TY - JOUR
T1 - The effect of nizatidine on duodenal ulcer healing and on mucosal inflammatory mediators
AU - Eliakim, R.
AU - Stalnikowicz, R.
AU - Ackerman, Z.
AU - Karmeli, F.
AU - Rachmilewitz, D.
PY - 1994/10
Y1 - 1994/10
N2 - The aim of this double-blind, randomized, placebo-controlled trial was to evaluate the effect of nizatidine on duodenal ulcer healing and generation of mucosal prostaglandin estradiol and inflammatory mediators. Fifty-five patients with endoscopically proven active duodenal ulcer received either nizatidine 300 mg or placebo, once nightly, for 4 weeks, when a second endoscopy was performed. Healing was defined as complete epithelialization of the ulcer crater. At both endoscopies mucosal biopsies were obtained for determination of prostanoids and inflammatory mediators. Nizatidine and placebo induced ulcer healing in 76% and 60.9% of the patients, respectively, but the difference did not reach statistical significance. Nizatidine treatment did not significantly affect mucosal leukotriene B4, leukotriene C4 or platelet activating factor generation. It is concluded, therefore, that the antisecretory effect is probably the main mechanism responsible for nizatidine's therapeutic effects in peptic ulcer disease.
AB - The aim of this double-blind, randomized, placebo-controlled trial was to evaluate the effect of nizatidine on duodenal ulcer healing and generation of mucosal prostaglandin estradiol and inflammatory mediators. Fifty-five patients with endoscopically proven active duodenal ulcer received either nizatidine 300 mg or placebo, once nightly, for 4 weeks, when a second endoscopy was performed. Healing was defined as complete epithelialization of the ulcer crater. At both endoscopies mucosal biopsies were obtained for determination of prostanoids and inflammatory mediators. Nizatidine and placebo induced ulcer healing in 76% and 60.9% of the patients, respectively, but the difference did not reach statistical significance. Nizatidine treatment did not significantly affect mucosal leukotriene B4, leukotriene C4 or platelet activating factor generation. It is concluded, therefore, that the antisecretory effect is probably the main mechanism responsible for nizatidine's therapeutic effects in peptic ulcer disease.
KW - Duodenal ulcer
KW - Estradiol
KW - Gastrin
KW - Leukotriene B
KW - Leukotriene C
KW - Platelet activating factor
KW - Prostaglandin
UR - http://www.scopus.com/inward/record.url?scp=0028518788&partnerID=8YFLogxK
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AN - SCOPUS:0028518788
SN - 0021-2180
VL - 30
SP - 751
EP - 756
JO - Israel Journal of Medical Sciences
JF - Israel Journal of Medical Sciences
IS - 10
ER -