Author/Authors :
Rezazadeh, Hossein rafsanjan university of medical sciences - Physiology-Pharmacology Research Center, ايران , Hosseini Kahnouei, Mohammadamin rafsanjan university of medical sciences - Physiology-Pharmacology Research Center, ايران , Hassanshahi, Gholamhossein rafsanjan university of medical sciences - Molecular Medicine Research Center, ايران , Allahtavakoli, Mohammad rafsanjan university of medical sciences - Physiology-Pharmacology Research Center, ايران , Shamsizadeh, Ali rafsanjan university of medical sciences - Physiology-Pharmacology Research Center, ايران , Roohbakhsh, Ali rafsanjan university of medical sciences - Physiology-Pharmacology Research Center, ايران , Fatemi, Iman rafsanjan university of medical sciences - Physiology-Pharmacology Research Center, ايران , Zarisfi, Mohammadreza rafsanjan university of medical sciences - Physiology-Pharmacology Research Center, ايران , Pourshanazari, Ali Asghar rafsanjan university of medical sciences - Physiology-Pharmacology Research Center, ايران , Pourshanazari, Ali Asghar isfahan university of medical sciences - School of Medicine - Department of Physiology, ايران
Abstract :
Introduction. Opiates are traditionally used for treatment of some acute heart disorders. There are only few reports on the effects of long-term treatment of cardiovascular diseases with morphine. This study aimed to investigate the effects of chronic low-dose morphine use on the cardiovascular system in two-kidney one-clip (2K1C) hypertensive rats. Materials and Methods. Male Wistar rats were divided into two groups as the sham and 2K1C groups and each group was further subdivided into saline and morphine treatment subgroups. Blood pressure, heart rate, plasma rennin activity, serum nitric oxide concentration, and baroreflex sensitivity were measured. Results. Morphine significantly attenuated systolic blood pressure, diastolic blood pressure, and mean arterial pressure in the 2K1C animals. In addition, morphine decreased plasma rennin activity in the 2K1C group. Serum concentrations of nitric oxide were also decreased, and morphine prevented the reduction of nitric oxide. The baroreflex sensitivity was also improved following morphine administration in the 2K1C group. Conclusions. According to the results presented in this study, chronic administration of low-dose morphine reduces regulated hypertension in the 2K1C rats, probably via a nitric oxide-dependent pathway.
Keywords :
baroreflex sensitivity , morphine , nitric oxide , rennin activity , rats