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1.
Pol J Vet Sci ; 25(1): 5-12, 2022 Mar.
Article in English | MEDLINE | ID: mdl-35575768

ABSTRACT

In this study, the cryoprotective effect of different doses of propolis (P) on bull semen, which has solid pharmacological properties thanks to its rich phenolic components, was investigated biochemically and physiologically. Semen samples were collected from Simmental breed bulls via the artificial vagina and pooled. After dividing into five groups, control (C: no additive) and four different P (200, 100, 50, and 25 µg/mL) groups, the final concentration was diluted to 16×106 per straw. Semen samples were equilibrated at 4°C for approximately 4 hours, then placed in French straws and frozen. After thawing, sperm motility and kinetic parameters, DNA integrity by single-cell gel electrophoresis, sperm abnormalities by liquid fixation, and lipid peroxidation levels by the colorimetric method was analyzed by Computer-Assisted Semen Analyzer. P added to the diluent showed no effect on motility and kinetic parameters at P25 and P50 (p>0.05), while P100 and P200 had a negative effect (p⟨0.001). The addition of P (25 and 50) showed a treatment effect on tail abnormality compared to C (p⟨0.05). Especially P50 had a positive effect on tail length, tail DNA, and tail movement, while P100 and P200 caused DNA damage (p⟨0.001). MDA levels increased in all P dose groups compared to C (p⟨0.001). This study has clearly demonstrated that P25 and P50 supplements could be used therapeutically to treat sperm tail abnormalities and prevent DNA damage in post-thawed bull sperm.


Subject(s)
Propolis , Semen Preservation , Animals , Cattle , Cryopreservation/veterinary , Cryoprotective Agents/pharmacology , DNA , Female , Male , Propolis/pharmacology , Semen , Semen Analysis/veterinary , Semen Preservation/methods , Semen Preservation/veterinary , Sperm Motility , Spermatozoa/physiology
2.
Andrologia ; 50(7): e13036, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29761542

ABSTRACT

In this study, the reproductive impacts of being exposed to glyphosate (GLF) and the protective impacts of resveratrol (RES) were assessed in 28 Wistar male rats, which were equally separated into four groups. Control group were fed normal diet without GLF or RES, group II received normal feed containing 20 mg kg-1 daily-1 RES, group III received normal feed containing 375 mg kg-1 daily-1 GLF, and group IV received normal feed containing 375 mg kg-1 daily-1 GLF+20 mg kg-1 daily-1 RES. GLF administration decreased sperm motility, sperm plasma membrane integrity, glutathione level and superoxide dismutase in the testicular tissue of rats. On the other hand, abnormal sperm rate, malondialdehyde level, and DNA damage were detected to be high in the group treated with GLF. The findings indicate that RES protects spermatological parameters and DNA damage, decreases GLF-induced lipid peroxidation, improves the antioxidant defence mechanism and regenerates tissue damage in the testis of rats.


Subject(s)
Antioxidants/pharmacology , Herbicides/toxicity , Infertility, Male/prevention & control , Resveratrol/pharmacology , Testis/drug effects , Animals , Antioxidants/therapeutic use , DNA Damage/drug effects , Disease Models, Animal , Environmental Pollutants/toxicity , Glycine/analogs & derivatives , Glycine/toxicity , Humans , Infertility, Male/chemically induced , Infertility, Male/pathology , Male , Oxidative Stress/drug effects , Rats , Rats, Wistar , Resveratrol/therapeutic use , Sperm Count , Sperm Motility/drug effects , Testis/pathology , Treatment Outcome , Glyphosate
3.
Cryo Letters ; 39(2): 156-165, 2018.
Article in English | MEDLINE | ID: mdl-29734425

ABSTRACT

BACKGROUND: Cryopreservation has a side effect on the motility, chromatin integrity and viability of sperm cells. OBJECTIVE: The present study investigated the effects of supplementation with rosmarinic acid (RA) Tris extender on sperm quality parameters, plasma and acrosome membrane damage, antioxidant enzyme activity and chromatin integrity following the freeze thawing process on bull spermatozoa. MATERIALS AND METHODS: Ejaculates were split into five aliquots and diluted to a final concentration of 15x106 spermatozoa per ml with the Tris extender containing RA (25, 50, 100 and 200 microgram per ml) and (control) and then frozen at a controlled rate. RESULT: Treatments did not give better results on the percentages of sperm progressive, total motility and sperm motion characters (P >0.05); however, RA25 and RA50 exhibited favourable chromatin integrity. In conclusion, RA25 and RA50 increased total antioxidant activity. As a consequence, the amount of MDA and chromatin damage were reduced in sperm cells.


Subject(s)
Cinnamates/pharmacology , Cryopreservation/methods , Cryoprotective Agents/pharmacology , Depsides/pharmacology , Semen Preservation/methods , Spermatozoa/drug effects , Animals , Antioxidants/pharmacology , Cattle , Male , Oxidative Stress/drug effects , Sperm Motility/drug effects , Rosmarinic Acid
4.
Andrologia ; 2018 Feb 07.
Article in English | MEDLINE | ID: mdl-29411886

ABSTRACT

The aim of this study was to identify the effects of adding quercetin (Q) to Tris extender in order to identify levels of oxidative stress in bull sperm after freeze thawing. Ejaculates were collected via artificial vagina from Holstein bulls. Semen was divided into five tools and diluted to a final concentration of 15 × 106 spermatozoa/ml with the Tris extender containing Q (25, 50, 100 and 200 µg/ml) and no additive (control; C). All examples were equilibrated at 4°C during 4 hr then were loaded into 0.25-ml straws and frozen using a controlled rate. Sperm motility and motility characteristics were determined using the computer-assisted semen analyser. Sperm membrane integrity was assessed using the hypoosmotic swelling test. Sperm chromatin integrity was investigated using the single cell gel electrophoresis. Total antioxidant capacities were performed colorimetrically. Q supplementation used as an antioxidant did not produce better results in the proportion of sperm progressive and total motility, plasma membrane integrity and sperm abnormalities. Q supplementation exhibited the favourable tail length, tail DNA and tail moment. In conclusion, when whole parameters are considered, Q25 can be added to the Tris extender due to its positive effect on sperm DNA integrity and no adverse effect on the progressive and total motilities of sperm.

5.
Auton Autacoid Pharmacol ; 31(3-4): 50-6, 2011.
Article in English | MEDLINE | ID: mdl-21951584

ABSTRACT

1 The aim of this study was to clarify the effect of boric acid on contractions of rat isolated ileum. 2 Contractile responses expressed as Emax and pD2 for acetylcholine (10(-3)-10(-8) m, Ach), bethanechol (10(-3)-10(-8) m) and potassium (10-80 × 10(-3) m, KCl) were determined in the absence and presence of boric acid (10(-3); 5 × 10(-4); 10(-4) m). 3 The contractile response to Ach in the presence of verapamil (10(-6) or 10(-8) m) or in calcium-free Tyrode's solution was also determined in the absence and presence of boric acid. 4 Boric acid did not affect the contractile response to Ach, bethanechol or KCl. Single or cumulative treatment of boric acid did not affect ileum muscle contraction evoked by KCl. The atropine-resistant component of Ach-induced contraction and 4-diphenyl-acetoxy-N-methyl-piperidine methiodide-resistant component of bethanechol-induced contraction were not inhibited by boric acid (10(-3) m). The contractile response to Ach was reduced in calcium-free Tyrode's solution, and the contractile response was not affected by (10(-8) m). The addition of boric acid (10(-3) m) in combination with verapamil (10(-8) m) did not significantly affect the contractile response to Ach. 5 In conclusion, boric acid does not affect contractions induced by Ach, bethanechol or potassium in rat isolated ileum.


Subject(s)
Acetylcholine/pharmacology , Bethanechol/pharmacology , Boric Acids/pharmacology , Ileum/drug effects , Muscle Contraction/drug effects , Potassium Chloride/pharmacology , Animals , Atropine/pharmacology , Dose-Response Relationship, Drug , Drug Interactions , In Vitro Techniques , Male , Piperidines/pharmacology , Rats , Rats, Sprague-Dawley , Trace Elements/pharmacology , Verapamil/pharmacology
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