Cold water swim stress increases the expression of neurotensin mRNA in the lateral hypothalamus and medial preoptic regions of the rat brain

被引:34
作者
Seta, KA
Jansen, HT
Kreitel, KD
Lehman, M
Behbehani, MM [1 ]
机构
[1] Univ Cincinnati, Dept Mol & Cellular Physiol, Cincinnati, OH 45221 USA
[2] Univ Cincinnati, Dept Anesthesia, Cincinnati, OH USA
[3] Univ Cincinnati, Ctr Reprod Biol, Dept Cell Biol, Cincinnati, OH USA
[4] Univ Cincinnati, Ctr Reprod Biol, Dept Neurobiol, Cincinnati, OH USA
[5] Univ Cincinnati, Ctr Reprod Biol, Dept VCAPP, Cincinnati, OH USA
[6] Washington State Univ, Dept Anat, Pullman, WA 99164 USA
来源
MOLECULAR BRAIN RESEARCH | 2001年 / 86卷 / 1-2期
关键词
neurotensin; cold water swim stress; medial preoptic area; lateral hypothalamus; in situ hybridization;
D O I
10.1016/S0169-328X(00)00279-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stress-induced analgesia is a well-documented phenomenon that occurs in all mammalian species. Forced cold water swim produces a type of stress-induced analgesia that is independent of mu opioid receptors. The neuropeptide neurotensin (NT) has been implicated in mu opioid-independent analgesia (MOIA), but the circuitry of this system is largely unknown. The medial preoptic area (MPO) and lateral hypothalamus (LH) are two regions that are known to modulate pain processing. These two regions also contain neurotensinergic projections to the periaqueductal gray, a region that has been shown to produce MOIA upon injection of NT. The goal of this study was to determine if cold water swim (CWS) stress, which produces MOIA, activates the NT-ergic systems in these two regions. In situ hybridization results indicate that CWS increases the level of NT mRNA within neurons in the MPO and LH, suggesting that these two regions are activated during this process. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:145 / 152
页数:8
相关论文
共 53 条
[1]  
AIMONE LD, 1988, J NEUROSCI, V8, P2652
[2]   SPINAL MONOAMINE MEDIATION OF STIMULATION-PRODUCED ANTINOCICEPTION FROM THE LATERAL HYPOTHALAMUS [J].
AIMONE, LD ;
GEBHART, GF .
BRAIN RESEARCH, 1987, 403 (02) :290-300
[3]  
ALAM MN, 1991, BRAIN RES, V566, P303
[4]   DISTRIBUTION OF NEUROTENSIN NEUROMEDIN-N MESSENGER-RNA IN RAT FOREBRAIN - UNEXPECTED ABUNDANCE IN HIPPOCAMPUS AND SUBICULUM [J].
ALEXANDER, MJ ;
MILLER, MA ;
DORSA, DM ;
BULLOCK, BP ;
MELLONI, RH ;
DOBNER, PR ;
LEEMAN, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) :5202-5206
[5]  
Baklavadzhyan O G, 1989, Neurosci Behav Physiol, V19, P42, DOI 10.1007/BF01148410
[6]   Properties of a projection pathway from the medial preoptic nucleus to the midbrain periaqueductal gray of the rat and its role in the regulation of cardiovascular function [J].
Behbehani, MM ;
Gomez, TMD .
BRAIN RESEARCH, 1996, 740 (1-2) :141-150
[7]  
BEHBEHANI MM, 1988, J NEUROSCI, V8, P2780
[8]   A MECHANISM FOR THE ANALGESIC EFFECT OF NEUROTENSIN AS REVEALED BY BEHAVIORAL AND ELECTROPHYSIOLOGICAL TECHNIQUES [J].
BEHBEHANI, MM ;
PERT, A .
BRAIN RESEARCH, 1984, 324 (01) :35-42
[9]   Low doses of neurotensin in the preoptic area produce hyperthermia. Comparison with other brain sites and with neurotensin-induced analgesia [J].
Benmoussa, M ;
Chait, A ;
Loric, G ;
deBeaurepaire, R .
BRAIN RESEARCH BULLETIN, 1996, 39 (05) :275-279
[10]   STRESS-PRODUCED ANALGESIA AND MORPHINE-PRODUCED ANALGESIA - LACK OF CROSS-TOLERANCE [J].
BODNAR, RJ ;
KELLY, DD ;
STEINER, SS ;
GLUSMAN, M .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1978, 8 (06) :661-666