Resistance of cholestatic rats against epinephrine-induced arrhythmia: The role of nitric oxide and endogenous opioids

Amir Reza Hajrasouliha, Sina Tavakoli, Pejman Jabehdar-Maralani, Hamed Shafaroodi, Amir Ali Borhani, Golbahar Houshmand, Hamed Sadeghipour, Mehdi Dehghani, Ahmad Reza Dehpour

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16 Scopus citations

Abstract

Short-term ligation of bile duct has been used as a model to study acute cholestasis and is associated with various cardiovascular abnormalities. We examined the role of nitric oxide (NO) and endogenous opioids on epinephrine-induced arrhythmia in 7-day bile duct-ligated (BDL) rats. Six groups of rats, each of which was subdivided into two subgroups (sham-operated and BDL), were examined. First group of animals were chronically treated with normal saline. In the second and third groups, single intraperitoneal administration of N(ω)-nitro-l-arginine methyl ester (l-NAME, 10 mg/kg) or naltrexone (20 mg/kg) was performed 30 min before evaluation of epinephrine-induced arrhythmia. Two groups received chronic administration of low dose (3 mg/kg/day) or high dose (10 mg/kg/day) l-NAME; and the last group was treated chronically with naltrexone (20 mg/kg/day). Chronic drug administration was performed subcutaneously for 6 consecutive days following BDL or sham operation. After induction of arrhythmia by intravenous injection of 10 μg/kg epinephrine, mean arterial pressure and electrocardiogram were recorded for 1 min. Heart rate and mean arterial pressure were significantly lower in BDL rats (P<0.01). Chronic injection of naltrexone increased heart rate and mean arterial pressure in BDL (P<0.05). Chronic low dose l-NAME administration had no effect on baseline hemodynamic parameters. High dose l-NAME injection corrected hypotension in BDL rats, but not bradycardia (P<0.05). Epinephrine induced less arrhythmia in BDL rats (P<0.05). Acute and chronic injection of naltrexone had no effect on the resistance of BDL rats against epinephrine-induced arrhythmia. Although acute l-NAME administration enhanced arrhythmias in sham-operated rats (P<0.001), it had no effect on BDL animals. Chronic injection of low dose or high dose l-NAME, without having any effect on sham-operated animals, increased arrhythmias in BDL rats (P<0.01). This study showed that BDL animals are resistant against epinephrine-induced arrhythmia and this resistance depends on long-term NO overproduction.

Original languageEnglish (US)
Pages (from-to)307-313
Number of pages7
JournalEuropean Journal of Pharmacology
Volume499
Issue number3
DOIs
StatePublished - Sep 24 2004

Keywords

  • (Rat)
  • Cholestasis
  • Endogenous opioids
  • Epinephrine-induced arrhythmia
  • NO (Nitric oxide)

ASJC Scopus subject areas

  • Pharmacology

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  • Cite this

    Hajrasouliha, A. R., Tavakoli, S., Jabehdar-Maralani, P., Shafaroodi, H., Borhani, A. A., Houshmand, G., Sadeghipour, H., Dehghani, M., & Dehpour, A. R. (2004). Resistance of cholestatic rats against epinephrine-induced arrhythmia: The role of nitric oxide and endogenous opioids. European Journal of Pharmacology, 499(3), 307-313. https://doi.org/10.1016/j.ejphar.2004.07.099