Stress increases oxytocin release within the hypothalamic paraventricular nucleus

被引:150
作者
Nishioka, T
Anselmo-Franci, JA
Li, P
Callahan, MF
Morris, M
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27157 USA
[2] Univ Sao Paulo, Fac Odontol Ribeirao Preto, Sao Paulo, Brazil
关键词
microdialysis; oxytocin; vasopressin; stress; hypothalamus;
D O I
10.1016/S0006-8993(97)01159-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Evidence indicates that the hypothalamic paraventricular nucleus (PVN) and oxytocin (OT) neurons in particular play a role in the physiological response to stress. Microdialysis (MD) experiments were performed to determine whether OT is released into the PVN during shaker stress. Male rats were prepared with venous catheters and PVN guide cannulae, OT and vasopressin (VP) release into PVN and peripheral blood were measured under basal conditions and during and after shaker stress (10 min at 110 cycles/min). Stress produced a specific increase in PVN and plasma OT. Dialysate OT levels were 0.3 +/- 0.1, 2.8 +/- 1.2 and 1.3 +/- 0.6 pg/sample (control, stress and recovery, respectively). Plasma OT was significantly increased during stress (3.7 +/- 1.2 vs. 11.7 +/- 2.3 pg/ml, basal vs. stress, respectively). When MD probes were located outside the PVN, there was no increase in OT release, demonstrating site specificity. Stress produced no change in VP levels, either in dialysate or plasma. These results show that OT, but not VP, is released into the PVN and peripheral blood in response to shaker stress. The data raise the possibility that local release of OT into the PVN plays a role in the neuroendocrine stress cascade. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:57 / 61
页数:5
相关论文
共 35 条
[1]   CENTRAL OXYTOCIN SYSTEMS MAY MEDIATE A CARDIOVASCULAR-RESPONSE TO ACUTE STRESS IN RATS [J].
CALLAHAN, MF ;
KIRBY, RF ;
CUNNINGHAM, JT ;
ESKRIDGESLOOP, SL ;
JOHNSON, AK ;
MCCARTY, R ;
GRUBER, KA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (05) :H1369-H1377
[2]   EXCITOTOXIN PARAVENTRICULAR NUCLEUS LESIONS - STRESS AND ENDOCRINE REACTIVITY AND OXYTOCIN MESSENGER-RNA LEVELS [J].
CALLAHAN, MF ;
THORE, CR ;
SUNDBERG, DK ;
GRUBER, KA ;
OSTEEN, K ;
MORRIS, M .
BRAIN RESEARCH, 1992, 597 (01) :8-15
[3]   The role of oxytocin release in the paraventricular nucleus in the control of maternal behaviour in the sheep [J].
DaCosta, APC ;
GuevaraGuzman, RG ;
Ohkura, S ;
Goode, JA ;
Kendrick, KM .
JOURNAL OF NEUROENDOCRINOLOGY, 1996, 8 (03) :163-177
[6]   EFFECTS OF OXYTOCIN ON EMOTIONAL-STRESS AND STRESS-INDUCED GASTRIC-LESIONS [J].
GRASSI, M ;
DRAGO, F .
JOURNAL OF PHYSIOLOGY-PARIS, 1993, 87 (04) :261-264
[7]   Compression of the pituitary stalk elicits chronic increases in CSF vasopressin, oxytocin as well as in social investigation and aggressiveness [J].
Haller, J ;
Makara, GB ;
Barna, I ;
Kovacs, K ;
Nagy, J ;
Vecsernyes, M .
JOURNAL OF NEUROENDOCRINOLOGY, 1996, 8 (05) :361-365
[8]  
HASHIGUCHI H, 1997, BRAIN BEHAV, V61, P731
[9]   CENTRAL AND SYSTEMIC OXYTOCIN RELEASE - A STUDY OF THE PARAVENTRICULAR NUCLEUS BY INVIVO MICRODIALYSIS [J].
HATTORI, T ;
SUNDBERG, DK ;
MORRIS, M .
BRAIN RESEARCH BULLETIN, 1992, 28 (02) :257-263
[10]   ASSESSMENT OF THE RELATIVE CONTRIBUTION OF PERIPHERAL AND CENTRAL COMPONENTS IN COCAINE PLACE CONDITIONING [J].
HEMBY, SE ;
JONES, GH ;
HUBERT, GW ;
NEILL, DB ;
JUSTICE, JB .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1994, 47 (04) :973-979