Cinnamtannin B-1, a novel antioxidant for sperm in red deer
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
29776697
DOI
10.1016/j.anireprosci.2018.05.004
PII: S0378-4320(18)30112-X
Knihovny.cz E-resources
- Keywords
- Antioxidant, Cinnamtannin B-1, Deer-, Sperm oxidative stress,
- MeSH
- Antioxidants pharmacology MeSH
- DNA Fragmentation MeSH
- Sperm Motility drug effects MeSH
- Oxidative Stress drug effects MeSH
- Lipid Peroxidation MeSH
- Proanthocyanidins pharmacology MeSH
- Reactive Oxygen Species metabolism MeSH
- Spermatozoa drug effects MeSH
- Semen Preservation veterinary MeSH
- Cell Survival drug effects MeSH
- Deer * MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antioxidants MeSH
- cinnamtannin B-1 MeSH Browser
- Proanthocyanidins MeSH
- Reactive Oxygen Species MeSH
Cinnamtannin B-1 (CNB-1) is a naturally occurring trimeric A-type proanthocyanidin contained in several plants such as cinnamon (Cinnamomum zeylanicum). It is considered to be a potent antioxidant. The protective effect of CNB-1 against oxidative stress was assessed in red deer epididymal sperm incubated at 37 °C. Cryopreserved sperm from six stags were thawed, pooled and extended to 400 × 106 sperm/ml in BGM (bovine gamete medium). After being aliquoted, the samples were supplemented with different concentrations of CNB-1 (0, 0.1, 1, 10 and 100 μg/mL), with or without induced oxidative stress (100 μM Fe2+/ascorbate). The samples were evaluated after 0, 2 and 4 h of incubation at 37 °C. This experiment was replicated six times. Spermmotility (CASA), viability, mitochondrial membrane potential, acrosomal status, lipoperoxidation (C11 BODIPY 581/591), intracellular reactive oxygen species (ROS) production and DNA status (TUNEL) were assessed. After 4 h of incubation, CNB-1 prevented the deleterious effects of oxidative stress, thus improved sperm progressivity and velocity (P<0.05). Furthermore, 1 and 10 μM CNB-1 improved sperm linearity, even when compared to those samples that had not been subjected to oxidative stress (P<0.05). The greatest concentration, 100 μM, prevented sperm lipoperoxidation and reduced ROS production in samples subjected to oxidative stress.
Biomedical Center Medical Faculty in Pilsen Pilsen Czech Republic
Department of Molecular Biology University of León León Spain
Faculty of Pharmacy Albacete Spain
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