TY - JOUR
T1 - Reevaluation of anti-obesity action of mazindol and elucidation of its effect on the reward system
AU - Aotani, Daisuke
AU - Son, Cheol
AU - Shimizu, Yoshiyuki
AU - Nomura, Hidenari
AU - Hikida, Takatoshi
AU - Kusakabe, Toru
AU - Tanaka, Tomohiro
AU - Miyazawa, Takashi
AU - Hosoda, Kiminori
AU - Nakao, Kazuwa
N1 - Funding Information:
This work was supported in part by Grant-in-Aid for Scientific Research JSPS KAKENHI Grant Numbers 23591307, 21229013, 25293211, 15H04275, 16K14579, and 16H06568 ; research grants from the Ministry of Education, Culture, Sports, Science and Technology of Japan ; and grants from the Smoking Research Foundation .
Funding Information:
K. Nakao received grants from FUJIFILM Pharma Co., Ltd. , and D. Aotani and K. Nakao received lecturer’s fees from FUJIFILM Pharma Co., Ltd .
Publisher Copyright:
© 2016 Elsevier Ireland Ltd
PY - 2016/10/28
Y1 - 2016/10/28
N2 - In this study, we evaluated the preventive effect of mazindol on the development of obesity and sought to elucidate the drug's effects on the reward system. In mice, body weight gain and hyperphagia induced by high-fat diet (HFD) were decreased by 38.6% and 13.9%, respectively, by subcutaneous infusion of mazindol (1.5 mg/kg/day) for 28 days. A single intraperitoneal administration of mazindol (1.5 mg/kg) significantly reduced lipid preference, as assessed using the two-bottle preference paradigm (vehicle, 89.98 ± 1.66%; mazindol, 75.65 ± 5.47%; p < 0.05). In addition, the conditioned place preference (CPP) test demonstrated that mazindol (1.5 mg/kg) significantly decreased CPP score for HFD as compared with vehicle (vehicle, 330.44 ± 58.61 s; mazindol, 144.72 ± 43.02 s; p < 0.05). Moreover, at the dose required for these effects, mazindol did not elicit abuse potential or induce psychostimulant-like behavior. These results confirm that mazindol prevents diet-induced obesity without addictive behavior and demonstrate that its action is mediated at least in part via the reward system, advancing our understanding of mazindol in clinical practice.
AB - In this study, we evaluated the preventive effect of mazindol on the development of obesity and sought to elucidate the drug's effects on the reward system. In mice, body weight gain and hyperphagia induced by high-fat diet (HFD) were decreased by 38.6% and 13.9%, respectively, by subcutaneous infusion of mazindol (1.5 mg/kg/day) for 28 days. A single intraperitoneal administration of mazindol (1.5 mg/kg) significantly reduced lipid preference, as assessed using the two-bottle preference paradigm (vehicle, 89.98 ± 1.66%; mazindol, 75.65 ± 5.47%; p < 0.05). In addition, the conditioned place preference (CPP) test demonstrated that mazindol (1.5 mg/kg) significantly decreased CPP score for HFD as compared with vehicle (vehicle, 330.44 ± 58.61 s; mazindol, 144.72 ± 43.02 s; p < 0.05). Moreover, at the dose required for these effects, mazindol did not elicit abuse potential or induce psychostimulant-like behavior. These results confirm that mazindol prevents diet-induced obesity without addictive behavior and demonstrate that its action is mediated at least in part via the reward system, advancing our understanding of mazindol in clinical practice.
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U2 - 10.1016/j.neulet.2016.09.014
DO - 10.1016/j.neulet.2016.09.014
M3 - Article
C2 - 27658895
AN - SCOPUS:84988653926
SN - 0304-3940
VL - 633
SP - 141
EP - 145
JO - Neuroscience Letters
JF - Neuroscience Letters
ER -