کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2010421 1066973 2016 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Cyclosporine-A, but not tacrolimus significantly increases reactivity of vascular smooth muscle cells
ترجمه فارسی عنوان
سیکلوسپورین A _ اما نه تاکرولیموس _ واکنش پذیری سلول های عضلات صاف عروق را بطور چشمگیری افزایش می دهد
کلمات کلیدی
arg وازوپرسین. CSA، سیکلوسپورین A ؛ اثر تحریک دارویی؛ اثر حداکثر، محاسبه به عنوان یک درصد از پاسخ حداکثر برای کنترل؛ فنیل افرین؛ قدرت نسبی؛ محاسبه ED50 به عنوان ED50/کنترل
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
چکیده انگلیسی

BackgroundApplication of cyclosporine-A (CsA) or tacrolimus is associated with numerous side effects. One of the main reasons for restricting usage of CsA is hypertension. In tacrolimus treated subjects the frequency of these phenomena is significantly lower.The known molecular mechanism of action of tacrolimus and cyclosporine-A seems to be the same, thus we decided to compare modulatory effect of drugs on vascular smooth muscle contractility.MethodsExperiments were performed on isolated and perfused tail artery of Wistar rats. Contraction force was measured by increased degree of perfusion pressure with a constant flow rate.ResultsConcentration–response curves for agonist in the presence CsA were significantly shifted to the left with increase in maximal responses. This effect was due to increased calcium influx from extracellular calcium stores whereas there were no significant changes in calcium influx in the presence of tacrolimus; concentration–response curve was comparable to controls.ConclusionOur results strongly support the idea that main difference between effects on smooth muscle contractility of calcineurin-dependent immunosuppressants: CsA and tacrolimus is related to the different level of extracellular calcium influx to the cytoplasm. The elucidation of these mechanisms may permit the identification of new therapeutic strategies against CsA-induced hypertension.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Pharmacological Reports - Volume 68, Issue 1, February 2016, Pages 201–205
نویسندگان
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