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γ-氨基丁酸A型受体在神经精神性疾病发生发展中的意义 被引量:7

Significance of GABA_A receptors in the development of some neuropsychiatric diseases
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摘要 γ-氨基丁酸(GABA)是中枢神经系统中介导抑制性突触传递的神经递质,通过GABAA、GABAB和GABAC三种亚型受体介导广泛的生理效应。GABAA受体亚型是GABA受体中占主导地位的亚型,可介导GABA的大部分功能,由来自8个亚基族(α,β,γ,δ,θ,ε,ρ和π)的不同亚基组成,而最典型的GABAA受体结构是由5个异质性多肽亚基(两个α、两个β和一个γ)组成的五边形寡聚体。不同亚基尤其是不同α亚基组成的亚型介导的生理和药理学效应有所不同。GABAB受体对焦虑、抑郁、癫痫以及记忆障碍等不同的神经精神性疾病的发生发展有重要的意义,可能是这些疾病防治药物的作用靶标。 γ-aminobutyric acid( GABA) is an inhibitory neurotransmitter in the central nervous system(CNS), with wide physiological role via GABAA .GABAB and GABAc receptors. GABAA receptor, a dominant type of GABA receptors is comprised of different subunits coming from eight subtmit clusters. Whereas its typical molecular structure is a hetero-pentameric complex, being comprised of two α, two β and one y subunits. And different subunits especially different ~ubunit combinations give rise to various physiological and phannacological effects, which makes GABAA receptor play a great role in the development of some neuropsyehiatric diseases such as anxiety, depression, epilepsy and memory disorders etc. Thus GABAA receptor might be an effective target for preventing these neuropsyehiatrie diseases.
出处 《中国临床药理学与治疗学》 CAS CSCD 2008年第2期208-212,共5页 Chinese Journal of Clinical Pharmacology and Therapeutics
基金 国家自然科学基金资助项目(30470223)
关键词 GABAA受体 药理学效应 神经精神性 疾病 GABAA receptor pharmacological effects neuropsyehiatrie disease
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参考文献17

  • 1Simon J, Wakimoto H, Fujita N, et al. Analysis of the set of GABAA receptor genes in the human genome[J]. Biol Chem,2004,279(40) :41422 - 41435.
  • 2张瑞华,李丽琴,王惠芳,张瑞萍.A型γ氨基丁酸受体结构及其有关药物[J].生命的化学,2003,23(6):441-444. 被引量:12
  • 3Minier F, Sigel E. Positioning of the α subunit isofonns confers a functional signature to & gama aminobutyric acid type A receptors[J]. Proc Natl Acad Sci USA, 2004,101 (20) :7769 - 7774.
  • 4Yoshikawa T, Watanabe A, Ishitsuka Y, et al. Identification of multiple genetic loci linked to the propensity for "behavioral despair" in mice[J]. Genome Res, 2002, 12 (3) :357 - 366.
  • 5Rudolph U, Crestani F, Benke D, et al. Benzodiazepine actions mediated by specific γ-aminobutyric acidA receptor subtypes[J]. Nature, 1999,401 (6755) :796 - 800.
  • 6Sieghart W. GABAA receptors as targets for different classes of drugs[J]. Drugs of the Furture, 2006,31(8):685- 694.
  • 7Houser CR, Esclapez M. Downregulation of the α5 Subunit of the GABAA Receptor in the Pilocarpine Model of Temporal Lobe Epilepsy [ J ]. Hippocampus, 2003,13 (5) : 633 - 645.
  • 8Cossette P, Liu L, Brisebois K, et al. Mutation of GABAR1 in an antosomal dominant form of juvenile myoclonic epilepsy[J]. Nat Genet, 2002,31(2) :184- 189.
  • 9Sarter M, Bnmo JP, Bemtson GG. Psychotogenic properties of benzodiazepine receptor inverse agonists[ J]. Psychopharmacology,2001,156( 1 ) : 1 - 13.
  • 10Wolkowitz OM, Reus VI, Roberts E, et al. Antidepressant and cognition-enhancing effects of DHEA in major depression[J]. Ann NY Acad Sci, 1995,774( 11 ) : 337 - 339.

二级参考文献9

  • 1[1]Collins I et al. Bioorganic & Medicinal Chemistry Letters, 2000, 10:1381-1384
  • 2[2]Ives JH et al. Journal of Neurochemistry, 2002, 80:317-327
  • 3[3]Subramaniam JR et al. Molecular Brain Research, 2001, 92:149-156
  • 4[4]Lancel M et al. Angew Chem Int Ed, 1999, 111:2852-2864
  • 5[5]Jr.L JG et al. Neuropharmacology, 2002, 42:502-521
  • 6[6]Glowa JR et al. Brain Research, 2000, 887:23-33
  • 7[7]Mehta AK et al. Brain Res Rev, 1999, 29:196-217
  • 8[8]Wingrove PB et al. Mol Pharmacol, 1997, 52:874-881
  • 9[9]Krampfl K et al. European J Pharmacology, 2002, 435:1-8

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