Moringa oleifera ethanolic extract ameliorates the testicular dysfunction resulted from HFD-induced obesity rat model.
Mohamed E AlkafafySamy M SayedAhmed M El-ShehawiSamir Ahmed El-ShazlySamy F MahmoudSaqer S AlotaibiDoaa A MadkourSahar Hassan OrabiHamed T ElbazMohamed Mohamed AhmedPublished in: Andrologia (2021)
In this study, we estimated the protective role of Moringa oleifera leaf ethanolic extract (MOLE) against obesity-associated testicular dysfunction. Fifty male albino rats were randomly assigned to five groups (n = 10): Group I (basal diet), group II (basal diet plus MOLE orally), group III (high-fat diet-HFD), group IV (HFD plus oral MOLE) and group V (HFD for 8 weeks followed by a basal diet plus oral MOLE for 6 weeks). The study duration extended for 14 weeks. Serum collected to investigate testosterone, FSH and LH levels. Testicular tissues were used to determine levels of SOD, glutathione, catalase and malondialdehyde. Semen was collected to estimate its quality (morphology, motility and concentration). Morphological changes in the testis were investigated by histopathological and immunohistochemical techniques. Compared with both control treatment and MOLE treatment, serum testosterone, FSH, LH, testicular enzymatic catalase, SOD, GSH, survivin immunoreactivity, sperm quality and testicular weight were all significantly decreased in rats treated with HFD, while there were significant increases in testicular malondialdehyde and caspase-3 immunoreactivity. MOLE improved all harmful effects of HFD. Improvements were more pronounced in the protected (G 4) than the treated (G 5) group. MOLE could be a potential solution for obesity-associated fertility problem.
Keyphrases
- high fat diet
- insulin resistance
- weight loss
- germ cell
- adipose tissue
- metabolic syndrome
- physical activity
- high fat diet induced
- oxidative stress
- type diabetes
- weight gain
- skeletal muscle
- replacement therapy
- gestational age
- escherichia coli
- quality improvement
- induced apoptosis
- high resolution
- cystic fibrosis
- risk assessment
- diabetic rats
- hydrogen peroxide
- mass spectrometry
- mouse model
- drug induced