Resveratrol benefits on sperm DNA, chromatin structure and reproductive outcomes of varicocelized rats.
Talita Biude MendesJoana Noguères SimasLeonardo Wensing FischerCamila Cicconi PaccolaSamara Urban de OlivaVanessa VendraminiSandra Maria MiragliaPublished in: Andrologia (2022)
In varicocele, the main cause of sperm DNA damage is oxidative stress (OS). Resveratrol, a polyphenol with antioxidant properties, can protect cells from injuries caused by OS. We investigated the benefits of resveratrol against reproductive damage caused by experimental varicocele induced from peripuberty. Eighty peripubertal male rats were distributed into 4 groups: sham-control (S), varicocele (V), resveratrol (R) and varicocele treated with resveratrol (VR). Varicocele was induced through the partial ligature of the left renal vein. Resveratrol was given in a daily dose of 300 mg/kg body weight (gavage). Sperm samples were collected at 100 days of age for vitality, DNA fragmentation and chromatin protamination evaluations. OS analyses were carried out. Rats from all groups were mated with healthy primiparous females for evaluation of reproductive capacity and embryonic quality. The V group showed reduction of sperm vitality, altered chromatin protamination and sperm DNA integrity and high levels of OS. The VR group showed an improvement of oxidative status, sperm vitality, DNA integrity and chromatin structure, and an enhancement in the gestational index and embryonic quality. Therefore, we showed in this experimental model that resveratrol is a promising nutraceutical adjuvant and should be deeply studied to mitigate subfertility in varicocele.
Keyphrases
- dna damage
- oxidative stress
- circulating tumor
- diabetic rats
- cell free
- gene expression
- body weight
- transcription factor
- genome wide
- single molecule
- dna repair
- pregnant women
- high glucose
- physical activity
- clinical trial
- drug induced
- weight gain
- mass spectrometry
- nucleic acid
- quality improvement
- body mass index
- insulin resistance
- circulating tumor cells
- solid state