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.
CHICAGO
, "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,
VANCOUVER
. Opposite effect of naloxone on infertility induced by nitric oxide system in an animal model of polycystic ovary. Daneshvar Med. 2014;22(1):85-94 (In Persian).