Literature DB >> 1316981

Recent developments in the classification and functional significance of receptors for ATP and UTP, evidence for nucleotide receptors.

S E O'Connor1.   

Abstract

The presence of a nucleotide receptor activated with similar potencies by UTP and ATP is suggested by recent data from a variety of different cell types. This receptor type appears distinct from previously described ATP-sensitive P2-purinoceptor subtypes and, probably, from other UTP-sensitive receptors, however further studies using selective antagonists are necessary to provide a definitive characterisation. Although the functional role of endogenous extracellular ATP has already achieved recognition there are also many diverse examples of cells and tissues which respond to UTP at micromolar or sub-micromolar concentrations. Therefore, the possible physiological importance of UTP is a fertile area for further investigation. The functional significance of ATP/UTP receptors is underlined by recent demonstrations that UTP and ATP modulate chloride ion secretion in human airways epithelium, possibly by activation of a nucleotide receptor, an effect which may have potential clinical utility in the treatment of cystic fibrosis.

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Year:  1992        PMID: 1316981     DOI: 10.1016/0024-3205(92)90420-t

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  26 in total

1.  Co-existence of P2Y-and PPADS-insensitive P2U-purinoceptors in endothelial cells from adrenal medulla.

Authors:  J Mateo; M T Miras-Portugal; E Castro
Journal:  Br J Pharmacol       Date:  1996-11       Impact factor: 8.739

2.  Responses of the longitudinal muscle and the muscularis mucosae of the rat duodenum to adenine and uracil nucleotides.

Authors:  C R Johnson; S J Charlton; S M Hourani
Journal:  Br J Pharmacol       Date:  1996-03       Impact factor: 8.739

3.  The effects of purine compounds on the isolated aorta of the frog Rana temporaria.

Authors:  G E Knight; G Burnstock
Journal:  Br J Pharmacol       Date:  1996-03       Impact factor: 8.739

4.  Dissociation of P2 purinoceptor-mediated increase in intracellular Ca2+ level from myosin light chain phosphorylation and contraction in rat aorta.

Authors:  S Kitajima; K Harada; M Hori; H Ozaki; H Karaki
Journal:  Br J Pharmacol       Date:  1996-06       Impact factor: 8.739

5.  Suramin analogs, divalent cations and ATP gamma S as inhibitors of ecto-ATPase.

Authors:  M W Beukers; C J Kerkhof; M A van Rhee; U Ardanuy; C Gurgel; H Widjaja; P Nickel; A P IJzerman; W Soudijn
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1995-05       Impact factor: 3.000

6.  Increases in intracellular calcium via activation of an endogenous P2-purinoceptor in cultured CHO-K1 cells.

Authors:  P A Iredale; S J Hill
Journal:  Br J Pharmacol       Date:  1993-12       Impact factor: 8.739

7.  Effect of tienoxolol, a new diuretic beta-blocking agent, on urinary prostaglandin excretion in the rat.

Authors:  F Caussade; A Cloarec
Journal:  Br J Pharmacol       Date:  1993-05       Impact factor: 8.739

8.  Responses of the aorta of the garter snake (Thamnophis sirtalis parietalis) to purines.

Authors:  G E Knight; G Burnstock
Journal:  Br J Pharmacol       Date:  1995-01       Impact factor: 8.739

9.  The effects of ATP and alpha,beta-methylene-ATP on cytosolic Ca2+ level and force in rat isolated aorta.

Authors:  S Kitajima; H Ozaki; H Karaki
Journal:  Br J Pharmacol       Date:  1993-09       Impact factor: 8.739

10.  Activation of nucleotide receptors inhibits M-type K current [IK(M)] in neuroblastoma x glioma hybrid cells.

Authors:  A K Filippov; A A Selyanko; J Robbins; D A Brown
Journal:  Pflugers Arch       Date:  1994-12       Impact factor: 3.657

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