Constanti, A. published the artcileAntagonism by some antihistamines of the amino acid-evoked responses recorded from the lobster muscle fiber and the frog spinal cord, Quality Control of 2508-72-7, the publication is British Journal of Pharmacology (1976), 58(4), 583-92, database is CAplus and MEDLINE.
On lobster muscle in vitro, histamine [51-45-6] H1 receptor blockers, e.g. antazoline-HCl (I-HCl) [2508-72-7] (40μM-1mM) reversibly antagonized responses to both-applied glutamate [56-86-0] (0.1mM), aspartate [56-84-8] (1 or 2 mM), or quisqualic acid [52809-07-1] (1-6μM), but not GABA [56-12-2] (40μM). Histamine (â?mM) had no effect on this preparation The H1 antagonists produced a small increase in muscle hyperpolarization; procaine [59-46-1] (1mM) decreased membrane conductance but did not affect responses to GABA or glutamate. The H2 antagonist burimamide (II) [34970-69-9] blocked glutamate and GABA-evoked responses on the lobster muscle without affecting resting potential or conductance. In the frog spinal cord, bath-applied histamine produced ventral root depolarizations and dorsal root hyperpolarizations which were reduced by tetrodotoxin but not by I or II; II reversibly antagonized responses to both glutamate and GABA on tetrodotoxin-treated cords whereas I was ineffective. Antihistamines may act as nonspecific amino acid antagonists by interacting at the level of the receptor-coupled ionophores.
British Journal of Pharmacology published new progress about 2508-72-7. 2508-72-7 belongs to imidazoles-derivatives, auxiliary class Inhibitor,Immunology/Inflammation,Histamine Receptor, name is N-Benzyl-N-((4,5-dihydro-1H-imidazol-2-yl)methyl)aniline hydrochloride, and the molecular formula is C17H20ClN3, Quality Control of 2508-72-7.
Referemce:
https://en.wikipedia.org/wiki/Imidazole,
Imidazole | C3H4N2 – PubChem