Chronic immobilization stress reduces sodium intake and renal excretion in rats

被引:10
作者
Bensi, N
Bertuzzi, M
Armario, A
Gauna, HF
机构
[1] UNIV NACL RIO CUARTO,DEPT MOL BIOL,RA-5800 RIO CUARTO,CORDOBA,ARGENTINA
[2] UNIV AUTONOMA BARCELONA,FAC CIENCIAS,DEPT BIOL CELULAR & FISIOL,UNIDAD FISIOL ANIM,E-08193 BARCELONA,SPAIN
关键词
sodium intake; natriuresis; kaliuresis; diuresis; immobilization stress; adaptation;
D O I
10.1016/S0031-9384(97)00197-2
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
The influence of chronic exposure to immobilization (IMO) on sodium appetite as well as sodium and potassium renal excretion in adult male Wistar rats was studied. The animals were individually housed and all variables under observation were measured in metabolic cages the first, seventh, and thirteenth days once the experiment had started. Half of the rats had access to water, and the remainder of the rats had access to both water and saline solution (1.5% NaCl). IMO reduced the intake of saline solution. Renal water, sodium, and potassium excretion in those IMO rats having access to saline were lower than in control rats. The effects of IMO were very similar during all observation days; therefore no evidence of adaptation to repented stress was found. The present data indicate the following: (i) IMO stress reduced sodium appetite, probably as a secondary effect to the deficit in sodium renal excretion; (ii) IMO caused antidiuresis and antikaliuresis, only in those rats taking saline solution; (iii) no adaptation to repeated IMO stress was found in any of the tested variables. The reduction of sodium appetite observed in stressed rats might be a homeostatic mechanism to maintain sodium balance after impairment of renal sodium excretion caused by stress. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:1391 / 1396
页数:6
相关论文
共 29 条
[1]   PROGRESSIVE HYPERTENSION IN DOGS BY AVOIDANCE-CONDITIONING AND SALINE INFUSION [J].
ANDERSON, DE ;
KEARNS, WD ;
BETTER, WE .
HYPERTENSION, 1983, 5 (03) :286-291
[2]   EVIDENCE THAT THE PITUITARY-ADRENAL AXIS DOES NOT CROSS-ADAPT TO STRESSORS - COMPARISON TO OTHER PHYSIOLOGICAL VARIABLES [J].
ARMARIO, A ;
HIDALGO, J ;
GIRALT, M .
NEUROENDOCRINOLOGY, 1988, 47 (03) :263-267
[3]   RESPONSE OF ANTERIOR-PITUITARY HORMONES TO CHRONIC STRESS - THE SPECIFICITY OF ADAPTATION [J].
ARMARIO, A ;
LOPEZCALDERON, A ;
JOLIN, T ;
BALASCH, J .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1986, 10 (03) :245-250
[4]   CARDIOVASCULAR AND SYMPATHOADRENAL RESPONSES TO STRESS IN SWIM-TRAINED RATS [J].
COX, RH ;
HUBBARD, JW ;
LAWLER, JE ;
SANDERS, BJ ;
MITCHELL, VP .
JOURNAL OF APPLIED PHYSIOLOGY, 1985, 58 (04) :1207-1214
[5]   EXERCISE TRAINING ATTENUATES STRESS-INDUCED HYPERTENSION IN THE RAT [J].
COX, RH ;
HUBBARD, JW ;
LAWLER, JE ;
SANDERS, BJ ;
MITCHELL, VP .
HYPERTENSION, 1985, 7 (05) :747-751
[6]   GENETIC PREDISPOSITION AND STRESS-INDUCED HYPERTENSION [J].
FRIEDMAN, R ;
IWAI, J .
SCIENCE, 1976, 193 (4248) :161-162
[7]   EFFECT OF CHRONIC STRESS IN THE BLOOD-PRESSURE IN THE RAT - ACTH ADMINISTRATION [J].
GAMALLO, A ;
ALARIO, P ;
VILLANUA, MA ;
NAVA, MP .
HORMONE AND METABOLIC RESEARCH, 1988, 20 (06) :336-338
[9]   BEHAVIORAL STRESS POTENTIATES THE BLOOD-PRESSURE EFFECTS OF A HIGH SODIUM-INTAKE [J].
HAYTHORNTHWAITE, JA ;
PRATLEY, RE ;
ANDERSON, DE .
PSYCHOSOMATIC MEDICINE, 1992, 54 (02) :231-239
[10]   PSYCHOSOCIAL HYPERTENSION AND THE DEFENSE AND DEFEAT REACTIONS [J].
HENRY, JP ;
STEPHENS, PM ;
ELY, DL .
JOURNAL OF HYPERTENSION, 1986, 4 (06) :687-697