کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2561603 | 1126942 | 2006 | 11 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Properties of voltage-gated Na+ channels in the human rhabdomyosarcoma cell-line SJ-RH30: Conventional and automated patch clamp analysis
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
HEPESEGTAS.E.M.TTXCell-line4-(2-hydroxyethyl)-1-piperazineethanesulphonic acid - 4- (2-hydroxyethyl) -1-piperazineethanesulphonic acidI–V - I - VEDTA - اتیلن دی آمین تترا استیک اسید Ethylenediaminetetraacetic acid - اتیلینیدامین تتراستیک اسیدElectrophysiology - الکتروفیزیولوژیtetrodotoxin - تترو دوتوکسین standard error of the mean - خطای استاندارد میانگینSkeletal muscle - عضله اسکلتیSodium Channel - کانال سدیمIon channel - کانال یونی
موضوعات مرتبط
علوم پزشکی و سلامت
داروسازی، سم شناسی و علوم دارویی
داروشناسی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Conventional and automated patch clamp electrophysiology were used to characterise the Na+ current of the SJ-RH30 human rhabdomyosarcoma. In conventional recordings SJ-RH30 cells exhibited a fast activating, fast inactivating Na+ current at potentials positive to â40 mV; in full current-voltage curves maximum current occurred between â20 and â10 mV. Inactivation kinetics at 0 mV were biexponential with time constants of 0.5 and 3.7 ms. Deinactivation at â90 mV also exhibited two kinetic components. Tetrodotoxin (TTX) blocked the Na+ current completely at 1 μM. The NaV 1.4 selective toxin μ-CTx-GIIIB reversibly blocked the Na+ current â¼60% at 10 μM. Very similar biophysical behaviour was observed in automated patch clamp and conventional recordings. For example, inactivation mid-point was â72 ± 2 mV (slope factor 7.2 ± 0.2) in automated patch clamp and â74 ± 2 mV (slope factor 7.4 ± 0.4) with conventional recording. The corresponding values for activation mid-point were â33.2 ± 2.4 and â30.3 ± 2.7 mV (slope 5.8 ± 0.3 and 6.4 ± 0.3, respectively). The throughput of the automated method was used to generate additional pharmacological data on inhibition of the Na+ current. TTX inhibited with an IC50 of 23 nM. μ-CTx-GIIIB also inhibited the channel in a concentration-dependent manner. Inhibition produced by both tetracaine and amitriptyline were shown to be frequency-dependent. Our experiments indicate that the Na+ current of SJ-RH30 cells arises mainly from channels with a phenotype like recombinant NaV 1.4 channels. The suitability of these cells for automated patch clamp suggests they may be useful for higher throughput studies of the interaction of drugs with human skeletal muscle Na+ channels.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Pharmacological Research - Volume 54, Issue 2, August 2006, Pages 118-128
Journal: Pharmacological Research - Volume 54, Issue 2, August 2006, Pages 118-128
نویسندگان
Andrew Randall, Nicolle McNaughton, Paula Green,