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1.
Biomed Pharmacother ; 174: 116504, 2024 May.
Article in English | MEDLINE | ID: mdl-38552442

ABSTRACT

Polycystic ovary syndrome (PCOS) is the most common cause of anovulatory infertility. The aim of this study was to investigate the therapeutic potential of vitamin C, glutamine, mesalazine, hydralazine, and alendronate as new drug candidates for the treatment of letrozole-induced PCOS in female Wistar rats. PCOS was induced in rats by intramuscular injection of estradiol valerate (2 mg/kg body weight for 28 days). The rats then received normal saline (PCOS group), letrozole (0.5 mg/kg), vitamin C (100 mg/kg), glutamine (1000 mg/kg), mesalazine (200 mg/kg), hydralazine (30 mg/kg), and alendronate (17.5 mg/kg). Serum testosterone, LH, FSH, estradiol and progesterone levels were determined by ELISA method. H&E staining was used for histological analysis in the ovarian tissues. The groups treated with hydralazine and alendronate, show a significant decrease in testosterone, LH hormone, cystic and atretic follicles, and a significant increase in the number of single layer, multilayer, antral, graafian follicles and the volume of corpus luteum as compared to the PCOS group. Hydrolazine and alendronate appear to be effective in restoring folliculogenesis and increasing ovulation in PCOS rat. So that the natural process of ovulation and the improvement of the histology of polycystic ovaries and its shift towards healthy and active ovaries were observed. This finding supports the potential beneficial effect of hydrolazine and alendronate on improving PCOS complication.


Subject(s)
Alendronate , Aromatase Inhibitors , Hydralazine , Polycystic Ovary Syndrome , Animals , Female , Rats , Alendronate/pharmacology , Aromatase Inhibitors/pharmacology , Disease Models, Animal , Estradiol/blood , Hydralazine/pharmacology , Hydralazine/therapeutic use , Letrozole , Luteinizing Hormone/blood , Ovary/drug effects , Ovary/pathology , Polycystic Ovary Syndrome/drug therapy , Polycystic Ovary Syndrome/chemically induced , Polycystic Ovary Syndrome/pathology , Rats, Wistar , Testosterone/blood
2.
J Biomol Struct Dyn ; 41(24): 15507-15519, 2023.
Article in English | MEDLINE | ID: mdl-36940361

ABSTRACT

Polycystic ovary syndrome (PCOS) is the most common cause of infertility without ovulation. Aromatase inhibitors were first proposed as new ovulation-inducing drugs in anovulatory women with an inadequate response to clomiphene. Letrozole is an aromatase inhibitor used as an ovulation inducer in infertile women due to PCOS. However, there is no definitive treatment for women with PCOS and the treatments are mostly symptomatic. In this study, we intend to introduce alternative drugs to letrozole using the library of FDA-approved drugs and evaluate the interaction of these drugs with the aromatase receptor. For this aim, molecular docking was performed to identify interactions of FDA-approved drugs with essential residues in the active site of the aromatase receptor. 1614 FDA-approved drugs were docked with aromatase receptor using AutoDock Vina. Molecular dynamics (MD) simulation study was also performed for 100 ns to verify the stability of the drug-receptor complexes. MMPBSA analysis evaluate the binding energy of selected complexes. Finally, acetaminophen, alendronate, ascorbic acid, aspirin, glutamine, hydralazine, mesalazine and pseudoephedrine drugs showed the best results in interaction with aromatase receptor based on computational studies. These drugs can be introduced as an alternative to letrozole for treating PCOS.Communicated by Ramaswamy H. Sarma.


Subject(s)
Infertility, Female , Polycystic Ovary Syndrome , Female , Humans , Aromatase Inhibitors/pharmacology , Letrozole/therapeutic use , Polycystic Ovary Syndrome/drug therapy , Polycystic Ovary Syndrome/complications , Infertility, Female/drug therapy , Infertility, Female/etiology , Aromatase , Molecular Docking Simulation , Nitriles , Triazoles , Fertility Agents, Female/therapeutic use , Ovulation Induction/adverse effects , Ovulation Induction/methods
3.
Andrologia ; 52(6): e13604, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32324915

ABSTRACT

Cryopreservation is the most effective method for preserving semen for a long period of time. However, during the freeze-thaw process, production of reactive oxygen species (ROS) leads to a steep reduction in sperm fertility indices. In this study, we tested the effects of the extract of the coelomic cavity of five Holotheria parva, a marine organism rich in antioxidants, for its ROS-scavenging activity and cryoprotective effects on oxidative stress. Using a total of 50 semen samples, our results demonstrated that doses of 250 and 500 µg/ml of H. parva coelomic cavity extract significantly increased sperm vitality as compared to the control (p < .05). The addition of 250 µg/ml of the extract exerted a significant positive effect on sperm motility. Moreover, sperm DNA damage and ROS production were significantly reduced at extract concentrations of 250 and 500 µg/ml (p < .05). To the best of our knowledge, the results of this study represent the first demonstration of the possibility of improving sperm parameters and reducing ROS production and DNA damage by supplementing sperm freezing media with H. parva coelomic extract. Our results suggested that H. parva coelomic extract could be useful for improving the fertilising ability of frozen-thawed human semen.


Subject(s)
Cryopreservation , DNA Damage/drug effects , Free Radical Scavengers/pharmacology , Holothuria , Oxidative Stress/drug effects , Semen Preservation , Spermatozoa/drug effects , Tissue Extracts/pharmacology , Animals , Cell Survival , Chromatin/drug effects , Humans , Male , Pilot Projects , Reactive Oxygen Species/metabolism , Semen Analysis , Sperm Motility/drug effects
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