Cargando…
Serum from Jiao-Tai-Wan treated rats increases glucose consumption by 3T3-L1 adipocytes through AMPK pathway signaling
Type 2 diabetes (T2DM) is characterized by hyperglycemia resulting from insulin resistance. Jiao-Tai-Wan (JTW), a traditional Chinese medicine consisting of a 10:1 formulation of Rhizoma Coptidis (RC) and Cortex Cinnamomi (cinnamon) was shown to have hypoglycemic efficacy in a type 2 diabetic mouse...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449522/ https://www.ncbi.nlm.nih.gov/pubmed/30886061 http://dx.doi.org/10.1042/BSR20181286 |
_version_ | 1783408865917796352 |
---|---|
author | Yuan, Lin Tang, Peng Li, Hui-Jiao Hu, Na Zhong, Xiao-Yu Lin, Min Sun, Yin-Qiang Lu, Min Lu, Xiong |
author_facet | Yuan, Lin Tang, Peng Li, Hui-Jiao Hu, Na Zhong, Xiao-Yu Lin, Min Sun, Yin-Qiang Lu, Min Lu, Xiong |
author_sort | Yuan, Lin |
collection | PubMed |
description | Type 2 diabetes (T2DM) is characterized by hyperglycemia resulting from insulin resistance. Jiao-Tai-Wan (JTW), a traditional Chinese medicine consisting of a 10:1 formulation of Rhizoma Coptidis (RC) and Cortex Cinnamomi (cinnamon) was shown to have hypoglycemic efficacy in a type 2 diabetic mouse model. Here we investigated whether glucose consumption by insulin-resistant adipocytes could be modulated by serum from JTW-treated rats, and if so, through what mechanism. JTW-medicated serum was prepared from rats following oral administration of JTW decoction twice a day for 4 days. Fully differentiated 3T3-L1 adipocytes – rendered insulin resistance by dexamethasone treatment – were cultured in medium containing JTW-medicated rat serum. JTW-medicated serum treatment increased glucose uptake, up-regulated levels of phosphorylated adenosine 5′-monophoshate-activated protein kinase (p-AMPK), and stimulated expression and translocation of glucose transporter 4 (GLUT4). JTW-medicated serum induced significantly greater up-regulation of p-AMPK and GLUT4 than either RC or cinnamon-medicated serum. JTW-medicated serum induced effects on 3T3-L1 adipocytes could be partially inhibited by treatment with the AMPK inhibitor compound C. In conclusion, JTW-medicated serum increased glucose consumption by IR adipocytes partially through the activation of the AMPK pathway, and JTW was more effective on glucose consumption than either RC or cinnamon alone. |
format | Online Article Text |
id | pubmed-6449522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64495222019-04-17 Serum from Jiao-Tai-Wan treated rats increases glucose consumption by 3T3-L1 adipocytes through AMPK pathway signaling Yuan, Lin Tang, Peng Li, Hui-Jiao Hu, Na Zhong, Xiao-Yu Lin, Min Sun, Yin-Qiang Lu, Min Lu, Xiong Biosci Rep Research Articles Type 2 diabetes (T2DM) is characterized by hyperglycemia resulting from insulin resistance. Jiao-Tai-Wan (JTW), a traditional Chinese medicine consisting of a 10:1 formulation of Rhizoma Coptidis (RC) and Cortex Cinnamomi (cinnamon) was shown to have hypoglycemic efficacy in a type 2 diabetic mouse model. Here we investigated whether glucose consumption by insulin-resistant adipocytes could be modulated by serum from JTW-treated rats, and if so, through what mechanism. JTW-medicated serum was prepared from rats following oral administration of JTW decoction twice a day for 4 days. Fully differentiated 3T3-L1 adipocytes – rendered insulin resistance by dexamethasone treatment – were cultured in medium containing JTW-medicated rat serum. JTW-medicated serum treatment increased glucose uptake, up-regulated levels of phosphorylated adenosine 5′-monophoshate-activated protein kinase (p-AMPK), and stimulated expression and translocation of glucose transporter 4 (GLUT4). JTW-medicated serum induced significantly greater up-regulation of p-AMPK and GLUT4 than either RC or cinnamon-medicated serum. JTW-medicated serum induced effects on 3T3-L1 adipocytes could be partially inhibited by treatment with the AMPK inhibitor compound C. In conclusion, JTW-medicated serum increased glucose consumption by IR adipocytes partially through the activation of the AMPK pathway, and JTW was more effective on glucose consumption than either RC or cinnamon alone. Portland Press Ltd. 2019-04-05 /pmc/articles/PMC6449522/ /pubmed/30886061 http://dx.doi.org/10.1042/BSR20181286 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Articles Yuan, Lin Tang, Peng Li, Hui-Jiao Hu, Na Zhong, Xiao-Yu Lin, Min Sun, Yin-Qiang Lu, Min Lu, Xiong Serum from Jiao-Tai-Wan treated rats increases glucose consumption by 3T3-L1 adipocytes through AMPK pathway signaling |
title | Serum from Jiao-Tai-Wan treated rats increases glucose consumption by 3T3-L1 adipocytes through AMPK pathway signaling |
title_full | Serum from Jiao-Tai-Wan treated rats increases glucose consumption by 3T3-L1 adipocytes through AMPK pathway signaling |
title_fullStr | Serum from Jiao-Tai-Wan treated rats increases glucose consumption by 3T3-L1 adipocytes through AMPK pathway signaling |
title_full_unstemmed | Serum from Jiao-Tai-Wan treated rats increases glucose consumption by 3T3-L1 adipocytes through AMPK pathway signaling |
title_short | Serum from Jiao-Tai-Wan treated rats increases glucose consumption by 3T3-L1 adipocytes through AMPK pathway signaling |
title_sort | serum from jiao-tai-wan treated rats increases glucose consumption by 3t3-l1 adipocytes through ampk pathway signaling |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449522/ https://www.ncbi.nlm.nih.gov/pubmed/30886061 http://dx.doi.org/10.1042/BSR20181286 |
work_keys_str_mv | AT yuanlin serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling AT tangpeng serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling AT lihuijiao serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling AT huna serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling AT zhongxiaoyu serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling AT linmin serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling AT sunyinqiang serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling AT lumin serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling AT luxiong serumfromjiaotaiwantreatedratsincreasesglucoseconsumptionby3t3l1adipocytesthroughampkpathwaysignaling |