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不同品系小鼠对mCPP诱导焦虑样行为的差异研究 被引量:3

Differences in anxiety-related behavior induced by mCPP and responses to diazepam in two strains of mice
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摘要 目的:评价BALB/c和ICR小鼠对1-(3-氯苯基)哌嗪单盐酸盐(mCPP)诱导焦虑样行为的差异。方法:将两品系小鼠各分为四组:生理盐水对照组、mCPP焦虑组、地西泮对照组和地西泮+mCPP组。行为学检测前30min腹腔注射地西泮、皮下注射mCPP,采用开场实验、明暗穿箱和高架十字迷宫比较两品系小鼠焦虑样行为的差异。结果:地西泮使焦虑的BALB/c小鼠中央路程比值和中央时间比值增加,对ICR小鼠无作用;两品系小鼠运动总路程有差异。地西泮使焦虑小鼠进入暗箱潜伏期延长、明暗穿箱次数增加、暗箱滞留时间缩短,BALB/c小鼠对地西泮的反应比ICR小鼠更敏感。地西泮可使焦虑小鼠开臂进入次数百分比、开臂停留时间百分比和开臂探臂时间百分比增加,两品系小鼠仅在开臂停留时间和开臂探臂时间上有差异。结论:mCPP诱导焦虑小鼠比正常小鼠对地西泮的敏感性高;BALB/c小鼠焦虑水平较低,探究能力和风险评估能力较高,是抗焦虑药物研究中可供选择的较合适的动物品系。 AIM: To compare the differences in anxietyrelated behavior induced by chloro phenylpiperazinehydrochloride (mCPP) and re sponse to diazepam in BALB/c mice and ICR mice. METHODS: Each were divided into four groups: saline group, mCPP group, diazepam group and (diazepam+mCPP) group. Diazepam was administrated intraperitoneally and mCPP was administrated subcutaeously 30 rain before behavioral test. Openfield test, lightdark tran sition test and elevated plus maze test were used. RESULTS: In openfield test, the central distance ratio and the central time ratio were in creased in the (diazepam Jr mCPP) group of BALB/c mice. But there were no effects on ICR mice. Only was there significant difference on to tal distance between two mice strains. In light dark transition test, latency into dark box and number of transitions were increased, and time ratio in dark box was decreased in (diazepam+mCPP) group of two strains mice. The response to diazepam was were more sensitive in BALB/c mice than ICR mice. Number of openarm en tries, time and exploring time ratio in openarm in the elevated plus maze all increased in diaze pamqmCPP) group of two strains mice. There were differences of time and exploring time in openarm between them. CONCLUSION: The re sponse to diazepam is more sensitive in anxiety mice than normal mice. BALB/c mice have low level of anxiety, high baseline exploration and risk assessment of a new environment, which is a suitable mice strain to develop anxiolytic drugs.
出处 《中国临床药理学与治疗学》 CAS CSCD 2013年第11期1238-1243,共6页 Chinese Journal of Clinical Pharmacology and Therapeutics
基金 浙江省卫生厅科研基金资助项目(2010KYA011) 2012年浙江省大学生科技创新活动计划(新苗人才计划)(2012R434002) 浙江医学高等专科学校2011年度科研基金项目(学生项目)(2011XX01)
关键词 焦虑 地西泮 品系差异 小鼠 l-(3-氯 苯基)哌嗪单盐酸盐 Anxiety Strain difference Dia-zepam Mice Chlorophenylpiperazinehydro-chloride (mCPP)
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  • 1Miller SM, Piasecki CC, Lonstein JS. Use of the light-dark box to compare the anxiety-related be havior of virgin and postpartum female rats [J]. Pharmacol Biochem Behav, 2011, 100 (1): 130 - 137.
  • 2Chatterjee M, Verma R, Lakshmi V, et al. Anxio lytic effects of plumeria rubra var. acutifolia (Poiret) L. flower extracts in the elevated Plus maze model of anxiety in mice[J]. Asian J Psyehiatr, 2013, 6(2): 113-118.
  • 3Enkel T, Thomas M. Bartsch D. Differential effects of subchronic pheneyclidine on anxiety in the light- enhanced startle-, light/dark exPloration- and open field tests[J]. Behav Brain Res, 2013, 243(5):61 -65.
  • 4Hajikhani R, Ahmadi A, Naderi N, et al. Effect of phencyclidine derivatives on anxiety-like behavior u- sing an elevated-plus maze test in mice[J]. Adv Clin Exp Med, 2013, 21(3): 307-312.
  • 5van Gaalen MM, Steckler T. Behavioural analysis of four mouse strains in an anxiety test battery[J]. Behav Brain Res, 2000, 115(1): 95-106.
  • 6Roman E, Meyerson BJ, Hyytia P, et al. The mul tivariate concentric square field test reveals differ ent behavioural profiles in male AA and ANA rats with regard to risk taking and environmental reac tivity[J]. Behav Brain Res, 2007, 183(2): 195-205.
  • 7Bagdy G, Graf M, Anheuer ZE, et al. Anxiety-like effects induced by acute fluoxetine, sertraline or mCPP treatment are reversed by pretreatment with the 5-HT2C receptor antagonist SB-242084 but not the 5-HTIA receptor antagonist WAY-100635[J]. Int J Neuropsychopharmacol, 2001, 4(4): 399-408.
  • 8Mamiya T, Asanuma T, Kawai Y, et al. Effects of soybean food pellets on mCPP-induced anxiety model of mice[J]. Biol Pharm Bull, 2006, 29(7) 1498-1500.
  • 9Peng WH, Hsieh MT, Lee YS, et al. Anxiolytic effect of seed of Ziziphus jujuba in mouse models of anxiety[J]. J Ethnopharmacol, 2000, 72(3): 435-441.
  • 10Van Veen JF, Van der Wee NJ, Fiselier J, et al. Behavioural effects of rapid intravenous administra tion of meta-chlorophenylpiperazine (mCPP) in pa tients with generalized social anxiety disorder, panic disorder and healthy controls[J]. Eur Neuropsycho pharmacol, 2007, 17(10): 637-642.

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  • 1Golub Y, Kaltwasser SF, Mauch CP,et al. Reduced hippocampus vol- ume in the mouse model of Posttraumatic Stress Disorder [ J ]. J Psy- chiatr Res,2011,45 (5) : 650-659.
  • 2Xue X,Shao S, Li M, et al. Maternal separation induces alterations of serotonergic system in different aged rats[ J]. Brain Res Bull,2013, 95 : 15-20.
  • 3Nithianantharajah J, Hannan AJ. Enriched environments, experience- dependent plasticity and disorders of the nervous system[ J]. Nat Rev Neurosci,2006,7(9) : 697-709.
  • 4Veena J, Srikumar BN, Raju TR, et al. Exposure to enriched environ- ment restores the survival and differentiation of new born cells in the hippocampus and ameliorates depressive symptoms in chronically stressed rats [ J ]. Neuroscience Lett, 2009,455 ( 3 ) : 178-182.
  • 5Yamamoto S, Morinobu S, Takei S, et al.Single prolonged stress: to- ward an animal model of posttraumatic stress disorder [ J ]. Depress Anxiety,2009,26(12) :1110-1117.
  • 6Urakawa S, Takamoto K, Hori E, et al. Rearing in enriched environ- ment increases parvalbumin-positive small neurons in the amygdala and decreases anxiety-like behavior of male rats [ J ]. BMC Neurosei, 2013,14(1) :13.
  • 7Hendriksen H, Prins J, Olivier B, et al. Environmental enrichment in- duces behavioral recovery and enhanced hippocampal cell proliferation in an antidepressant-resistant animal model for PTSD [ J ]. PLoS One, 2010,5(8) :el 1943.
  • 8Mura T, Proust-Lima C, Akbaraly T, et al. Chronic use of benzodiazepines and latent cognitive decline in the elderly: results from the Three-city study [ J ]. Eur Neuropsychopharmacol, 213, 23 (3) :212-223.
  • 9Nkogho Mengte PG, ous B, Berbiche D, et al. Benzodiazepine depeqderwe and the risk of depression and anxiety disorders : seniors" health study [ J ]. En- cephale, 2014, 40 (3) :216-222.
  • 10Willems IA, Gorgels WJ, Oude Voshaar RC, et al. Tolerance to benzodiazepines among long-term users in primary care [ J ]. Farn Pract, 2013, 30 ( 4 ) : 404- 410.

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