4.7 Review

The role of dopamine receptors in the neurotoxicity of methamphetamine

期刊

JOURNAL OF INTERNAL MEDICINE
卷 273, 期 5, 页码 437-453

出版社

WILEY
DOI: 10.1111/joim.12049

关键词

amphetamine derivatives; designer drugs; dopamine; drug addiction; Parkinson's disease; psychostimulants

资金

  1. Spanish Ministry of Ciencia e Innovacion [BFU2010-20664]
  2. Spanish Ministry of Economia y Competitividad
  3. Spanish Ministry of Sanidad, Servicios Socales e Igualdad
  4. ISCIII
  5. PNSD RedRTA [RD06/0001/1011]
  6. CIBERNED [CB06/05/0055]
  7. Comunidad de Madrid [S2011/BMD-2336]
  8. Juan de la Cierva postdoctoral fellowship
  9. JAE predoctoral fellowship

向作者/读者索取更多资源

Ares-Santos S, Granado N, Moratalla R (Instituto Cajal, Consejo Superior de Investigaciones Cientificas, CSIC, Madrid; CIBERNED, ISCIII, Madrid; Universidad Complutense de Madrid, Madrid, Spain). The role of dopamine receptors in the neurotoxicity of methamphetamine.(Review). J InternMed 2013; 273: 437-453. Methamphetamine is a synthetic drug consumed by millions of users despite its neurotoxic effects in the brain, leading to loss of dopaminergic fibres and cell bodies. Moreover, clinical reports suggest that methamphetamine abusers are predisposed to Parkinson's disease. Therefore, it is important to elucidate the mechanisms involved in methamphetamine-induced neurotoxicity. Dopamine receptors may be a plausible target to prevent this neurotoxicity. Genetic inactivation of dopamine D1 or D2 receptors protects against the loss of dopaminergic fibres in the striatum and loss of dopaminergic neurons in the substantia nigra. Protection by D1 receptor inactivation is due to blockade of hypothermia, reduced dopamine content and turnover and increased stored vesicular dopamine in D1R(-/-) mice. However, the neuroprotective impact of D2 receptor inactivation is partially dependent on an effect on body temperature, as well as on the blockade of dopamine reuptake by decreased dopamine transporter activity, which results in reduced intracytosolic dopamine levels in D2R(-/-) mice.

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