1994
DOI: 10.1136/bmj.308.6927.503
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Risk of gynaecomastia associated with cimetidine, omeprazole, and other antiulcer drugs

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Cited by 79 publications
(29 citation statements)
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“…Gynecomastia has also been associated with digitalis and spironolactone (14), which interfere with the production of testosterone and its conversion to the potent metabolite, 5-alfa-dihydrotestosterone (4,10). Cimetidine is also a precursor of gynecomastia (15). Fibroadenomas in men without hormone treatment and with normal hormone levels are extremely rare.…”
Section: Discussionmentioning
confidence: 99%
“…Gynecomastia has also been associated with digitalis and spironolactone (14), which interfere with the production of testosterone and its conversion to the potent metabolite, 5-alfa-dihydrotestosterone (4,10). Cimetidine is also a precursor of gynecomastia (15). Fibroadenomas in men without hormone treatment and with normal hormone levels are extremely rare.…”
Section: Discussionmentioning
confidence: 99%
“…Hence, we investigated the mRNA levels of representative genes which, especially in the first few hours after hepatectomy (“priming phase”), are of particular importance [2,21]. Additionally, a connection to the previously proven effects of argon on these genes should exist [8,13].…”
Section: Resultsmentioning
confidence: 99%
“…Experimental studies have been able to identify a set of substances and signals which are indispensable for liver regeneration (LR) [2,3]. These include various transcription factors, cytokines, growth factors, and intracellular signaling events which, in a complex, well-orchestrated interaction, are capable of initiating, advancing, and ending this process.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…The stage is catalyzed by cyclooxygenase (COX) within which isoenzymes COX-1 and COX-2 occur [11]. The variations in the adverse effects of NSAIDs at their anti-inflammatory doses are due to the individual NSAIDs exhibiting dissimilar potencies against COX-1 in comparison to COX-2 [12]. Most of NSAIDs exhibit more selectivity for COX-1 than for COX-2, and this forms the basis for their gastro-toxicity and their anti-thrombotic action [13].…”
Section: Introductionmentioning
confidence: 99%