Postexercise hypotension in conscious SHR is attenuated by blockade of substance P receptors in NTS

被引:26
作者
Chen, CY
Munch, PA
Quail, AW
Bonham, AC
机构
[1] Univ Calif Davis, Div Cardiovasc Med, Dept Internal Med, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Pharmacol, Davis, CA 95616 USA
[3] Univ Newcastle, Discipline Human Physiol, Newcastle, NSW 2308, Australia
[4] Univ Newcastle, Hunter Heart Lung Res Guild, Newcastle, NSW 2308, Australia
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2002年 / 283卷 / 05期
关键词
NK-1; receptor; exercise; microinjection; blood pressure; hypertension; nucleus tractus solitarius;
D O I
10.1152/ajpheart.00827.2001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In hypertensive subjects, a single bout of dynamic exercise results in an immediate lowering of blood pressure back toward normal. This postexercise hypotension (PEH) also occurs in the spontaneously hypertensive rat (SHR). In both humans and SHRs, PEH features a decrease in sympathetic nerve discharge, suggesting the involvement of central nervous system pathways. Given that substance P is released in the nucleus tractus solitarius (NTS) by activation of baroreceptor and skeletal muscle afferent fibers during muscle contraction, we hypothesized that substance P acting at neurokinin-1 (NK-1) receptors in the NTS might contribute to PEH. We tested the hypothesis by determining, in conscious SHRs, whether NTS microinjections of the NK-1 receptor antagonist SR-140333 before exercise attenuated PEH. The antagonist, in a dose (60 pmol) that blocked substance P- and spared D, L-homocysteic acid-induced depressor responses, significantly attenuated the PEH by 37%, whereas it had no effect on blood pressure during exercise. Vehicle microinjection had no effect. The antagonist also had no effect on heart rate responses during both exercise and the PEH period. The data suggest that a substance P (NK-1) receptor mechanism in the NTS contributes to PEH.
引用
收藏
页码:H1856 / H1862
页数:7
相关论文
共 57 条
[11]   IN-VITRO AND IN-VIVO BIOLOGICAL-ACTIVITIES OF SR140333, A NOVEL POTENT NONPEPTIDE TACHYKININ NK1, RECEPTOR ANTAGONIST [J].
EMONDSALT, X ;
DOUTREMEPUICH, JD ;
HEAULME, M ;
NELIAT, G ;
SANTUCCI, V ;
STEINBERG, R ;
VILAIN, P ;
BICHON, D ;
DUCOUX, JP ;
PROIETTO, V ;
VANBROECK, D ;
SOUBRIE, P ;
LEFUR, G ;
BRELIERE, JC .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 250 (03) :403-413
[12]   LABILE HYPERTENSION AND JOGGING - NEW DIAGNOSTIC-TOOL OR SPURIOUS DISCOVERY [J].
FITZGERALD, W .
BRITISH MEDICAL JOURNAL, 1981, 282 (6263) :542-544
[13]   POSTEXERCISE HYPOTENSION AND SYMPATHOINHIBITION IN BORDERLINE HYPERTENSIVE MEN [J].
FLORAS, JS ;
SINKEY, CA ;
AYLWARD, PE ;
SEALS, DR ;
THOREN, PN ;
MARK, AL .
HYPERTENSION, 1989, 14 (01) :28-35
[14]  
GATTI PJ, 1995, BRAIN RES, V181, P476
[15]   Substance P receptor-expressing neurons in the medullary and spinal dorsal horns projecting to the nucleus of the solitary tract in the rat [J].
Guan, ZL ;
Ding, YQ ;
Li, JL ;
Lü, BZ .
NEUROSCIENCE RESEARCH, 1998, 30 (03) :213-218
[16]  
Guyenet P. G., 1990, CENTRAL REGULATION A, P145
[17]   ROLE OF EXCITATORY AMINO-ACIDS IN RAT VAGAL AND SYMPATHETIC BAROREFLEXES [J].
GUYENET, PG ;
FILTZ, TM ;
DONALDSON, SR .
BRAIN RESEARCH, 1987, 407 (02) :272-284
[18]   Impaired sympathetic vascular regulation in humans after acute dynamic exercise [J].
Halliwill, JR ;
Taylor, JA ;
Eckberg, DL .
JOURNAL OF PHYSIOLOGY-LONDON, 1996, 495 (01) :279-288
[19]  
Hannum SM., 1981, Scand J Sports Sci, V3, P11
[20]  
HARA K, 1995, J HYPERTENS, V13, P447