Effect of progesterone on serotonin turnover in rats primed with estrogen implants into the ventromedial hypothalamus

1993 ◽  
Vol 32 (3) ◽  
pp. 293-300 ◽  
Author(s):  
Robert W. Gereau ◽  
Kathleen A. Kedzie ◽  
Kenneth J. Renner
1987 ◽  
Vol 18 (2) ◽  
pp. 153-158 ◽  
Author(s):  
Joseph D. Bast ◽  
Carol Hunts ◽  
Kenneth J. Renner ◽  
Ramona K. Morris ◽  
David M. Quadagno

Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 216-OR
Author(s):  
QI WANG ◽  
BICHEN ZHANG ◽  
YUNFAN YANG ◽  
JIA MI ◽  
GENG TIAN ◽  
...  

Diabetes ◽  
1995 ◽  
Vol 44 (2) ◽  
pp. 180-184 ◽  
Author(s):  
W. P. Borg ◽  
R. S. Sherwin ◽  
M. J. During ◽  
M. A. Borg ◽  
G. I. Shulman

2009 ◽  
Vol 19 ◽  
pp. S264-S265
Author(s):  
R.L. Freitas ◽  
M.A. Castiblanco-Urbina ◽  
A. Uribe-Mariño ◽  
D.H. Elias-Filho ◽  
N.C. Coimbra

1983 ◽  
Vol 98 (1) ◽  
pp. 7-17 ◽  
Author(s):  
R. F. Walker

In ovariectomized rats treated chronically with oestrogen there is a loss of positive feedback effects on LH secretion. This was not due to depletion of pituitary LH since injection of LH releasing hormone (LH-RH; 50 ng/100 g body wt) caused a significant (P < 0·01) rise in serum LH even after the loss of spontaneous LH surges. However, the magnitude of the increase in serum LH in response to LH-RH was greater (412 ± 41 μg/l) before than after (291 ± 29 μg/l) loss of the LH surges. Excessive blood sampling was also not responsible, since positive feedback responses declined comparably in rats bled daily or once every 3–4 days. Progesterone (0·5 mg s.c.), administered for 5 consecutive days, failed to restore LH surges indicating that deficiency of this steroid after ovariectomy does not cause positive feedback responses to disappear in rats exposed chronically to oestrogen. Moreover regular daily fluctuations in serum progesterone, probably of adrenal origin, occurred before as well as after daily LH surges were lost. Serotonin content and turnover were depressed (P < 0·05) when ovariectomized rats first received the subcutaneous capsules containing oestrogen. This change correlated temporally with the onset of daily LH surges and was eventually lost. After 30 days exposure to oestrogen, serotonin turnover increased (P < 0·01) and positive feedback responses were absent. Catecholamine levels and turnover did not show differential responses to oestrogen and were depressed after acute as well as chronic steroid treatment. p-Chlorophenylalanine (pCPA; 250 mg/kg)+ l-dihydroxyphenylalanine (l-DOPA; 200 mg/kg), which depress serotonin and enhance catecholamine synthesis respectively, failed to reinstate LH surges, but these were restored in 22% of the rats receiving l-DOPA alone. pCPA, followed 2 days later by 5-hydroxytryptophan (5-HTP) at 11.00 h, reinstated LH surges in 88% of rats, and a dose–response curve showed that as little as 4 mg 5-HTP/kg stimulated repetitive LH surges when given with pCPA according to this schedule. However, the administration of α-methyl-p-tyrosine + l-DOPA, an analogous treatment involving catecholamines, was only marginally effective (15%). These findings suggest that perturbations of monoamine metabolism occurring in ovariectomized rats exposed to oestrogen for several weeks contribute to loss of daily LH surges. Since pCPA + 5-HTP restored LH surges most effectively, then positive feedback may disappear as the facilitatory effect of serotonin is lost after chronic oestrogen administration.


Synapse ◽  
2013 ◽  
Vol 68 (3) ◽  
pp. 127-130 ◽  
Author(s):  
Helene Bach ◽  
Yung-Yu Huang ◽  
Mark D. Underwood ◽  
Andrew J. Dwork ◽  
J. John Mann ◽  
...  

2021 ◽  
pp. 097275312110057
Author(s):  
Archana Gaur ◽  
G.K. Pal ◽  
Pravati Pal

Background: Obesity is because of excessive fat accumulation that affects health adversely in the form of various diseases such as diabetes, hypertension, cardiovascular diseases, and many other disorders. Our Indian diet is rich in carbohydrates, and hence the sucrose-induced obesity is an apt model to mimic this. Ventromedial hypothalamus (VMH) is linked to the regulation of food intake in animals as well as humans. Purpose: To understand the role of VMHin sucrose-induced obesity on metabolic parameters. Methods: A total of 24 adult rats were made obese by feeding them on a 32% sucrose solution for 10 weeks. The VMH nucleus was ablated in the experimental group and sham lesions were made in the control group. Food intake, body weight, and biochemical parameters were compared before and after the lesion. Results: Male rats had a significant weight gain along with hyperphagia, whereas female rats did not have a significant weight gain inspite of hyperphagia. Insulin resistance and dyslipidemia were seen in both the experimental and control groups. Conclusion: A sucrose diet produces obesity which is similar to the metabolic syndrome with insulin resistance and dyslipidemia, and a VMH lesion further exaggerates it. Males are more prone to this exaggeration.


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