Laminarin counteracts diet-induced obesity associated with glucagon-like peptide-1 secretion.
Laminarin counteracts diet-induced obesity associated with glucagon-like peptide-1 secretion.
复制标题
海带多糖可抵消与胰高血糖素样肽-1 分泌相关的饮食引起的肥胖
DOI:
10.18632/oncotarget.19957
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发表时间:
2017-11-21
期刊:
影响因子:
--
通讯作者:
Shu G
中科院分区:
文献类型:
--
作者:
Yang L;Wang L;Zhu C;Wu J;Yuan Y;Yu L;Xu Y;Xu J;Wang T;Liao Z;Wang S;Zhu X;Gao P;Zhang Y;Wang X;Jiang Q;Shu G
Laminarin, a type of β-glucan isolated from brown seaweeds, exhibits verity of physiological activities, which include immunology modulation and antitumor function. To investigate the effect of laminarin on energy homeostasis, mice were orally administrated with laminarin to test food intake, fat deposition, and glucose homeostasis. Chronically, laminarin treatment significantly decreases high-fat-diet-induced body weight gain and fat deposition and reduces blood glucose level and glucose tolerance. Acutely, laminarin enhances serum glucagon-like peptide-1 (GLP-1) content and the mRNA expression level of proglucagon and prohormone convertase 1 in ileum. Subsequently, laminarin suppresses the food intake of mice, the hypothalamic AgRP neuron activity, and AgRP expression but activates pancreatic function. Furthermore, laminarin-induced appetite reduction was totally blocked by Exendin (9-39), a specific competitive inhibitor of GLP-1 receptor. Then, STC-1 cells were adopted to address the underlying mechanism, by which laminarin promoted GLP-1 secretion in vitro. Results showed that laminarin dose-dependently promoted GLP-1 secretion and c-Fos protein expression in STC-1 cells, which were independent of Dectin-1 and CD18. Interestingly, BAPTA-AM, a calcium-chelating agent, potently attenuated laminarin-induced [Ca2+]i elevation, c-Fos expression, and GLP-1 secretion. In summary, our data support that laminarin counteracts diet-induced obesity and stimulates GLP-1 secretion via [Ca2+]i; this finding provides an experimental basis for laminarin application to treat obesity and maintain glucose homeostasis.
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影响因子:
--
作者:
Dharmalingam M;Sriram U;Baruah MP
通讯作者:
Baruah MP
影响因子:
7.7
作者:
Arakawa M;Mita T;Azuma K;Ebato C;Goto H;Nomiyama T;Fujitani Y;Hirose T;Kawamori R;Watada H
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Watada H
影响因子:
7.7
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通讯作者:
Reimann, F
影响因子:
56.9
作者:
Chawla, S;Hardingham, GE;Bading, H
通讯作者:
Bading, H
影响因子:
2.2
作者:
Fuentes, Ana-Lucia;Millis, Leonard;Sigola, Lynette
通讯作者:
Sigola, Lynette