[Histamine receptors in the human saphenous vein]. 1978

L Zappia, and G Melotti, and P Bocchi, and G Bertaccini

UI MeSH Term Description Entries
D010632 Pheniramine One of the HISTAMINE H1 ANTAGONISTS with little sedative action. It is used in treatment of hay fever, rhinitis, allergic dermatoses, and pruritus. Histapyridamine,Propheniramine,Prophenpyridamine,Avil,Daneral,Pheniramine Bimaleate,Pheniramine Maleate,Bimaleate, Pheniramine,Maleate, Pheniramine
D011968 Receptors, Histamine Cell-surface proteins that bind histamine and trigger intracellular changes influencing the behavior of cells. Histamine receptors are widespread in the central nervous system and in peripheral tissues. Three types have been recognized and designated H1, H2, and H3. They differ in pharmacology, distribution, and mode of action. Histamine Binding Sites,Histamine Receptors,Histamine Receptor,Binding Sites, Histamine,Receptor, Histamine,Sites, Histamine Binding
D011969 Receptors, Histamine H1 A class of histamine receptors discriminated by their pharmacology and mode of action. Most histamine H1 receptors operate through the inositol phosphate/diacylglycerol second messenger system. Among the many responses mediated by these receptors are smooth muscle contraction, increased vascular permeability, hormone release, and cerebral glyconeogenesis. (From Biochem Soc Trans 1992 Feb;20(1):122-5) H1 Receptor,Histamine H1 Receptors,H1 Receptors,Histamine H1 Receptor,Receptors, H1,H1 Receptor, Histamine,H1 Receptors, Histamine,Receptor, H1,Receptor, Histamine H1
D002927 Cimetidine A histamine congener, it competitively inhibits HISTAMINE binding to HISTAMINE H2 RECEPTORS. Cimetidine has a range of pharmacological actions. It inhibits GASTRIC ACID secretion, as well as PEPSIN and GASTRIN output. Altramet,Biomet,Biomet400,Cimetidine HCl,Cimetidine Hydrochloride,Eureceptor,Histodil,N-Cyano-N'-methyl-N''-(2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)guanidine,SK&F-92334,SKF-92334,Tagamet,HCl, Cimetidine,Hydrochloride, Cimetidine,SK&F 92334,SK&F92334,SKF 92334,SKF92334
D006632 Histamine An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter. Ceplene,Histamine Dihydrochloride,Histamine Hydrochloride,Peremin
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012501 Saphenous Vein The vein which drains the foot and leg. Saphenous Veins,Vein, Saphenous,Veins, Saphenous
D013890 Thiourea A photographic fixative used also in the manufacture of resins. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), this substance may reasonably be anticipated to be a carcinogen (Merck Index, 9th ed). Many of its derivatives are ANTITHYROID AGENTS and/or FREE RADICAL SCAVENGERS.

Related Publications

L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
January 1989, Pharmacology & toxicology,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
January 1999, European journal of pharmacology,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
July 1992, Naunyn-Schmiedeberg's archives of pharmacology,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
September 1986, British journal of pharmacology,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
May 1994, European journal of pharmacology,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
January 2003, Bulletin of experimental biology and medicine,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
April 1999, Journal of cardiovascular pharmacology,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
December 1995, Japanese journal of pharmacology,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
August 1993, European journal of pharmacology,
L Zappia, and G Melotti, and P Bocchi, and G Bertaccini
July 2011, Current vascular pharmacology,
Copied contents to your clipboard!