Oxidant stress-induced increase in myogenic activation of skeletal muscle resistance arteries in obese Zucker rats

被引:83
作者
Frisbee, JC
Maier, KG
Stepp, DW
机构
[1] Med Coll Wisconsin, Dept Physiol, Milwaukee, WI 53226 USA
[2] Med Coll Georgia, Dept Physiol, Vasc Biol Ctr, Augusta, GA 30912 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2002年 / 283卷 / 06期
关键词
skeletal muscle microcirculation; reactive oxygen species; regulation of vascular tone; Type II diabetes; hypertension; obesity;
D O I
10.1152/ajpheart.00379.2002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study characterized myogenic activation of skeletal muscle (gracilis) resistance arteries from lean (LZR) and obese Zucker rats (OZR). Arteries from OZR exhibited increased myogenic activation versus LZR; this increase was impaired by endothelium denudation or nitric oxde synthase inhibition. Treatment of vessels with 17-octadecynoic acid impaired responses in both strains by comparable amounts. Dihydroethidine microfluorography indicated elevated vascular superoxide levels in OZR versus LZR; immunohistochemistry demonstrated elevated vascular nitrotyrosine levels in OZR, indicating increased peroxynitrite presence. Vessel treatment with oxidative radical scavengers (polythylene glycol-superoxide dismutase/catalase) or inhibition of Ca2+-activated K+ (K-Ca) channels (iberiotoxin) did not alter myogenic activation in LZR but normalized activation in OZR. Application of peroxynitrite to vessels of OZR caused a greater vasoconstriction versus LZR; the response was impaired in OZR by elevated intraluminal pressure and was abolished in both strains by iberiotoxin. These results suggest that enhanced myogenic activation of gracilis arteries of OZR versus LZR 1) is not due to alterations in cytochrome P-450 contribution, and 2) may be due to elevated peroxynitrite levels inhibiting K-Ca channels following increased intraluminal pressure.
引用
收藏
页码:H2160 / H2168
页数:9
相关论文
共 36 条
[31]  
Vicaut E, 1999, DRUGS, V58, P1, DOI 10.2165/00003495-199958991-00001
[32]  
Wang MH, 1998, J PHARMACOL EXP THER, V284, P966
[33]  
Wolin Michael S., 1996, Microcirculation (Philadelphia), V3, P1, DOI 10.3109/10739689609146778
[34]  
Zimmermann PA, 1997, CIRC RES, V81, P996
[35]   20-HETE is an endogenous inhibitor of the large-conductance Ca2+-activated K+ channel in renal arterioles [J].
Zou, AP ;
Fleming, JT ;
Falck, JR ;
Jacobs, ER ;
Gebremedhin, D ;
Harder, DR ;
Roman, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1996, 270 (01) :R228-R237
[36]   INSULIN AND OBESITY IN ZUCKER GENETICALLY OBESE RAT FATTY [J].
ZUCKER, LM ;
ANTONIADES, HN .
ENDOCRINOLOGY, 1972, 90 (05) :1320-+