Literature DB >> 8388192

GABAB receptor pharmacology.

N G Bowery1.   

Abstract

In conclusion, GABAB receptors appear to be of major importance in synaptic processing within the brain and are present at both post- and presynaptic sites. Their activation can hyperpolarize neurones and diminish neurotransmitter release from presynaptic terminals. We already know that drugs, i.e. baclofen, that mimic this activation are therapeutically useful, although the full significance of their use both inside and outside the brain has yet to be realized. Drugs that interfere with GABAB receptor activation should also prove to be important therapeutic agents. A number of suggestions have been proposed but it will be many years before the potential effects can be consolidated or refuted in humans. Only now are brain-penetrating GABAB antagonists being discovered, due largely to the expertise of the research group at CIBA-Geigy, Basel. The emergence of such compounds makes future studies an exciting prospect. In particular, the discovery that GABAB antagonism can suppress absence seizures in rats has provided an important therapeutic target. It is now just over ten years since we first designated the term GABAB. Since then a wealth of information has been obtained, but perhaps the best is still to come.

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Year:  1993        PMID: 8388192     DOI: 10.1146/annurev.pa.33.040193.000545

Source DB:  PubMed          Journal:  Annu Rev Pharmacol Toxicol        ISSN: 0362-1642            Impact factor:   13.820


  80 in total

1.  Heteromeric assembly of GABA(B)R1 and GABA(B)R2 receptor subunits inhibits Ca(2+) current in sympathetic neurons.

Authors:  A K Filippov; A Couve; M N Pangalos; F S Walsh; D A Brown; S J Moss
Journal:  J Neurosci       Date:  2000-04-15       Impact factor: 6.167

2.  The GABAB receptor interacts directly with the related transcription factors CREB2 and ATFx.

Authors:  J H White; R A McIllhinney; A Wise; F Ciruela; W Y Chan; P C Emson; A Billinton; F H Marshall
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

3.  GABA(B2) is essential for g-protein coupling of the GABA(B) receptor heterodimer.

Authors:  M J Robbins; A R Calver; A K Filippov; W D Hirst; R B Russell; M D Wood; S Nasir; A Couve; D A Brown; S J Moss; M N Pangalos
Journal:  J Neurosci       Date:  2001-10-15       Impact factor: 6.167

4.  GABA receptors modulate trigeminovascular nociceptive neurotransmission in the trigeminocervical complex.

Authors:  R J Storer; S Akerman; P J Goadsby
Journal:  Br J Pharmacol       Date:  2001-10       Impact factor: 8.739

5.  Pretreatment of rat brain synaptosomes with GABA increases subsequent GABA uptake via GABA(B) receptor activation.

Authors:  A Cupello; S Scarrone
Journal:  Neurochem Res       Date:  2001-01       Impact factor: 3.996

6.  The C-terminal domains of the GABA(b) receptor subunits mediate intracellular trafficking but are not required for receptor signaling.

Authors:  A R Calver; M J Robbins; C Cosio; S Q Rice; A J Babbs; W D Hirst; I Boyfield; M D Wood; R B Russell; G W Price; A Couve; S J Moss; M N Pangalos
Journal:  J Neurosci       Date:  2001-02-15       Impact factor: 6.167

Review 7.  CNS involvement in overactive bladder: pathophysiology and opportunities for pharmacological intervention.

Authors:  Karl-Erik Andersson; Rikard Pehrson
Journal:  Drugs       Date:  2003       Impact factor: 9.546

Review 8.  Ion channels and signaling in the pituitary gland.

Authors:  Stanko S Stojilkovic; Joël Tabak; Richard Bertram
Journal:  Endocr Rev       Date:  2010-07-21       Impact factor: 19.871

9.  Cationic modulation of rho 1-type gamma-aminobutyrate receptors expressed in Xenopus oocytes.

Authors:  D J Calvo; A E Vazquez; R Miledi
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-20       Impact factor: 11.205

10.  GABA, glutamate and substance P-like immunoreactivity release: effects of novel GABAB antagonists.

Authors:  H Teoh; M Malcangio; N G Bowery
Journal:  Br J Pharmacol       Date:  1996-07       Impact factor: 8.739

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