Effects of acute or chronic administration of low doses of a dopamine agonist on drinking and locomotor activity in the rat

1981 ◽  
Vol 72 (2) ◽  
pp. 197-202 ◽  
Author(s):  
Colin T. Dourish ◽  
Steven J. Cooper
1986 ◽  
Vol 24 (2) ◽  
pp. 237-240 ◽  
Author(s):  
S. Hjorth ◽  
J.A. Engel ◽  
A. Carlsson
Keyword(s):  

2007 ◽  
Vol 428 (2-3) ◽  
pp. 64-67 ◽  
Author(s):  
Steven A. Gunzler ◽  
Saate Shakil ◽  
Nichole E. Carlson ◽  
John G. Nutt ◽  
Charles K. Meshul
Keyword(s):  

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Zhao-Cai Jiang ◽  
Wei-Jing Qi ◽  
Jin-Yan Wang ◽  
Fei Luo

Previous studies have shown that depressed patients as well as animal models of depression exhibit decreased sensitivity to evoked pain stimuli, and serotonin is indicated to be involved in depression-induced hypoalgesia. The purpose of this study was to investigate the potential role of 5-HT1A receptor in the depression-induced hypoalgesia. Acute or chronic administration of 5-HT1A receptor agonist, 8-OH-DPAT, was performed in olfactory bulbectomy (OB) and sham-operated rats. The depression-like behavior and pain thresholds were measured using open-field test and radiant heat thermal pain test, respectively. We found that acute administration of 8-OH-DPAT increased locomotor activity and pain thresholds in the sham rats but had no effect on the OB rats. In contrast, chronic administration of 8-OH-DPAT reduced locomotor activity and pain thresholds and restored them to normal level. Increased pain thresholds were also observed in the sham rats after the chronic administration. These results demonstrated that chronic administration of 8-OH-DPAT reversed the depression-induced decrease in pain sensitivity in rats, suggesting that 5-HT1A receptor may play a role in the depression-associated hypoalgesia.


1996 ◽  
Vol 312 (2) ◽  
pp. 179-181 ◽  
Author(s):  
Marco Diana ◽  
Anna Lisa Muntoni ◽  
Marco Pistis ◽  
Maria Collu ◽  
Angelo Forgione ◽  
...  

2021 ◽  
Vol 9 (1) ◽  
pp. 72-80
Author(s):  
Silvia G. Ratti ◽  
Osvaldo J. Sacchi ◽  
Edgardo O. Alvarez

In studies from this laboratory, the chronic administration of ZnTe during pregnancy, lactation, and prepuberal stages of litter (F1 generation) modified the behavioral patterns of motivated exploration, lateralized exploration, social activity, and survival responses of maturing rats. To determine whether these affected behaviors would extend to the next generation, F1 litter rats previously exposed to tellurium (Te) up to 30-day-old were left at rest with no further treatment up to 90-day-old. Then, F1 female rats were mated with normal untreated male rats, and in the next generation (F2), the litter rats at 30-day-old preserved the modified behaviors previously observed in their parents. The study revealed that Te effects were intergenerational. Here, considering that ZnTe was used in the previous study and that Zn ion has many physiological functions in the cell, experiments were conducted to elucidate if Zn would have an intergenerational effect similar to Te. Working with the same experimental setup as in the previous study but using ZnCl2 instead of ZnTe, results revealed that none of the behavioral responses studied were affected by the F1 generation. However, in the F2 generation, lateralized exploration and survival behavior were inhibited, suggesting that Zn also has an intergenerational effect.


Sign in / Sign up

Export Citation Format

Share Document