Abscisic acid enriched fig extract promotes insulin sensitivity by decreasing systemic inflammation and activating LANCL2 in skeletal muscle

被引:21
作者
Leber, Andrew [1 ,2 ]
Hontecillas, Raquel [1 ,2 ]
Tubau-Juni, Nuria [1 ,2 ]
Zoccoli-Rodriguez, Victoria [1 ,2 ]
Goodpaster, Bret [3 ]
Bassaganya-Riera, Josep [1 ,2 ]
机构
[1] NIMML Inst, Blacksburg, VA 24060 USA
[2] BioTherapeutics, Blacksburg, VA 24060 USA
[3] AdventHlth Res Inst, Orlando, FL 32804 USA
基金
美国国家卫生研究院;
关键词
TYPE-2; DIABETES-MELLITUS; GLUCOSE-TOLERANCE; PROTEIN-2; LANCL2; FATTY-ACIDS; RESISTANCE; CELLS; ACCUMULATION; ADIPOCYTES; MACROPHAGE; EXPRESSION;
D O I
10.1038/s41598-020-67300-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Abscisic acid is a phytohormone found in fruits and vegetables and is endogenously produced in mammals. In humans and mice, lanthionine synthetase C-like 2 (LANCL2) has been characterized as the natural receptor for ABA. Herein, we characterize the efficacy of a fig fruit extract of ABA in promoting glycemic control. This ABA-enriched extract, at 0.125 mu g ABA/kg body weight, improves glucose tolerance, insulin sensitivity and fasting blood glucose in diet-induced obesity (DIO) and db/db mouse models. In addition to decreasing systemic inflammation and providing glycemic control without increasing insulin, ABA extract modulates the metabolic activity of muscle. ABA increases expression of important glycogen synthase, glucose, fatty acid and mitochondrial metabolism genes and increases direct measures of fatty acid oxidation, glucose oxidation and metabolic flexibility in soleus muscle cells from ABA-treated mice with DIO. Glycolytic and mitochondrial ATP production were increased in ABA-treated human myotubes. Further, ABA synergized with insulin to dramatically increase the rate of glycogen synthesis. The loss of LANCL2 in skeletal muscle abrogated the effect of ABA extract in the DIO model and increased fasting blood glucose levels. This data further supports the clinical development of ABA in the treatment of pre-diabetes, type 2 diabetes and metabolic syndrome.
引用
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页数:9
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