نتایج جستجو برای: گیرنده nmda

تعداد نتایج: 21720  

Introduction: In the present work, spontaneous postsynaptic currents were assessed to investigate the postnatal development of excitatory postsynaptic currents in locus coeruleus neurons. Methods: In this study, AMPA and NMDA receptor-mediated spontaneous synaptic currents in the neurons of locus coeruleus were assessed using whole cell voltage-clamp recording during the first three weeks. ...

ژورنال: :مجله دانشگاه علوم پزشکی مازندران 0
داوود فرزین d farzin متخصص فارماکولوژی- استادیار دانشگاه علوم پزشکی مازندران خاطره سورتجی kh soorteje

سابقه و هدف: دکسترومتورفان یک آنتاگونیست غیر رقابتی گیرنده nmda گلوتامات می باشد که به عنوان یک داروی ضدسرفه otc مورد استفاده قرار می گیرد. در مطالعه قبلی خود که نتایج آن در مجلهeur. j. pharmacol., 1999, 377, 35-42 چاپ شده است نشان داده ام که دکسترومتورفان از طریق مسیرهای اوپیوییدی و دوپامینرژیک قادر است علایم سندرم withdrawal القا شده توسط نالوکسون در موش های وابسته به مرفین را تقلیل دهد. مطال...

Abdolrasool Khalafi, Ali Mostafaie, Ali Pourmotabbed, Hedayat Sahraei, Reza Hajihosseini, Seyed Ershad Nedaei,

Introduction: N-methyl-D-aspartate (NMDA) receptors play a pivotal role in the development of tolerance and physical dependence to opiates. Activation of NMDA receptors involves the induction of long term potentiation (LTP) in hippocampus. Our previous study suggested that chronic oral administration of morphine enhanced NMDA dependent LTP in the CA1 area of hippocampal slices of rats. The p...

Journal: :Indian journal of forensic medicine and toxicology 2021

A single Memory impairment substantially reduces the quality of life in elderly. It is associated with thealteration neurotrophic (NT) factors, such as brain-derived factor (BDNF) and glutamatereceptor N-methyl-D-aspartate (NMDA). Exercise often used to reduce cognitive impairment. Previousstudies show that benefits aerobic exercises on impairments are correlated increasing BDNFand preventing p...

Journal: :anesthesiology and pain medicine 0
manzumeh-shamsi meymandi neuroscience research center, institute of neuropharmacology, kerman university of medical sciences, kerman, iran fariborz keyhanfar pharmacology department, iran university of medical sciences, tehran, iran; pharmacology department, iran university of medical sciences, tehran, iran. tel: +98-2188058696, fax: +98-2188052978 omid yazdanpanah neuroscience research center, institute of neuropharmacology, kerman university of medical sciences, kerman, iran gioia heravi neuroscience research center, institute of neuropharmacology, kerman university of medical sciences, kerman, iran

conclusions our findings support the role of nmdars in pregabalin antinociception, because the nmdar agonist, unlike the antagonist, decreased the antinociceptive effect of pregabalin, even if tail flick is not an adequate pain assessment method in this regard. background pregabalin as a new anticonvulsant has been used in different pain treatments. objectives the aim of this study was to inves...

Journal: :iranian journal of pharmaceutical research 0
mehdi saberi baqiyatallah university of medical sciences, dept. of pharmacology and toxicology fatemeh saberi tehran university of medical sciences roshanak vesali tehran university

although the epileptogenic properties of estrogens have been widely demonstrated in several models and species, the mechanism(s) by which estrogens can acutely change seizure parameters including after discharge and seizure duration remain remains to be determined. in the present study, we examined the role of nmda (n-methyl-d-aspartate), non-nmda and estrogenic receptors in estradiol benzoate ...

Journal: :مجله علوم اعصاب شفای خاتم 0
ali jahanbazi jahan-abad shefa neuroscience research center, khatam alanbia hospital tehran, iran

long-term potentiation (ltp) is a reflection of synaptic plasticity that induced by specific patterns of synaptic activity and has an important role in learning and memory. the first clue of the potential role of glutamate receptors in ltp was in 1991 with the observation that the mglur agonists 1-amino-1, 3-cyclopentanedicarboxylic acid (acpd), increased ltp. studies have shown that acpd induc...

Journal: :مجله علوم اعصاب شفای خاتم 0
milad ahmadi a. shefa neuroscience research center, khatam alanbia hospital, tehran, iran. b. faculty of veterinary medicine, islamic azad university, karaj branch, karaj, iran. azadeh sajadian shefa neuroscience research center, khatam alanbia hospital, tehran, iran. hadi aligholi a. shefa neuroscience research center, khatam alanbia hospital, tehran, iran. b. department of neurosciences, school of advanced technologies in medicine, tehran university of medical sciences, tehran, iran. babak khodaie shefa neuroscience research center, khatam alanbia hospital, tehran, iran. ahmad ali lotfinia shefa neuroscience research center, khatam alanbia hospital, tehran, iran. mahmoud lotfinia a. shefa neuroscience research center, khatam alanbia hospital, tehran, iran. b. shahid beheshti university of medical sciences, tehran, iran.

the n-methyl-d-aspartic acid (nmda) receptor is one of the specific types of ionotropic receptors which lied to glutaminergic system. it has been widely accepted that nmda receptor neurons promote anxiety, in humans as well as in animal models. however, in the previous study seems inhibiting of this receptors decreased the protective role in neural cell. demonstration of nmda receptor activity ...

Journal: :physiology and pharmacology 0
roghaieh khakpay department of animal science, faculty of natural sciences, university of tabriz, tabriz, iran maryam azaddar department of animal science, faculty of natural sciences, university of tabriz, tabriz, iran fatemeh khakpay institute for cognitive science studies (icss), tehran, iran

introduction: the nucleus paragigantocellularis lateralis (lpgi) is involved in the descending pain modulation. the neurostreoid, 17β-estradiol found in the pgi nucleus and modulates nociception by binding to estrogen receptors and also by allosteric interaction with nmda receptors. in this study, the role of nmda receptors in the 17β-estradiol-induced pain modulation was investigated by assess...

ژورنال: :مجله دانشگاه علوم پزشکی مازندران 0
داوود فرزین d farzin دکترای فارماکولوژی، عضو هیأت علمی (دانشیار) دانشکده پزشکی و مرکز تحقیقات روان پزشکی و علوم و فناوری دانشگاه علوم پزشکی مازندران مهتا مهرابیان m mehrabian

سابقه و هدف: دکسترومتورفان آنتاگونیست غیر رقابتی گیرنده nmda سیستم گلوتامات- ارژیک می باشد که به عنوان یک داروی ضدسرفهotc ، بیش از 47 سال کاربرد بالینی دارد. نظر به این که اثر و مکانیسم های اوپیوییدی و دوپامینرژیک دکسترومتورفان در مدل های فازیک و حاد درد بررسی نشده است، در این مطالعه اثر دکسترومتورفان بر پاسخ درد ناشی از صفحه داغ در موش مورد آزمایش قرار گرفت.مواد و روش ها: اثر دکستــرومتــورفان...

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