1979
DOI: 10.1016/0006-2952(79)90441-6
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Inhibition of hepatic gluconeogenesis by phenethylhydrazine (phenelzine)

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1983
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Cited by 13 publications
(2 citation statements)
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“…As indicated above, the non-selective MAO inhibitor phenelzine is also an SSAO inhibitor [10]. In addition, owing to its hydrazine structure and not to MAOI considerations, phenelzine has been reported to induce hypoglycaemia in animal models and in depressed patients through the impairment of gluconeogenesis, likely as a consequence of phosphoenolpyruvatecarboxykinase (PEPCK) inhibition [47]. Since phenelzine is an old drug prescribed for antidepressant therapy, with no clear evidence of the serious adverse effects attributed to hydrazines as discussed above, it is a good candidate for drug repositioning.…”
Section: Combining the Inhibition Effect Of Maos And Aocs On Adipomentioning
confidence: 99%
“…As indicated above, the non-selective MAO inhibitor phenelzine is also an SSAO inhibitor [10]. In addition, owing to its hydrazine structure and not to MAOI considerations, phenelzine has been reported to induce hypoglycaemia in animal models and in depressed patients through the impairment of gluconeogenesis, likely as a consequence of phosphoenolpyruvatecarboxykinase (PEPCK) inhibition [47]. Since phenelzine is an old drug prescribed for antidepressant therapy, with no clear evidence of the serious adverse effects attributed to hydrazines as discussed above, it is a good candidate for drug repositioning.…”
Section: Combining the Inhibition Effect Of Maos And Aocs On Adipomentioning
confidence: 99%
“…In addition, an overdose can lead to fainting, excessive sweating, a rapid pulse, and shallow breathing. 6,7 Moreover, PZ has a toxic reaction in the liver, leading to liver damage. Alternatively, propofol (PPF) is a short-acting intravenous anaesthetic used for the induction and maintenance of general anaesthesia.…”
Section: Introductionmentioning
confidence: 99%