کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5823484 | 1118332 | 2014 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Probing biased/partial agonism at the G protein-coupled A2B adenosine receptor
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کلمات کلیدی
GPCRR-PIAKrebs Ringer bicarbonate bufferCyclic AMP (cAMP)IB-MECAKRBBNECACPCACGS21680DMEMCPAHEPESGAPDHPurinesHEKERK2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid - 2- [4- (2-hydroxyethyl) piperazin-1-yl] ethanesulfonic acidcyclic AMP - AMP cyclicDulbecco's modified Eagle's medium - Medal of Eagle اصلاح شده DulbeccoN6-cyclopentyladenosine - N6-سیکلوپنتیلادنوزینArrestin - آرستینCho - برایChinese Hamster Ovary - تخمدان هامستر چینیCalcium - کلسیمhuman embryonic kidney - کلیه جنین انسانextracellular-signal-regulated kinase - کیناز تنظیم شده خارج سلولی سیگنالglyceraldehyde 3-phosphate dehydrogenase - گلیسرولیدید 3-فسفات دهیدروژنازAdenosine receptor - گیرنده آدنوزینG protein-coupled receptor - گیرندههای جفتشونده با پروتئین جی
موضوعات مرتبط
علوم پزشکی و سلامت
داروسازی، سم شناسی و علوم دارویی
داروشناسی
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Probing biased/partial agonism at the G protein-coupled A2B adenosine receptor Probing biased/partial agonism at the G protein-coupled A2B adenosine receptor](/preview/png/5823484.png)
چکیده انگلیسی
G protein-coupled A2B adenosine receptor (AR) regulates numerous important physiological functions, but its activation by diverse A2BAR agonists is poorly profiled. We probed potential partial and/or biased agonism in cell lines expressing variable levels of endogenous or recombinant A2BAR. In cAMP accumulation assays, both 5â²-substituted NECA and C2-substituted MRS3997 are full agonists. However, only 5â²-substituted adenosine analogs are full agonists in calcium mobilization, ERK1/2 phosphorylation and β-arrestin translocation. A2BAR overexpression in HEK293 cells markedly increased the agonist potency and maximum effect in cAMP accumulation, but less in calcium and ERK1/2. A2BAR siRNA silencing was more effective in reducing the maximum cAMP effect of non-nucleoside agonist BAY60-6583 than NECA's. A quantitative 'operational model' characterized C2-substituted MRS3997 as either balanced (cAMP accumulation, ERK1/2) or strongly biased agonist (against calcium, β-arrestin). N6-substitution biased against ERK1/2 (weakly) and calcium and β-arrestin (strongly) pathways. BAY60-6583 is ERK1/2-biased, suggesting a mechanism distinct from adenosine derivatives. BAY60-6583, as A2BAR antagonist in MIN-6 mouse pancreatic β cells expressing low A2BAR levels, induced insulin release. This is the first relatively systematic study of structure-efficacy relationships of this emerging drug target.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical Pharmacology - Volume 90, Issue 3, 1 August 2014, Pages 297-306
Journal: Biochemical Pharmacology - Volume 90, Issue 3, 1 August 2014, Pages 297-306
نویسندگان
Zhan-Guo Gao, Ramachandran Balasubramanian, Evgeny Kiselev, Qiang Wei, Kenneth A. Jacobson,