Effects of neonatal handling on the behavior and prolactin stress response in male and female rats at various ages and estrous cycle phases of females

2004 ◽  
Vol 81 (3) ◽  
pp. 489-498 ◽  
Author(s):  
G SEVERINO ◽  
I FOSSATI ◽  
M PADOIN ◽  
C GOMES ◽  
L TREVIZAN ◽  
...  
Neuroscience ◽  
2006 ◽  
Vol 142 (2) ◽  
pp. 305-314 ◽  
Author(s):  
S. Pondiki ◽  
A. Stamatakis ◽  
A. Fragkouli ◽  
H. Philippidis ◽  
F. Stylianopoulou

2007 ◽  
Vol 1154 ◽  
pp. 144-153 ◽  
Author(s):  
Therese A. Kosten ◽  
Hongjoo J. Lee ◽  
Jeansok J. Kim

2013 ◽  
pp. S99-S108 ◽  
Author(s):  
R. ŠLAMBEROVÁ ◽  
E. MACÚCHOVÁ ◽  
K. NOHEJLOVÁ-DEYKUN ◽  
B. SCHUTOVÁ ◽  
L. HRUBÁ ◽  
...  

The aim of the present study was to compare the response to acute application of several drugs in adult male and female rats prenatally exposed to methamphetamine (MA). Spontaneous locomotor activity and exploratory behavior of adult male and female rats prenatally exposed to MA (5 mg/kg) or saline were tested in a Laboras apparatus (Metris B.V., Netherlands) for 1 h. Challenge dose of the examined drug [amphetamine – 5 mg/kg; cocaine – 5mg/kg; MDMA (3,4-methylenedioxymethamphetamine) – 5 mg/kg; morphine – 5 mg/kg; THC (delta9-tetrahydrocannabinol) – 2 mg/kg] or saline was injected prior to testing. Our data demonstrate that prenatal MA exposure did not affect behavior in male rats with cocaine or morphine treatment, but increased locomotion and exploration in females. Application of amphetamine and MDMA in adulthood increased activity in both sexes, while cocaine and THC only in female rats. Morphine, on the other hand, decreased the activity in the Laboras test in both sexes. As far as sex and estrous cycle is concerned, the present study shows that males were generally less active than females and also females in proestrus-estrus phase of the estrous cycle were more active than females in diestrus. In conclusion, the present study shows that the prenatal MA exposure does not induce general sensitization but affects the sensitivity to drugs dependently to mechanism of drug action and with respect to gonadal hormones.


2016 ◽  
Vol 70 ◽  
pp. 206-216 ◽  
Author(s):  
Russell D. Romeo ◽  
Ravenna Patel ◽  
Laurie Pham ◽  
Veronica M. So

1994 ◽  
Vol 55 (5) ◽  
pp. 971-974 ◽  
Author(s):  
James W. Smythe ◽  
Cheryl M. McCormick ◽  
Joseph Rochford ◽  
Michael J. Meaney

1989 ◽  
Vol 257 (4) ◽  
pp. R738-R743 ◽  
Author(s):  
J. T. Crofton ◽  
L. Share

To examine the osmotic control of vasopressin release, hypertonic saline was infused in conscious unrestrained male rats and female rats in each phase of the estrous cycle. The progressive increase in plasma osmolality was accompanied by a progressive increase in the plasma vasopressin concentration, but the magnitude of the former was smaller in metestrus than in other phases of the cycle and in males (P less than 0.01). The osmotic threshold for vasopressin release was higher in males than in females in each phase of the estrous cycle (P less than 0.05 to P less than 0.01), but the sensitivity of the osmotic control of vasopressin release was similar in male and female rats. Although the pressor response to hypertonic saline was greater in estrous females than in the other females (P less than 0.05 to P less than 0.01), the reduction in blood pressure, after a V1 antagonist 30 min after starting the hypertonic saline infusion, was similar in males and females. Thus there are gender-related differences in the osmotic control of vasopressin release and, in females, cycle-dependent differences in the cardiovascular responses to hypertonic saline.


Endocrinology ◽  
2010 ◽  
Vol 151 (6) ◽  
pp. 2689-2699 ◽  
Author(s):  
A. C. Kentner ◽  
S. A. McLeod ◽  
E. F. Field ◽  
Q. J. Pittman

Inflammatory molecules, such as cyclooxygenase (COX), a prostaglandin synthetic enzyme, have been identified as a marker of depressive symptomology. Previously, we have observed elevated basal COX-2 expression in the hypothalamus of adult male rats treated neonatally with lipopolysaccharide (LPS), which might suggest a phenotype for disrupted hedonic behavior, a symptom of depression. However, COX-2 and its contribution to the expression of anhedonic behavior has not been investigated in these males or in female rats across the estrous cycle, which is the purpose of the current work. Here, we examine the effects of a neonatal LPS challenge or saline on the sucrose preference test as a measure of anhedonia, and hypothalamic COX-2 expression, in adult male and freely cycling female rats. Our data indicate a sex difference in that neonatal LPS at postnatal d 14 causes elevated basal expression of hypothalamic COX-2 in male, but not in female, rats. Additionally, baseline sucrose preference in male and female rats was unaltered as a function of neonatal LPS treatment or estrous cycle stage. In both male and female animals, 50 μg/kg LPS in adulthood caused elevated plasma IL-6 and hypothalamic COX-2 expression in neonatally saline-treated rats but significantly less so in neonatally LPS-treated rats of both sexes; this neonatal programming was not evident for sucrose preference or for total fluid intake (even after much higher doses of LPS). Our data are suggestive of a dissociation between inflammation and anhedonic behavior and a differential effect of neonatal inflammation in males and females.


1976 ◽  
Vol 71 (1) ◽  
pp. 47-50 ◽  
Author(s):  
J. D. DUNN ◽  
M. E. HESS

SUMMARY The influence of thyroid hormones on pituitary–adrenal function was assessed by studying several aspects of adrenocortical function approximately 30 days after thyroparathyroidectomy (TPTx). Both male and female rats showed evidence of rhythmic adrenocortical activity; peak plasma corticosterone levels occurred just before the dark phase of the lighting schedule. Only the amplitude of the rhythm appeared altered by TPTx. Peak plasma corticosterone levels in TPTx male and female animals were less (P < 0·05) than corresponding levels in intact control rats. Both sexes showed significant responses to stress, but the morning stress response in TPTx females was less (P < 0·01) than the stress response in intact controls. Concomitant with the reduced stress response, the adrenocortical response to exogenous ACTH was reduced in TPTx female rats.


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