Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Judith M. Hills"'
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:515-518
The GABAB receptor affinity of a number of GABA analogues, where the carboxylic acid group has been replaced with a range of acidic moieties, were determined. The phosphinic acid analogue (1) was identified as a potent selective GABAB ligand which is
Publikováno v:
ChemInform. 23
Autor:
Judith M. Hills, Philip I. Aaronson
Publikováno v:
Gastroenterology. 101:55-65
An investigation of the mechanism of peppermint oil action was performed using isolated pharmacological preparations from guinea pig large intestine and patch clamp electrophysiology techniques on rabbit jejunum. Peppermint oil relaxed carbachol-cont
Autor:
Kenneth B. Mackay, Frank C. Barone, Barry Sidney Orlek, Judith M. Hills, V.Ann Lewis, Andrew A. Parsons, Christopher D. Benham, Sarah J. Hadingham, A. Jacqueline Hunter, Colin A. Campbell, Raymond F. White, Mark H Harries, John David Harling
Publikováno v:
European journal of pharmacology. 401(3)
For progression to clinical trials in stroke, putative neuroprotective compounds should show robust efficacy post-ischaemia in several experimental models of stroke. This paper describes the characterisation of (+)(1S, 2R)-cis-1-[4-(1-methyl-1-phenyl
Publikováno v:
British journal of pharmacology. 102(3)
1. A series of GABAB receptor antagonists were tested against (+/-)-baclofen for activity on the presynaptic GABAB receptor in the rat vas deferens. 2. All the antagonists tested caused a rightward shift in the concentration-response curve to (+/-)-b
Publikováno v:
British journal of pharmacology. 102(1)
CGP 35348 (3-aminopropyl(diethoxymethyl)phosphinic acid) and 3-aminopropyl(n-hexyl)phosphinic acid (3-APHPA) were tested in the rat anococcygeus muscle against CGP 27492 (3-aminopropylphosphinic acid), a selective GABAB agonist, for their antagonist
Publikováno v:
British Journal of Pharmacology. 81:533-541
The effects of 5'-N-ethylcarboxamidoadenosine (NECA), L-NECA, 2-chloroadenosine, N6-phenylisopropyladenosine (L-PIA and D-PIA), cyclohexyladenosine (CHA), and adenosine were examined on the guinea-pig taenia coli. All the analogues except L-NECA caus
Publikováno v:
European Journal of Pharmacology. 99:287-293
Electrical field stimulation of the isolated pig bladder neck preparation initiated rapid non-adrenergic, non-cholinergic nerve-mediated relaxations. A wide range of substances were examined as possible candidates for the neurotransmitter involved. O
Publikováno v:
European journal of pharmacology. 88(4)
The effect of vasoactive intestinal polypeptide (VIP) on the electrical activity of the smooth muscle of the guinea-pig taenia coli has been examined using the single sucrose gap apparatus. VIP usually caused a slowly developing, long-lasting membran
Publikováno v:
Synapse (New York, N.Y.). 2(4)
Responses to substance P (SP) and to hypogastric nerve stimulation were recorded from voltage-clamped guinea pig inferior mesenteric ganglion (IMG) neurons, and compared with those to muscarine. Muscarine produced a voltage-dependent inward current a