نتایج جستجو برای: ep2 subtype

تعداد نتایج: 56071  

2011
Sen Zhu Rui Xue Pan Zhao Fen-Ling Fan Xiaomu Kong Senfeng Zheng Qifei Han Yi Zhu Nanping Wang Jichun Yang Youfei Guan

Objective—Restenosis after angioplasty remains a major clinical problem. Prostaglandin E 2 (PGE 2) plays an important role in vascular homeostasis. The PGE 2 receptor E-prostanoid 2 (EP2) is involved in the proliferation and migration of various cell types. We aimed to determine the role of EP2 in the pathogenesis of neointimal formation after vascular injury. Methods and Results—Wire-mediated ...

2017
Miriam Peinhaupt Eva M. Sturm Akos Heinemann

Of the known prostanoid receptors, human eosinophils express the prostaglandin D2 (PGD2) receptors DP1 [also D-type prostanoid (DP)] and DP2 (also chemoattractant receptor homologous molecule, expressed on Th2 cells), the prostaglandin E2 receptors EP2 and EP4, and the prostacyclin (PGI2) receptor IP. Prostanoids can bind to either one or multiple receptors, characteristically have a short half...

2017
Erin Greaves Andrew W. Horne Helen Jerina Marta Mikolajczak Lisa Hilferty Rory Mitchell Sue M. Fleetwood-Walker Philippa T. K. Saunders

Endometriosis is an incurable gynecological disorder characterized by debilitating pain and the establishment of innervated endometriosis lesions outside the uterus. In a preclinical mouse model of endometriosis we demonstrated overexpression of the PGE2-signaling pathway (including COX-2, EP2, EP4) in endometriosis lesions, dorsal root ganglia (DRG), spinal cord, thalamus and forebrain. TRPV1,...

2015
Jing Wang Chun Li Yuan Cao Qiyan Wang Linghui Lu Hong Chang Yan Wu Jing Han Wei Wang Pengfei Tu Yong Wang

BACKGROUND Qi-shen-yi-qi (QSYQ), one of the most well-known traditional Chinese medicine (TCM) formulas, has been shown to have cardioprotective effects in rats with heart failure (HF) induced by acute myocardial infarction (AMI). However, the mechanisms of its therapeutic effects remain unclear. In this study, we aim to explore the mechanisms of QSYQ in preventing left ventricular remodelling ...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2008
Raymond E Hulse Wade G Swenson Phillip E Kunkler David M White Richard P Kraig

In brain, monomeric immunoglobin G (IgG) is regarded as quiescent and only poised to initiate potentially injurious inflammatory reactions via immune complex formation associated with phagocytosis and tumor necrosis factor alpha (TNF-alpha) production in response to disease. Using rat hippocampal slice and microglial cultures, here we show instead that physiological levels (i.e., 0.2-20 microg/...

2015
Yujiao Fu Myung-Soon Yang Jianxiong Jiang Thota Ganesh Eunhye Joe Raymond Dingledine

The timely resolution of inflammation prevents continued tissue damage after an initial insult. In the brain the death of activated microglia by apoptosis has been proposed as one mechanism to resolve brain inflammation. How microglia death is regulated after activation is still unclear. We reported that exposure to lipopolysaccharide (LPS) and interleukin-13 (IL-13) together initially activate...

Journal: :Endocrinology 2004
J A Arosh S K Banu S Kimmins P Chapdelaine L A Maclaren M A Fortier

Recognition and establishment of pregnancy involve several molecular and cellular interactions among the conceptus, uterus, and corpus luteum (CL). In ruminants, interferon-tau (IFNtau) of embryonic origin is recognized as the pregnancy recognition signal. Endometrial prostaglandin F(2alpha) (PGF(2alpha)) is the luteolysin, whereas PGE(2) is considered a luteoprotective or luteotrophic mediator...

Journal: :Biochemical pharmacology 2012
Brendan J Whittle Adam M Silverstein David M Mottola Lucie H Clapp

The prostacyclin analogues, iloprost and treprostinil are extensively used in treating pulmonary hypertension. Their binding profile and corresponding biochemical cellular responses on human prostanoid receptors expressed in cell lines, have now been compared. Iloprost had high binding affinity for EP1 and IP receptors (Ki 1.1 and 3.9 nM, respectively), low affinity for FP, EP3 or EP4 receptors...

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