نتایج جستجو برای: ep1 subtype

تعداد نتایج: 55884  

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2012
Xianwu Li Eiron Cudaback Richard M Breyer Kathleen S Montine C Dirk Keene Thomas J Montine

A major therapeutic target for Parkinson's disease (PD) is providing increased glial-derived neurotrophic factor (GDNF) to dopaminergic neurons. We tested the hypothesis that innate immune activation increases astrocyte GDNF production and that this is regulated by specific eicosanoid receptors. Innate immune-activated primary murine astrocytes were assayed for GDNF expression and secretion. Co...

2011
Behnoush Zare Armin Madadkar-Sobhani Siavoush Dastmalchi Masoud Mahmoudian

The prostanoid receptor EP1 is a G-protein-coupled receptor (GPCR) known to be involved in a variety of pathological disorders such as pain, fever and inflammation. These receptors are important drug targets, but design of subtype specific agonists and antagonists has been partially hampered by the absence of three-dimensional structures for these receptors. To understand the molecular interact...

Journal: :Hypertension 2012
Christina S Bartlett Kelli L Boyd Raymond C Harris Roy Zent Richard M Breyer

Prostaglandin E(2) is a major prostanoid found in the kidney and vasculature contributing to the regulation of blood pressure. The prostaglandin E(2) receptor EP1 has been shown to contribute to hypertension by mediating angiotensin II-dependent vasoconstriction, although its precise role is incompletely characterized. Disruption of the EP1 receptor in C57BL/6J mice reduced the incidence of mor...

Journal: :Journal of physiology and pharmacology : an official journal of the Polish Physiological Society 2014
K Takeuchi

Endogenous prostaglandins (PGs) play a role in modulating mucosal integrity and have various functions in the stomach, with E type PGs being the most effective. PGE₂ provides gastric cytoprotection against damage induced in rats by HCl/ethanol, indomethacin, or acid back-diffusion after barrier disruption. These effects were mimicked by EP1 agonists and/or attenuated by an EP1 antagonist, and d...

2013
Shekher Mohan Alexander V. Glushakov Alexander deCurnou Shuh Narumiya Sylvain Doré

Although hemin-mediated neurotoxicity has been linked to the production of free radicals and glutamate excitotoxicity, the role of the prostaglandin E2 (PGE2)-EP1 receptor remains unclear. Activation of the EP1 receptor in neurons results in increased intracellular calcium levels; therefore, we hypothesize that the blockade of the EP1 receptor reduces hemin neurotoxicity. Using postnatal primar...

2013
Jae Yeoul Jun

CC This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons. org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. *Correspondence: Jae Yeoul Jun, MD, PhD Department of Physiology, Chosun Univesity Schoo...

2016
Jinshun Pan Qinyi Yang Jiaofang Shao Li Zhang Juan Ma Yipin Wang Bing-Hua Jiang Jing Leng Xiaoming Bai

Cyclooxygenase-2 (COX-2) has been implicated in cell invasion in non-small-cell lung cancer (NSCLC). However, the mechanism is unclear. The present study investigated the effect of COX-2 on β1-integrin expression and cell invasion in NSCLC. COX-2 and β1-integrin were co-expressed in NSCLC tissues. COX-2 overexpression or Prostaglandin E2 (PGE2) treatment increased β1-integrin expression in NSCL...

Journal: :The Journal of Experimental Medicine 2007
Miyako Nagamachi Daiji Sakata Kenji Kabashima Tomoyuki Furuyashiki Takahiko Murata Eri Segi-Nishida Kitipong Soontrapa Toshiyuki Matsuoka Yoshiki Miyachi Shuh Narumiya

Prostaglandin E2 (PGE2) exerts its actions via four subtypes of the PGE receptor, EP1-4. We show that mice deficient in EP1 exhibited significantly attenuated Th1 response in contact hypersensitivity induced by dinitrofluorobenzene (DNFB). This phenotype was recapitulated in wild-type mice by administration of an EP1-selective antagonist during the sensitization phase, and by adoptive transfer ...

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