Nitric oxide contributes to desipramine- induced hypotension in rats

P. R. Pentel, W. Wananukul, W. Scarlett, D. E. Keylerl, D. E. Keylerl

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

1 Anesthetized rats received the TCA desipramine (DMI) 60 mg kg-1G-nitro-L-arginine methyl ester-(L-NAME) 15 min after DMI reversed hypotension within 5 min (P < 0.05). In contrast to its beneficial effect on blood pressure, L-NAME worsened DMI-induced prolongation of the electrocardiographic QRS interval. Dexamethasone, an inhibitor of NOS induction, did not prevent DMI-induced hypotension. 2 To study the effect of L-NAME on survival, DMI was administered to anesthetized rats as a continuous i.v. infusion until death. Despite initially improving blood pressure, L-NAME decreased the mean survival time by 33% (P < 0.01) compared to control treatment. Adminis tration of the nitric oxide (NO) donor nitroglycerine to rats during DMI infusion likewise decreased the mean survival time. 3 L-NAME partially reversed the hypotensive effect of nitroprusside in both anesthetized and awake rats. 4 These data suggest that NO production attributable to constitutive NOS (cNOS) activity aggravates the hypoten sion associated with DMI toxicity in the anesthetized rat, and contributes to the pathophysiology of this overdose. The shortened survival time produced by both increasing and decreasing NO production suggests that cNOS activity during DMI overdose is regulated and adaptive. Ongoing cNOS activity also contributed to nitroprusside-induced hypotension, and may represent a feature common to other drug-induced hypotensive states.

Original languageEnglish (US)
Pages (from-to)320-328
Number of pages9
JournalHuman & Experimental Toxicology
Volume15
Issue number4
DOIs
StatePublished - Apr 1996

Keywords

  • L-NAME (NG-nitro-L-arginine methyl ester- (L-NAME)
  • Tricyclic antidepressant
  • desipramine
  • nitric oxide
  • nitroprusside
  • toxicity

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