scholarly journals Oxycodone-induced conditioned place preference and sensitization of locomotor activity in adolescent and adult mice

2013 ◽  
Vol 110 ◽  
pp. 112-116 ◽  
Author(s):  
Keiichi Niikura ◽  
Ann Ho ◽  
Mary Jeanne Kreek ◽  
Yong Zhang
Keyword(s):  
Locomotor Activity ◽  
Conditioned Place Preference ◽  
Place Preference ◽  
Adult Mice

scholarly journals S15-2Effects of environmental enrichment upon ethanol-induced conditioned place preference and BDNF levels in adolescent and adult mice

2017 ◽  
Vol 52 (suppl_1) ◽  
pp. i4-i30
Author(s):  
R Camarini ◽  
A.B. Suárez ◽  
L.B. Hoffmann ◽  
A.V. Rueda ◽  
M.B. Rae ◽  
...  
Keyword(s):  
Conditioned Place Preference ◽  
Environmental Enrichment ◽  
Place Preference ◽  
Adult Mice

The Effect of Dihydromyricetin, a Natural Flavonoid, on Morphine-induced Conditioned Place Preference and Physical Dependence in Mice

Drug Research ◽  
2020 ◽  
Vol 70 (09) ◽  
pp. 410-416
Author(s):  
Leila Etemad ◽  
Hadi Farkhari ◽  
Mohaddeseh Sadat Alavi ◽  
Ali Roohbakhsh
Keyword(s):  
Locomotor Activity ◽  
Animal Models ◽  
Conditioned Place Preference ◽  
Gabaa Receptors ◽  
Physical Dependence ◽  
Place Preference ◽  
Morphine Dependence ◽  
Male Mice ◽  
Alcohol Hangover ◽  
Withdrawal Signs

Abstract Objective Dihydromyricetin (DHM), a natural flavonoid, is used to reduce alcohol hangover. It has a modulatory role on GABAA receptors with significant effects on seizure and anxiety in animal models. We aimed to evaluate the effect of DHM on morphine conditioned place preference (CPP) and withdrawal sings following morphine dependence using animal models. Methods The effect of DHM (1, 2 and 5 mg/kg, intraperitoneal; ip) on the acquisition and expression of morphine-induced CPP was evaluated in male mice. Administration of morphine for three consecutive days induced physical dependence. The withdrawal signs such as jumping and defecation were precipitated by administration of naloxone (8 mg/kg, ip). The effect of DHM on the development of physical dependence was assessed by injection of DHM before morphine administrations. Results DHM, at the dose of 5 mg/kg, reduced expression of morphine CPP with an increase in the locomotor activity. DHM, at the doses of 2 and 5 mg/kg, also reduced development of morphine CPP. DHM alleviated development of morphine-induced physical dependence at the dose of 1, 2, and 5 mg/kg by decreasing jumping and defecation. Conclusion These results indicated that DHM decreased acquisition and expression of morphine CPP and inhibited development of morphine-induced physical dependence.

Diverging frequency-modulated 50-kHz vocalization, locomotor activity and conditioned place preference effects in rats given repeated amphetamine treatment

2014 ◽  
Vol 83 ◽  
pp. 128-136 ◽  
Author(s):  
Ewa Taracha ◽  
Ewelina Kaniuga ◽  
Stanisław J. Chrapusta ◽  
Piotr Maciejak ◽  
Lech Śliwa ◽  
...  
Keyword(s):  
Locomotor Activity ◽  
Conditioned Place Preference ◽  
Place Preference ◽  
Amphetamine Treatment

scholarly journals α-Conotoxin TxID and [S9K]TxID, α3β4 nAChR Antagonists, Attenuate Expression and Reinstatement of Nicotine-Induced Conditioned Place Preference in Mice

Marine Drugs ◽  
2020 ◽  
Vol 18 (12) ◽  
pp. 646
Author(s):  
Xiaodan Li ◽  
Shen You ◽  
Jian Xiong ◽  
Yamin Qiao ◽  
Jinpeng Yu ◽  
...  
Keyword(s):  
Smoking Cessation ◽  
Locomotor Activity ◽  
Conditioned Place Preference ◽  
Addiction Treatment ◽  
Nicotine Addiction ◽  
Place Preference ◽  
Inhibition Activity ◽  
Nicotinic Acetylcholine ◽  
The World ◽  
Superior Effect

Tobacco smoking has become a prominent health problem faced around the world. The α3β4 nicotinic acetylcholine receptor (nAChR) is strongly associated with nicotine reward and withdrawal symptom. α-Conotoxin TxID, cloned from Conus textile, is a strong α3β4 nAChR antagonist, which has weak inhibition activity of α6/α3β4 nAChR. Meanwhile, its analogue [S9K]TxID only inhibits α3β4 nAChR (IC50 = 6.9 nM), and has no inhibitory activity to other nAChRs. The present experiment investigates the effect of α3β4 nAChR antagonists (TxID and [S9K]TxID) on the expression and reinstatement of nicotine-induced conditioned place preference (CPP) and explores the behaviors of acute nicotine in mice. The animal experimental results showed that TxID and [S9K] TxID could inhibit the expression and reinstatement of CPP, respectively. Moreover, both had no effect in acute nicotine experiment and the locomotor activity in mice. Therefore, these findings reveal that the α3β4 nAChR may be a potential target for anti-nicotine addiction treatment. [S9K]TxID, α3β4 nAChR antagonist, exhibit a superior effect for anti-nicotine addiction, which is promising to develop a novel smoking cessation drug.

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