ETIOLOGY OF THE SEXUAL DIMORPHISM IN RENAL PERIPHERAL BENZODIAZEPINE RECEPTOR RESPONSE TO STRESS IN RATS

被引:14
作者
DRUGAN, RC
PARK, R
KAUFMAN, L
HOLMES, PV
机构
[1] Schrier Research Laboratory, Department of Psychology, Brown University, Providence
关键词
D O I
10.1006/hbeh.1993.1026
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
A sexual dimorphism in stress-induced alterations in renal peripheral benzodiazepine receptors (PBR) was recently reported. The present paper includes five experiments examining the etiology of this sex difference. Surgical removal of ovaries and testes was ineffective in altering the renal PBR stress response in both male and female rats. A diurnal variation in the sexual dimorphism was observed; the difference was seen in the early part of the light cycle, while the two sexes were indistinguishable at the end of the light cycle. Finally, based on recent data indicating the importance of the renin-angiotensin system in the stress-induced decrease in renal PBR, we examined both stress-induced plasma renin activity and renal PBR reactivity to exogenous angiotensin II (AII) administration in both sexes. Female rats show both an attenuated elevation of plasma renin levels in response to inescapable shock stress and a reduced PBR response to AII administration in comparison to males. The present data indicate that the renin-angiotensin system may be a critical factor in the sexual dimorphism in the renal PBE response to stress. The possibility of this difference in the renin-angiotensin system contributing to sex differences in susceptibility to escape deficits following inescapable shock is entertained. The implications for thee findings regarding the physiological function of the PBR are also discussed. © 1993 by Academic Press, Inc.
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页码:348 / 365
页数:18
相关论文
共 65 条
[1]   RESET OF FEEDBACK IN THE ADRENOCORTICAL SYSTEM - AN APPARENT SHIFT IN SENSITIVITY OF ADRENOCORTICOTROPIN TO INHIBITION BY CORTICOSTERONE BETWEEN MORNING AND EVENING [J].
AKANA, SF ;
CASCIO, CS ;
DU, JZ ;
LEVIN, N ;
DALLMAN, MF .
ENDOCRINOLOGY, 1986, 119 (05) :2325-2332
[2]   DEPLETION OF PERIPHERAL-TYPE BENZODIAZEPINE RECEPTORS AFTER HYPOPHYSECTOMY IN RAT ADRENAL-GLAND AND TESTIS [J].
ANHOLT, RRH ;
DESOUZA, EB ;
KUHAR, MJ ;
SNYDER, SH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1985, 110 (01) :41-46
[3]   TISSUE SPECIFIC REGULATION OF PERIPHERAL-TYPE BENZODIAZEPINE RECEPTOR DENSITY AFTER CHEMICAL SYMPATHECTOMY [J].
BASILE, AS ;
SKOLNICK, P .
LIFE SCIENCES, 1988, 42 (03) :273-283
[4]  
BASILE AS, 1987, J PHARMACOL EXP THER, V240, P1006
[5]   MAXIMAL ELECTROSHOCK INCREASES THE DENSITY OF [H-3] RO 5-4864 BINDING TO MOUSE CEREBRAL-CORTEX [J].
BASILE, AS ;
WEISSMAN, BA ;
SKOLNICK, P .
BRAIN RESEARCH BULLETIN, 1987, 19 (01) :1-7
[6]   ADRENALECTOMY REDUCES THE DENSITY OF PERIPHERAL-TYPE BINDING-SITES FOR BENZODIAZEPINES IN THE RAT-KIDNEY [J].
BASILE, AS ;
PAUL, SM ;
SKOLNICK, P .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1985, 110 (01) :149-150
[7]   HORMONAL DETERMINANTS OF SEX DIFFERENCES IN AVOIDANCE BEHAVIOR AND REACTIVITY TO ELECTRIC SHOCK IN RAT [J].
BEATTY, WW ;
BEATTY, PA .
JOURNAL OF COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1970, 73 (03) :446-&
[8]  
BENAVIDES J, 1983, ARCH INT PHARMACOD T, V266, P38
[9]   LABELING OF PERIPHERAL-TYPE BENZODIAZEPINE BINDING-SITES IN THE RAT-BRAIN BY USING [PK-H-3 11195, AN ISOQUINOLINE CARBOXAMIDE DERIVATIVE - KINETIC-STUDIES AND AUTORADIOGRAPHIC LOCALIZATION [J].
BENAVIDES, J ;
QUARTERONET, D ;
IMBAULT, F ;
MALGOURIS, C ;
UZAN, A ;
RENAULT, C ;
DUBROEUCQ, MC ;
GUEREMY, C ;
LEFUR, G .
JOURNAL OF NEUROCHEMISTRY, 1983, 41 (06) :1744-1750
[10]   DIFFERENTIAL REGULATION OF CENTRAL AND PERIPHERAL BENZODIAZEPINE BINDING-SITES IN THE RAT OLFACTORY-BULB [J].
BOLGER, GT ;
MEZEY, E ;
COTT, J ;
WEISSMAN, BA ;
PAUL, SM ;
SKOLNICK, P .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1984, 105 (1-2) :143-148