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Qing Chang

Dongfang Hospital, Beijing University of Chinese Medicine, No.6 Fangxingyuan Fengtai District, Beijing, 100078, China. Changqing-0318@163.com.

2 papers in the library · 26 citations · publishing 2015

Papers

Noribogaine reduces nicotine self-administration in rats.

Journal of psychopharmacology (Oxford, England) June 1, 2015 Qing Chang, Taleen Hanania, Deborah C Mash et al. 26 citations

Noribogaine, a drug that acts on opioid receptors, nicotinic receptors, and serotonin transporters, was tested for its ability to reduce nicotine self-administration in adult male rats. After training to self-administer nicotine intravenously, rats received oral doses of noribogaine (12.5, 25, or 50 mg/kg), vehicle, varenicline, or saline. Noribogaine dose-dependently decreased nicotine self-administration by up to 64% compared to saline-treated levels, matching the effectiveness of 1.7 mg/kg varenicline. At the highest dose, noribogaine reduced food pellet self-administration by only 23%, indicating greater specificity for nicotine. The findings suggest noribogaine may be a promising treatment for nicotine dependence.

Characterization of Noribogaine at nAChRs and Effect on Nicotine Self‐Administration in Rats

The FASEB Journal April 1, 2015 Émeline L. Maillet, Qing Chang, Nicolas Milon et al.

Noribogaine, a drug that acts on opioid receptors, nicotinic receptors, and serotonin transporters, was tested for its effects on nicotine dependence. It inhibited several types of nicotinic acetylcholine receptors, including α3β4 and α7. In a rat model of nicotine self-administration, noribogaine dose-dependently reduced nicotine intake by up to 64% compared to saline-treated rats, an effect comparable to the approved smoking cessation drug varenicline. These results suggest noribogaine may have potential for treating smoking cessation, substance abuse, and anxiety disorders.