dept Pharmacol, ZA-9300 Bloemfontein, South Africa
[5] Univ Nigeria, Fac Phys Sci, Dept Pure & Ind Chem, Nsukka 410001, Nigeria
基金
新加坡国家研究基金会;
关键词
Glucose metabolism; Lipid metabolism; Muscle; Type; 2; diabetes; Umbelliferone; SKELETAL-MUSCLE; IN-VITRO; ALPHA-GLUCOSIDASE; INSULIN; ABSORPTION; EXTRACTS; HYPERGLYCEMIA; MECHANISM; THERAPY; FLOWER;
D O I
10.1016/j.jff.2020.103847
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The ability of umbelliferone to stimulate muscle glucose uptake and its effect on glucose and fatty acid metabolism as well as nucleotide hydrolysis and cholinergic activity were investigated in isolated psoas muscles. Incubation of umbelliferone with muscles led to increase glucose uptake, elevated GSH, SOD and catalase activities, as well as depleted malondialdehyde and nitric oxide levels. It also led to decrease ATPase activity with concomitant increase in ENTPDase and 5'nucleotidiase activities. The activities of chymotrypsin and acetylcholinesterase, glycogen phosphorylase, glucose-6-phosphatase, fructose-1,6-phosphatase and lipase were also suppressed. Umbelliferone reversed the altered lipid metabolites, and deactivated pathways induced by incubation with glucose. These were however reversed in umbelliferone-incubated muscles with concomitant deactivation of steroid biosynthesis. Taken together, these results further support the antidiabetic properties of umbelliferone. Its antidiabetic mechanism involves stimulation of muscle glucose uptake, with concomitant modulation of lipid metabolism and nucleotide hydrolysis, while stalling gluconeogenesis and oxidative stress.
引用
收藏
页数:15
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