Differential regulation of corticotropin-releasing factor and vasopressin in discrete brain regions after morphine administration: correlations with hypothalamic noradrenergic activity and pituitary-adrenal response

1997 ◽  
Vol 356 (5) ◽  
pp. 603-610 ◽  
Author(s):  
M. V. Milanés ◽  
M. L. Laorden ◽  
M. Chapleur-Château ◽  
A. Burlet
1987 ◽  
Vol 253 (6) ◽  
pp. R910-R916 ◽  
Author(s):  
C. F. Tsai ◽  
M. T. Lin

This study compared the pain sensitivity, thermal capability, and brain monoamine turnover in normotensive and hypertensive rats. Either the spontaneously hypertensive rats, the experimentally (renal or deoxycorticosterone acetate) hypertensive rats, or their normotensive controls were tested for pain sensitivity by the hot-plate procedure, with the plate maintained at 55 degrees C. The spontaneously hypertensive rats, but not the experimentally hypertensive rats, showed an elevated level of spontaneous pain threshold compared with their appropriate controls. However, both the spontaneously and the experimentally hypertensive rats displayed a reduced sensitivity of analgesic responses to morphine administration. In addition the thermal responses to external stresses in these groups of animals were assessed. It was found that, over an ambient temperature range of 8-30 degrees C, either spontaneously or experimentally hypertensive rats maintained their rectal temperature within a normal limit displayed by their appropriate controls. However, the metabolic rate levels of both spontaneously and experimentally hypertensive rats were elevated at ambient temperatures less than 22 degrees C. Furthermore, compared with their appropriate controls, these hypertensive rats also showed a greater degree of hypothermic responses to chlorpromazine injection. Biochemical examination revealed that either the spontaneously or the experimentally hypertensive rats had a lower serotonin, but a higher catecholamine, turnover in both the hypothalamus and the brain stem compared with their appropriate normotensive controls. The data indicate that, in a hypertensive state, changes in the monoamine turnover of different brain regions may be correlated with the above-mentioned alterations in pain sensitivity and in thermal capability.


2002 ◽  
Vol 399 (1) ◽  
pp. 56-65 ◽  
Author(s):  
Sudarshan C. Upadhya ◽  
Shankar J. Chinta ◽  
Harish V. Pai ◽  
Michael R. Boyd ◽  
Vijayalakshmi Ravindranath

1985 ◽  
Vol 56 (2) ◽  
pp. 121-128 ◽  
Author(s):  
Errol B. De Souza ◽  
Thomas R. Insel ◽  
Marilyn H. Perrin ◽  
Jean Rivier ◽  
Wylie W. Vale ◽  
...  

2006 ◽  
Vol 191 (1) ◽  
pp. 137-145 ◽  
Author(s):  
Yan Zhou ◽  
Jacob Bendor ◽  
Lauren Hofmann ◽  
Matthew Randesi ◽  
Ann Ho ◽  
...  

In this study, we investigated the effects of acute morphine administration, chronic intermittent escalating-dose morphine administration and spontaneous withdrawal from chronic morphine on mRNA levels of mu opioid receptor (MOP-r), and the opioid peptides pro-opiomelanocortin (POMC) and preprodynorphin (ppDyn) in several key brain regions of the rat, associated with drug reward and motivated behaviors: lateral hypothalamus (lat.hyp), nucleus accumbens (NAc) core, amygdala, and caudate–putamen (CPu). There was no effect on MOP-r mRNA levels in these brain regions 30 min after either a single injection of morphine (10 mg/kg, i.p.) or chronic intermittent escalating-dose morphine (from 7.5 mg/kg per day on day 1 up to 120 mg/kg per day on day 10). Activation of the stress-responsive hypothalamic–pituitary–adrenal axis by 12 h withdrawal from chronic morphine was confirmed; both POMC mRNA levels in the anterior pituitary and plasma adrenocorticotropic hormone levels were significantly elevated. Under this withdrawal-related stress condition, there was an increase in MOP-r mRNA levels in the lat.hyp, NAc core, and CPu. Recent studies have demonstrated a novel role for the lat.hyp orexin (or hypocretin) activation in both drug-related positive rewarding, and withdrawal effects. Around 50% of lat.hyp orexin neurons express MOP-r. Therefore, we also examined the levels of lat.hyp orexin mRNA, and found them increased in morphine withdrawal, whereas there was no change in levels of the lat.hyp ppDyn mRNA, a gene coexpressed with the lat.hyp orexin. Our results show that there is an increase in MOP-r gene expression in a region-specific manner during morphine withdrawal, and support the hypothesis that increased lat.hyp orexin activity plays a role in morphine-withdrawal-related behaviors.


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