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伐尼克兰不会增加尼古丁依赖患者的血清脑源性神经营养因子水平。

Varenicline does not increase serum BDNF levels in patients with nicotine dependence.

作者信息

Umene-Nakano Wakako, Yoshimura Reiji, Yoshii Chiharu, Hoshuyama Tsutomu, Hayashi Kenji, Hori Hikaru, Katsuki Asuka, Ikenouchi-Sugita Atsuko, Nakamura Jun

机构信息

Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka, Japan.

出版信息

Hum Psychopharmacol. 2010 Apr;25(3):276-9. doi: 10.1002/hup.1113.

Abstract

Varenicline, alpha4beta2 nicotinic acetylcholine receptor (nAChR) partial agonist, is a new class of medications for treating nicotine dependence. As an alpha4beta2 nAChR partial agonist, varenicline serves to reduce nicotine withdrawal symptoms, while high-affinity binding of the agonist mitigates the reinforcing effects of smoking. In the present study, we compared serum brain-derived neurotrophic factor (BDNF) levels of nicotine dependence and nonsmokers, and we investigated changes in serum BDNF levels after 8 weeks of treatment with varenicline. Patients met the DSM-IV criteria for nicotine dependence. Both the Fagerström test for nicotine dependence (FTND) and the Tobacco Dependence Screener (TDS) were used. Serum BDNF levels and breath carbon monoxide (CO) levels were measured before and 8 weeks after varenicline treatment. Fourteen of 16 subjects (87.5%) stopped smoking within 12 weeks of varenicline treatment. Thirteen healthy nonsmokers who never had previously smoked were randomly selected as a control group. Serum BDNF levels of patients before treatment (4.8 +/- 3.8 ng/ml) were significantly lower than those in the control group (12.4 +/- 6.13 ng/ml). Serum BDNF levels had not increased from baseline (4.8 +/- 3.8 ng/ml) to 8 weeks after varenicline treatment (3.0 +/- 1.1 ng/ml) of patients. These results suggest that smoking might decrease serum BDNF levels and that treatment with varenicline for 8 weeks, combined with 12 weeks of not smoking, does not increase serum BDNF levels in smokers.

摘要

伐尼克兰,一种α4β2烟碱型乙酰胆碱受体(nAChR)部分激动剂,是一类用于治疗尼古丁依赖的新型药物。作为一种α4β2 nAChR部分激动剂,伐尼克兰可减轻尼古丁戒断症状,同时该激动剂的高亲和力结合可减轻吸烟的强化作用。在本研究中,我们比较了尼古丁依赖者和非吸烟者的血清脑源性神经营养因子(BDNF)水平,并研究了伐尼克兰治疗8周后血清BDNF水平的变化。患者符合DSM-IV尼古丁依赖标准。使用了尼古丁依赖的Fagerström测试(FTND)和烟草依赖筛查工具(TDS)。在伐尼克兰治疗前及治疗8周后测量血清BDNF水平和呼出气一氧化碳(CO)水平。16名受试者中有14名(87.5%)在伐尼克兰治疗的12周内戒烟。随机选择13名从未吸烟的健康非吸烟者作为对照组。治疗前患者的血清BDNF水平(4.8±3.8 ng/ml)显著低于对照组(12.4±6.13 ng/ml)。患者从伐尼克兰治疗前的基线水平(4.8±3.8 ng/ml)到治疗8周后(3.0±1.1 ng/ml)血清BDNF水平并未升高。这些结果表明,吸烟可能会降低血清BDNF水平,并且伐尼克兰治疗8周并结合12周不吸烟,并不会使吸烟者的血清BDNF水平升高。

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