تفاصيل الوثيقة

نوع الوثيقة : مقال في مجلة دورية 
عنوان الوثيقة :
An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors.
An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors.
 
لغة الوثيقة : الانجليزية 
المستخلص : Huang SM, Bisogno T, Trevisani M, Al-Hayani A, De Petrocellis L, Fezza F, Tognetto M, Petros TJ, Krey JF, Chu CJ, Miller JD, Davies SN, Geppetti P, Walker JM, Di Marzo V. Departments of Psychology and Neuroscience, Brown University, Providence, RI 02912, USA. The vanilloid receptor VR1 is a nonselective cation channel that is most abundant in peripheral sensory fibers but also is found in several brain nuclei. VR1 is gated by protons, heat, and the pungent ingredient of "hot" chili peppers, capsaicin. To date, no endogenous compound with potency at this receptor comparable to that of capsaicin has been identified. Here we examined the hypothesis, based on previous structure-activity relationship studies and the availability of biosynthetic precursors, that N-arachidonoyl-dopamine (NADA) is an endogenous "capsaicin-like" substance in mammalian nervous tissues. We found that NADA occurs in nervous tissues, with the highest concentrations being found in the striatum, hippocampus, and cerebellum and the lowest concentrations in the dorsal root ganglion. We also gained evidence for the existence of two possible routes for NADA biosynthesis and mechanisms for its inactivation in rat brain. NADA activates both human and rat VR1 overexpressed in human embryonic kidney (HEK)293 cells, with potency (EC(50) approximately 50 nM) and efficacy similar to those of capsaicin. Furthermore, NADA potently activates native vanilloid receptors in neurons from rat dorsal root ganglion and hippocampus, thereby inducing the release of substance P and calcitonin gene-related peptide (CGRP) from dorsal spinal cord slices and enhancing hippocampal paired-pulse depression, respectively. Intradermal NADA also induces VR1-mediated thermal hyperalgesia (EC(50) = 1.5 +/- 0.3 microg). Our data demonstrate the existence of a brain substance similar to capsaicin not only with respect to its chemical structure but also to its potency at VR1 receptors. PMID: 12060783 [PubMed - indexed for MEDLINE] 
ردمد : 12060783 
اسم الدورية : Proc Natl Acad Sci U S A 
المجلد : 99 
العدد : 12 
سنة النشر : 2002 هـ
2002 م
 
نوع المقالة : مقالة علمية 
تاريخ الاضافة على الموقع : Saturday, March 20, 2010 

الباحثون

اسم الباحث (عربي)اسم الباحث (انجليزي)نوع الباحثالمرتبة العلميةالبريد الالكتروني
عبدالمنعم اللحيانيAl-Hayani, Abdel-Moneim باحثدكتوراه 

الملفات

اسم الملفالنوعالوصف
 26076.doc doc 

الرجوع إلى صفحة الأبحاث