“…Similar conclusions were obtained from the results of animal experiments and human observations, when we co-applied drugs acting on efferent and afferent vagal nerve fibres (Mózsik et al, 1997(Mózsik et al, , 2009) and received combined actions. Recently, different molecular-pharmacological observations were carried out (and calculated, based on the dose-responses curves of drugs) with capsaicin, atropine, pirenzepine, cimetidine, ranitidine, famotidine, nizatidine, omeprazole, esomeprazole, PGI 2, vitamin A, -carotene on the gastric basal acid output (BAO) in healthy human subjects (Mózsik et al, 2005), on changes of gastric transmucosal potential difference produced by ethanol (5 ml, 30 v/v% topically applied directly into the gastric mucosa by the way of endoscopic biopsy channel), on indomethacin-induced (3x25+25 mg orally) gastric microbleeding in healthy human subjects (Mózsik et al, 2007), and on gastric (basal and stimulated by betanechol, histamine and pentagastrin) acid secretion of pylorus-ligated rats or on gastric mucosal damage produced by different chemicals (Indomethacin, HCl, ethanol, NaOH, concentrated NaCl solution) in rats . The values of affinity (pD) and intrinsic activity ( ) curves of these compounds were calculated according to standard procedures employed in molecular-pharmacology (Csáky, 1969).…”