4.7 Article

Tetrahydroberberine blocks ATP-sensitive potassium channels in dopamine neurons acutely-dissociated from rat substantia nigra pars compacta

期刊

NEUROPHARMACOLOGY
卷 59, 期 7-8, 页码 567-572

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuropharm.2010.08.018

关键词

Tetrahydroberberine; Dopaminergic neurons; Substantia nigra compacta; ATP-sensitive K+ channel; Rotenone; Parch-clamp

资金

  1. 973-project, China [2009CB52200]
  2. CNSF, China [30825042]

向作者/读者索取更多资源

Tetrahydroberberine (THB) exhibits neuroprotective effects but its targets and underlying mechanisms are largely unknown. Emerging evidence indicates that ATP-sensitive potassium (K-ATP) channels in the substantia nigra pars compacta (SNc) promote Parkinson disease (PD) pathogenesis, thus blocking K-ATP channels may protect neurons against neuronal degeneration. In the present study, we tested a hypothesis that THB blocks K-ATP channels in dopaminergic (DA) neurons acutely dissociated from rat SNc. Using perforated patch-clamp recording in current-clamp mode, the functional K-ATP channels can be opened by persistent perfusion of rotenone, an inhibitor of complex I of the mitochondrial respiratory chain. Bath-application of THB reversibly blocks opened K-ATP channels in a concentration-dependent manner, which is comparable to a classical K-ATP channel blocker, Tol. Compared to THB analogs, l-stepholidine (l-SPD) or l-tetrahydropalmatine (l-THP), THB exhibits more profound blockade in K-ATP channels. In addition, exposure of THB alone to the recorded neuron increases action potential firing, and THB also restores rotenone-induced membrane hyperpolarization in the presence of dopamine D2 receptor antagonist (sulpiride), suggesting that THB exhibits an excitatory effect on SNc DA neurons through the block of K-ATP channels. Collectively, the blockade of neuronal K-ATP channels by THB in SNc DA neurons is a novel pharmacological mechanism of THB, which may contribute to its neuroprotective effects in PD. (C) 2010 Elsevier Ltd. All rights reserved.

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