(-)-Epicatechin is associated with increased angiogenic and mitochondrial signalling in the hindlimb of rats selectively bred for innate low running capacity

被引:34
|
作者
Huettemann, Maik [1 ,2 ]
Lee, Icksoo [1 ]
Perkins, Guy A. [3 ]
Britton, Steven L. [4 ]
Koch, Lauren G. [4 ]
Malek, Moh H. [2 ,5 ]
机构
[1] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Cardiovasc Res Inst, Detroit, MI 48201 USA
[3] Univ Calif San Diego, Natl Ctr Microscopy & Imaging Res, La Jolla, CA 92093 USA
[4] Univ Michigan, Dept Anesthesiol, Ann Arbor, MI 49109 USA
[5] Wayne State Univ, Eugene Applebaum Coll Pharm & Hlth Sci, Integrat Physiol Exercise Lab, Detroit, MI 48201 USA
基金
美国国家卫生研究院;
关键词
dark chocolate; epicatechin; natural compound; nutrition; supplementation; CYTOCHROME-C-OXIDASE; SKELETAL-MUSCLE ANGIOGENESIS; LOW AEROBIC CAPACITY; ENDOTHELIAL GROWTH-FACTOR; FIBER-TYPE; ARTIFICIAL SELECTION; OXIDATIVE-PHOSPHORYLATION; ANATOMIC CAPILLARIZATION; COACTIVATOR PGC-1-BETA; INSULIN SENSITIVITY;
D O I
10.1042/CS20120469
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Alternative approaches to reduce congenital muscle dysfunction are needed in cases where the ability to exercise is limited. (-)-Epicatechin is found in cocoa and may stimulate capillarity and mitochondrial proliferation in skeletal muscle. A total of 21 male rats bred for LCR (low running capacity) from generation 28 were randomized into three groups: vehicle for 30 days (control); (-)-epicatechin for 30 days; and (-)-epicatechin for 30 days followed by 15 days without (-)-epicatechin. Groups 2 and 3 received 1.0 mg of (-)-epicatechin/kg of body mass twice daily, whereas water was given to the control group. The plantaris muscle was harvested for protein and morphometric analyses. In addition, in vitro experiments were conducted to examine the role of (-)-epicatechin on mitochondrial respiratory kinetics at different incubation periods. Treatment for 30 days with (-)-epicatechin increased capillarity (P<0.001) and was associated with increases in protein expression of VEGF (vascular endothelial growth factor)-A with a concomitant decrease in TSP-1 (thrombospondin-1) and its receptor, which remained after 15 days of (-)-epicatechin cessation. Analyses of the p38 MAPK (mitogen-activated protein kinase) signalling pathway indicated an associated increase in phosphorylation of MKK3/6 (MAPK kinase 3/6) and p38 and increased protein expression of MEF2A (myocyte enhancer factor 2A). In addition, we observed significant increases in protein expression of PGC-1 alpha (peroxisome-proliferator-activated receptor gamma co-activator 1 alpha), PGC-1 beta, Tfann and cristae abundance. Interestingly, these increases associated with (-)-epicatechin treatment remained after 15 days of cessation. Lastly, in vitro experiments indicated that acute exposure of LCR muscle to (-)-epicatechin incubation was not sufficient to increase mitochondrial respiration. The results suggest that increases in skeletal muscle capillarity and mitochondrial biogenesis are associated with 30 days of (-)-epicatechin treatment and sustained for 15 days following cessation of treatment. Clinically, the use of this natural compound may have potential application in populations that experience muscle fatigue and are unable to perform endurance exercise.
引用
收藏
页码:663 / 674
页数:12
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