کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9001743 | 1118549 | 2005 | 14 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Contrasting the effects of nifedipine on subtypes of endogenous and recombinant T-type Ca2+ channels
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کلمات کلیدی
IC50LVAAmaxThalamic neuronsDMSO - DMSOI–V - I - VV1/2 - V1 / 2laterodorsal - بعد از زایمانXenopus oocytes - تخمک XenopusDimethyl sulfoxide - دیمتیل سولفواکسیدcurrent–voltage relationship - رابطه جریان ولتاژslope factor - فاکتور شیبNifedipine - نیفدیپینhalf-inhibitory concentration - نیمه مهار کننده غلظتhigh voltage-activated - ولتاژ بالا فعال می شودlow voltage-activated - ولتاژ پایین فعال شده استMembrane potential - پتانسیل غشاء HVA - چه
موضوعات مرتبط
علوم پزشکی و سلامت
داروسازی، سم شناسی و علوم دارویی
داروشناسی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
There is evidence that nifedipine (Nif) - a dihydropyridine (DHP) Ca2+-channel antagonist mostly known for its L-type-specific action - is capable of blocking low voltage-activated (LVA or T-type) Ca2+ channels as well. However, the discrimination by Nif of either various endogenous T-channel subtypes, evident from functional studies, or cloned Cav3.1, Cav3.2 and Cav3.3 T-channel α1 subunits have not been determined. Here, we investigated the effects of Nif on currents induced by Cav3.1, Cav3.2 and Cav3.3 expression in Xenopus oocytes or HEK-293 cells (Iα1G, Iα1H and Iα1I, respectively) and two kinetically distinct, “fast” and “slow”, LVA currents in thalamic neurons (ILVA,f and ILVA,s). At voltages of the maximums of respective currents the drug most potently blocked Iα1H (IC50 = 5 μM, max block 41%) followed by Iα1G (IC50 = 109 μM, 23%) and Iα1I (IC50 = 243 μM, 47%). The mechanism of blockade included interaction with Cav3.1, Cav3.2 and Cav3.3 open and inactivated states. Nif blocked thalamic ILVA,f and ILVA,s with nearly equal potency (IC50 = 22 μM and 28 μM, respectively), but with different maximal inhibition (81% and 51%, respectively). We conclude that Cav3.2 is the most sensitive to Nif, and that quantitative characteristics of drug action on T-type Ca2+ channels depend on cellular system they are expressed in. Some common features in the voltage- and state-dependence of Nif action on endogenous and recombinant currents together with previous data on T-channel α1 subunits mRNA expression patterns in the thalamus point to Cav3.1 and Cav3.3 as the major contributors to thalamic ILVA,f and ILVA,s, respectively.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical Pharmacology - Volume 69, Issue 5, 1 March 2005, Pages 841-854
Journal: Biochemical Pharmacology - Volume 69, Issue 5, 1 March 2005, Pages 841-854
نویسندگان
Alexander Shcheglovitov, Tatiana Zhelay, Yulia Vitko, Vadim Osipenko, Edward Perez-Reyes, Platon Kostyuk, Yaroslav Shuba,