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Effects of Microbial Metabolites of (-)-Epigallocatechin Gallate on Glucose Uptake in L6 Skeletal Muscle Cell and Glucose Tolerance in ICR Mice.
- Source :
-
Biological & pharmaceutical bulletin [Biol Pharm Bull] 2019; Vol. 42 (2), pp. 212-221. - Publication Year :
- 2019
-
Abstract
- Glucose uptake ability into L6 skeletal muscle cell was examined with eleven kinds of ring fission metabolites of (-)-epigallocatechin gallate (EGCG) produced by intestinal bacteria. The metabolites 5-(3,5-dihydroxyphenyl)-γ-valerolactone (EGC-M5), 4-hydroxy-5-(3,4,5-trihydroxyphenyl)valeric acid (EGC-M6), 5-(3,4,5-trihydroxyphenyl)-γ-valerolactone (EGC-M7) and 5-(3-hydroxyphenyl)valeric acid (EGC-M11) have been found to promote uptake of glucose into L6 myotubes significantly. EGC-M5, which is one of the major ring fission metabolites of EGCG, was also found to have a promotive effect on glucose transporter 4 (GLUT4) translocation accompanied by phosphorylation of AMP-activated protein kinase (AMPK) signaling pathway in skeletal muscle both in vivo and in vitro. Furthermore, the effect of oral single dosage of EGC-M5 on glucose tolerance test with ICR mice was examined and significant suppression of hyperglycemia was observed. These data suggested that EGC-M5 has an antidiabetic effect in vivo.
- Subjects :
- AMP-Activated Protein Kinases metabolism
Animals
Blood Glucose metabolism
Catechin chemistry
Catechin metabolism
Catechin pharmacology
Cell Line
Gastrointestinal Microbiome
Glucose Tolerance Test
Hypoglycemic Agents
Lactones metabolism
Lactones pharmacology
Male
Mice
Mice, Inbred ICR
Phosphorylation
Signal Transduction drug effects
Catechin analogs & derivatives
Glucose metabolism
Muscle Fibers, Skeletal drug effects
Muscle Fibers, Skeletal metabolism
Myoblasts, Skeletal drug effects
Myoblasts, Skeletal metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1347-5215
- Volume :
- 42
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Biological & pharmaceutical bulletin
- Publication Type :
- Academic Journal
- Accession number :
- 30713253
- Full Text :
- https://doi.org/10.1248/bpb.b18-00612