PSB 603 – a known selective adenosine A2B receptor antagonist – has anti-inflammatory activity in mice
نویسندگان
چکیده
A2B adenosine receptors are present in a wide spectrum of tissues, especially on cells the immune system. Since these particular have lowest, all receptor subtypes, affinity for they believed to play special role immunological processes associated with elevated levels such as inflammation. The aim this preliminary study was determine potential anti-inflammatory properties compound PSB-603, potent and selective antagonist, two different experimental models local systemic In model inflammation induced by carrageenan administration paw edema measured using pletysmometer. Additionally, C-reactive protein (CRP), interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-?) reactive oxygen species (ROS) were determined inflamed paw. Using mouse peripheral intraperitoneal (ip) zymosan A, influence antagonist infiltration neutrophils into peritoneum its effect plasma CRP, TNF-?, IL-6 investigated. results showed that PSB-603 administered at dose 5 mg/kg b.w. ip significantly reduced both tested models. Particularly, it decreased inflammatory cytokines IL-6, TNF-? ROS decreasing leukocytes. latter model, no statistically significant difference observed CRP level between control group without which has been treated compound. Thus, may indicate activity antagonists
منابع مشابه
Potent anti-inflammatory and antinociceptive activity of the endothelin receptor antagonist bosentan in monoarthritic mice
INTRODUCTION Endothelins are involved in tissue inflammation, pain, edema and cell migration. Our genome-wide microarray analysis revealed that endothelin-1 (ET-1) and endothelin-2 (ET-2) showed a marked up-regulation in dorsal root ganglia during the acute phase of arthritis. We therefore examined the effects of endothelin receptor antagonists on the development of arthritis and inflammatory p...
متن کاملEnhanced airway inflammation and remodeling in adenosine deaminase-deficient mice lacking the A2B adenosine receptor.
Adenosine is a signaling nucleoside that is generated in response to cellular injury and orchestrates the balance between tissue protection and the progression to pathological tissue remodeling. Adenosine deaminase (ADA)-deficient mice develop progressive airway inflammation and remodeling in association with adenosine elevations, suggesting that adenosine can promote features of chronic lung d...
متن کاملA2B Adenosine Receptor and Diabetic Erectile Dysfunction
141 Received June 1, 2015; revised and accepted September 4, 2015. Published online October 7, 2015; doi: 10.1620/tjem.237.141. Correspondence: Bohan Wang, M.D., Ph.D., Department of Urology, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Jiefang Road 88, Hangzhou 310009, China. e-mail: [email protected] A2B Adenosine Receptor Agonist Improves Erectile Function in Di...
متن کاملA2b adenosine receptor regulates hyperlipidemia and atherosclerosis.
BACKGROUND The cAMP-elevating A(2b) adenosine receptor (A(2b)AR) controls inflammation via its expression in bone marrow cells. METHODS AND RESULTS Atherosclerosis induced by a high-fat diet in apolipoprotein E-deficient mice was more pronounced in the absence of the A(2b)AR. Bone marrow transplantation experiments indicated that A(2b)AR bone marrow cell signals alone were not sufficient to e...
متن کاملA potent and selective histamine H4 receptor antagonist with anti-inflammatory properties.
Histamine mediates its physiological function through binding to four known histamine receptors. Here, we describe the first selective antagonist of the histamine H4 receptor, the newest member of the histamine receptor family, and provide evidence that such antagonists have anti-inflammatory activity in vivo. 1-[(5-chloro-1H-indol-2-yl)carbonyl]-4-methylpiperazine (JNJ 7777120) has a K(i) of 4...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Biomedicine & Pharmacotherapy
سال: 2021
ISSN: ['0753-3322', '1950-6007']
DOI: https://doi.org/10.1016/j.biopha.2020.111164