Background and Objective: Evidence exist that polycystic ovarian syndrome (PCOS) is responsible for a high percentage of women infertility during reproductive age. In this study, the correction of this problem by hyper-activation of nitric oxide (NO) system was studied in rats.
Materials and Methods: Female Wistar rats (weighing 200-250 g) were kept as virgin diestrous under standard conditions. One group of the rats was i.p. injected with L-arginine (50 mg/kg) through a period lasting nine days/once a day. Another group received naloxone (0.4 mg/kg), 30 min prior to i.p. injection of L-arginine during the experimental phase. The third group was injected with a single dose of naloxone (0.4 mg/kg, i.p.). The control group solely received saline (1 ml/kg, i.p.).
Results: Ovaries from L-arginine treated rats showed polycystic characteristics in comparison with the control this feature was resolved in the naloxone treated groups. The endometrium due to L-arginine showed inflammation, however, its growth or folding were significant in naloxone treated rats.
Conclusion: Naloxone intervenes with the PCOS induced by over-activation of NOS. This research likely represents the case of infertility in the animal model of PCOS. The study may open a new gate towards the naloxone efficacy on infertility induced of PCOS.
(2014). Opposite effect of naloxone on infertility induced by nitric oxide system in an animal model of polycystic ovary. Daneshvar Medicine, 22(1), 85-94.
MLA
. "Opposite effect of naloxone on infertility induced by nitric oxide system in an animal model of polycystic ovary". Daneshvar Medicine, 22, 1, 2014, 85-94.
HARVARD
(2014). 'Opposite effect of naloxone on infertility induced by nitric oxide system in an animal model of polycystic ovary', Daneshvar Medicine, 22(1), pp. 85-94.
VANCOUVER
Opposite effect of naloxone on infertility induced by nitric oxide system in an animal model of polycystic ovary. Daneshvar Medicine, 2014; 22(1): 85-94.