EFFECT OF ATROPINE INJECTED INTO THE NUCLEUS-TRACTUS-SOLITARIUS ON THE REGULATION OF BLOOD-PRESSURE

被引:26
作者
TSUKAMOTO, K [1 ]
YIN, M [1 ]
SVED, AF [1 ]
机构
[1] UNIV PITTSBURGH,DEPT BEHAV NEUROSCI,PITTSBURGH,PA 15260
关键词
ACETYLCHOLINE; METHYLATROPINE; AORTIC DEPRESSOR NERVE; BAROREFLEX; MICROINJECTION;
D O I
10.1016/0006-8993(94)91898-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous experiments have demonstrated that stimulation of muscarinic cholinergic receptors in the nucleus tractus solitarius (NTS) of the rat decreases arterial blood pressure and heart rate. The present studies were designed to examine the role of cholinergic mechanisms in the NTS in the tonic regulation of arterial pressure and the baroreceptor reflex. Atropine injected into the NTS of chloralose-anesthetized rats produced a dose-dependent inhibition of cardiovascular responses elicited by injection of acetylcholine into the same site; 240 pmol atropine eliminated acetylcholine-evoked responses. Atropine also increased arterial brood pressure but only at higher doses. Even larger doses of atropine were required to alter cardiovascular responses elicited by electrical stimulation of the aortic depressor nerve. Methylatropine injected into the NTS also blocked acetylcholine-evoked responses but, in contrast to the actions of atropine, did not increase arterial pressure in the dose range required to block acetylcholine-evoked responses. Furthermore, a dose of methylatropine (1 nmol) capable of blocking acetylcholine-evoked cardiovascular responses did not alter aortic depressor nerve-evoked cardiovascular responses. This lack of an effect of methylatropine on arterial pressure and aortic depressor nerve-evoked responses was not due to limited diffusion of the drug within the NTS since 1 nmol methylatropine completely blocked acetylcholine-evoked responses even when injected 0.5 mm distant from the site of acetylcholine injection. These results suggest that cholinergic mechanisms in the NTS are not involved in the tonic regulation of cardiovascular function or the baroreceptor reflex. Furthermore, these results highlight the importance of characterizing doses of drugs used in microinjection studies.
引用
收藏
页码:9 / 15
页数:7
相关论文
共 26 条
[1]   ATROPINE LOWERS BLOOD-PRESSURE IN NORMOTENSIVE RATS THROUGH BLOCKADE OF ALPHA-ADRENERGIC RECEPTORS [J].
ABRAHAM, S ;
CANTOR, EH ;
SPECTOR, S .
LIFE SCIENCES, 1981, 28 (03) :315-322
[2]   LOCALIZATION OF CHOLINE-ACETYLTRANSFERASE IN PERIKARYA AND DENDRITES WITHIN THE NUCLEI OF THE SOLITARY TRACTS [J].
ARMSTRONG, DM ;
ROTLER, A ;
HERSH, LB ;
PICKEL, VM .
JOURNAL OF NEUROSCIENCE RESEARCH, 1988, 20 (03) :279-290
[3]   CHOLINERGIC MECHANISMS IN THE NUCLEUS TRACTUS SOLITARII AND CARDIOVASCULAR REGULATION IN THE RAT [J].
CRISCIONE, L ;
REIS, DJ ;
TALMAN, WT .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1983, 88 (01) :47-55
[4]   QUANTITATIVE DISTRIBUTION OF MUSCARINIC RECEPTORS AND CHOLINE-ACETYLTRANSFERASE IN RAT MEDULLA - EXAMINATION OF TRANSMITTER RECEPTOR MISMATCH [J].
ERNSBERGER, P ;
ARNERIC, SP ;
ARANGO, V ;
REIS, DJ .
BRAIN RESEARCH, 1988, 452 (1-2) :336-344
[5]  
Gilman A.G., 1980, PHARM BASIS THERAPEU
[6]   CHOLINE-ACETYLTRANSFERASE ACTIVITY IN THE NUCLEUS TRACTUS SOLITARIUS - REGULATION BY THE AFFERENT VAGUS NERVE [J].
HELKE, CJ ;
HANDELMANN, GE ;
JACOBOWITZ, DM .
BRAIN RESEARCH BULLETIN, 1983, 10 (04) :433-436
[7]   EFFECT OF VAGOTOMY ON CHOLINERGIC PARAMETERS IN NUCLEI OF RAT MEDULLA-OBLONGATA [J].
HOOVER, DB ;
HANCOCK, JC ;
DEPORTER, TE .
BRAIN RESEARCH BULLETIN, 1985, 15 (01) :5-11
[8]   CHOLINE-ACETYLTRANSFERASE CONTENT IN DISCRETE REGIONS OF RAT-BRAIN STEM [J].
KOBAYASHI, RM ;
BROWNSTEIN, M ;
SAAVEDRA, JM ;
PALKOVITS, M .
JOURNAL OF NEUROCHEMISTRY, 1975, 24 (04) :637-640
[9]   NEUROACTIVE SUBSTANCES IN THE DORSAL VAGAL COMPLEX OF THE MEDULLA-OBLONGATA - NUCLEUS OF THE TRACTUS SOLITARIUS, AREA POSTREMA, AND DORSAL MOTOR NUCLEUS OF THE VAGUS [J].
LESLIE, RA .
NEUROCHEMISTRY INTERNATIONAL, 1985, 7 (02) :191-211
[10]   DISTRIBUTION OF NEUROACTIVE SUBSTANCES IN THE DORSAL VAGAL COMPLEX OF THE MEDULLA-OBLONGATA [J].
PALKOVITS, M .
NEUROCHEMISTRY INTERNATIONAL, 1985, 7 (02) :213-219