Acute Porphyria Drug Database

C01DA08 - Isosorbide Dinitrate
Not porphyrinogenic
NP

Rationale
No evidence of capacity for CYP-induction. CYP-mediated formation of nitric oxide from nitrate is of no clinical significance in humans. Three patient reports (N=3) supports the clinical evidence of non-porphyrogenicity.
Chemical description
1,4:3,6-Dianhydro-d-glucitol 2,5-dinitrate. Non-cyclic organic dinitrate. M= 236.1.
Therapeutic characteristics
Isosorbide dinitrate is a vasodilator with general properties similar to those of glyceryl trinitrate. It is used in the management of angina pectoris and of heart failure. It has also been investigated in myocardial infarction. Peroral administration, tablets (5, 10, 20, 40 mg) masticated (in acute angina) or swallowed. Individual dose and duration of therapy. Nausea and tachycardia are common side effects.
Hepatic exposure
Insignificant.
Metabolism and pharmakokinetics
Isosorbide dinitrate is widely distributed with a large apparent volume of distribution. It is taken up by smooth muscle cells of blood vessels and the nitrate group is cleaved to inorganic nitrite and then to nitric oxide. It is also rapidly metabolised in the liver to the major active metabolites isosorbide 2-mononitrate and isosorbide 5-mononitrate. No human data regarding avenues of biotransformation of organic nitrates by CYP-mediated oxidation, like in rats. It can be excluded that activation of PXR/CAR should be accomplished by an inorganic nitrogen compound, and that it should be accompanied by induction of ALAS1. No interferences with CYP-metabolism of other drugs observed.
Preclinical data
Rodent experiments suggest that the biotransformation of inrganic nitrates formed may take place by direct interaction with the heme moiety of cytochrome P450 and by isoenzymes induced by phenobarbital. McDonald Benett 1990. Cytochrome P450 mediated biotransformation of organic nitrates. PMID 2128204.
Personal communication
Andersson 2004: 1 patient report (tolerated).
Published experience
Kauppinen and Mustajoki 1992. Prognosis of acute porphyria: Occurrence of acute attacks, precipitating factors, and assocciated diseases. Medicine 1992; 71, 1-13. Two patient reports (tolerated n=2).
IPNet drug reports
Uneventful use reported in 3 patient with acute porphyria.

References

  1. Scientific articles
  2. Bogaert 1994. Clinical pharmacokinetics of nitrates. PMID 7873466. PMID 7873466. #4383
  3. Kauppinen and Mustajoki 1992. Prognosis of acute porphyria: Occurrence of acute attacks, precipitating factors, and assocciated diseases. Medicine 1992; 71, 1-13. #3278
  4. Mayer, Beretta 2008. The engima of nitroglycerin bioactivation and nitrate tolerance: views and troubles. PMID 18574453. PMID 18574453. #4793
  5. McDonald Benett 1990. Cytochrome P450 mediated biotransformation of organic nitrates. PMID 2128204. PMID 2128204. #4384
  6. Servent et al. Nitric oxide formation during microsomal hepatic denitration of glyceryl trinitrate. PMID 2506859. PMID 2506859. #4792
  7. Drug reference publications
  8. Martindale 2009 #3265

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