Publication: Nitric oxide contributes to desipramine- induced hypotension in rats
Issued Date
1996-01-01
Resource Type
ISSN
09603271
Other identifier(s)
2-s2.0-0029918002
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Mahidol University
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SCOPUS
Bibliographic Citation
Human & Experimental Toxicology. Vol.15, No.4 (1996), 320-328
Suggested Citation
P. R. Pentel, W. Wananukul, W. Scarlett, D. E. Keylerl, P. R. Pentel, D. E. Keylerl Nitric oxide contributes to desipramine- induced hypotension in rats. Human & Experimental Toxicology. Vol.15, No.4 (1996), 320-328. doi:10.1177/096032719601500408 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/17605
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Title
Nitric oxide contributes to desipramine- induced hypotension in rats
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. © 1996, Sage Publications. All rights reserved.