Download e-book for iPad: A3 Adenosine Receptors from Cell Biology to Pharmacology and by John R. Fozard (auth.), Pier Andrea Borea (eds.)

By John R. Fozard (auth.), Pier Andrea Borea (eds.)

ISBN-10: 904813143X

ISBN-13: 9789048131433

ISBN-10: 9048131448

ISBN-13: 9789048131440

This publication "A3 Adenosine Receptors from telephone Biology to Pharmacology and Therapeutics " records the current country of data of the adenosine A3 receptor. Adenosine A3 receptors are G protein-linked receptors that functionality in body structure and intracellular signaling and are fascinated by inflammatory responses and mediating phone proliferation and mobilephone loss of life.

The A3 receptor is more and more being well-known for its organic roles during the physique, and lots of A3 receptor ligands have confirmed important in elucidating peripheral and valuable pathologies. This ebook covers a variety of details together with info from reviews of theoretical, molecular and mobile pharmacology, sign transduction, integrative body structure, new drug discoveries and medical functions. The booklet contains sections on:

  • A3 Adenosine Receptor sign transduction
  • Adenosine Receptor medicinal chemistry
  • Effects and healing functions of Adenosine Receptors on tissues and organs
  • Adenosine Receptors and inflammatory and auto-immune diseases
  • Adenosine Receptors and cancer

The chapters during this booklet hide either basic technological know-how and correct purposes and supply an authoritative account of the present prestige of the sphere. "A3 Adenosine Receptors from cellphone Biology to Pharmacology and Therapeutics" is an up to the moment and scientifically first-class resource of knowledge, appealing to easy and scientific scientists alike.

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Additional info for A3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics

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3 mg kg−1; filled columns) or saline (open columns). Responses are expressed relative to the response to bethanechol (100 mM) which was taken as 100%. Mean values (± SEM) from the number of individual experiments shown in parentheses are presented. R. 1 + 1 (6) Cl-IB-MECA Methysergide Cl-IB-MECA DPCPX Cl-IB-MECA + + + Methysergide Methysergide DPCPX Fig. 3 mg kg−1 intratracheally). Responses are expressed relative to the response to bethanechol (100 mM) which was taken as 100%. Mean values (±SEM) from the number of individual experiments shown in parentheses are presented.

The interaction led me through basic and applied pharmacology and resulted in a fascinating insight into one small part of the biological significance of this receptor. My chemistry colleagues discovered impressive molecules with the potential for use as pharmacological tools and, in the case of QAF805, for a Proof of Mechanism clinical evaluation. As is usual in these situations, there remain a number of unanswered questions which will have to be explored by others. For instance, time ran out before I could test for antagonist activity of 2-Cl-IBMECA against adenosine in vivo.

Br J Pharmacol 145:1009–1015 Hughes PJ, Holgate ST, Church MK (1984) Adenosine inhibits and potentiates IgE-dependent histamine release from human lung mast cells by an A2-purinoceptor mediated mechanism. Biochem Pharmacol 33:3847–3852 Jacobson KA, Gao Z-G (2006) Adenosine receptors as therapeutic targets. Nat Rev Drug Discov 5:247–264 Jacobson KA, Nikodijevic D, Shi D, Gallo-Rodriguez C, Olah ME, Stiles G, Daly JW (1993) A role for central A3-adenosine receptors: mediation of central depressant effects.

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A3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics by John R. Fozard (auth.), Pier Andrea Borea (eds.)


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