Literature DB >> 3343292

Effects of nifedipine and felodipine on adenosine and inosine release from the hypoxemic rat cerebral cortex.

J W Phillis1, M H O'Regan, G A Walter.   

Abstract

The cerebral cortical cup technique has been used to study the effects of nifedipine and felodipine on adenosine and inosine release from the rat brain. After basal and hypoxia (8% 02)-evoked control levels of purine release had been established, these 1,4-dihydropyridine calcium antagonists were administered intraperitoneally (1 mg/kg). Both agents depressed basal levels of purine efflux and suppressed the hypoxia-evoked release of adenosine and inosine. An inhibition of the transporter that mediates purine efflux from brain cells is likely to account for the suppression of release from the cerebral cortex. A reduced release of adenosine into the interstitial space also explains the ability of both agents to block the increase in CBF evoked by hypoxic challenges.

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Year:  1988        PMID: 3343292     DOI: 10.1038/jcbfm.1988.47

Source DB:  PubMed          Journal:  J Cereb Blood Flow Metab        ISSN: 0271-678X            Impact factor:   6.200


  4 in total

1.  Nimodipine and nifedipine enhance transmission at the Schaffer collateral CA1 pyramidal neuron synapse.

Authors:  M H O'Regan; J D Kocsis; S G Waxman
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

2.  The adenosine metabolite inosine is a functional agonist of the adenosine A2A receptor with a unique signaling bias.

Authors:  Ajith A Welihinda; Manmeet Kaur; Kelly Greene; Yongjiao Zhai; Edward P Amento
Journal:  Cell Signal       Date:  2016-02-19       Impact factor: 4.315

3.  Enhancement of inosine-mediated A2AR signaling through positive allosteric modulation.

Authors:  Ajith A Welihinda; Manmeet Kaur; Kaviya S Raveendran; Edward P Amento
Journal:  Cell Signal       Date:  2017-11-08       Impact factor: 4.315

4.  Effect of oral nimodipine on cerebral infarction and outcome after subarachnoid haemorrhage: British aneurysm nimodipine trial.

Authors:  J D Pickard; G D Murray; R Illingworth; M D Shaw; G M Teasdale; P M Foy; P R Humphrey; D A Lang; R Nelson; P Richards
Journal:  BMJ       Date:  1989-03-11
  4 in total

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