Stimulating effects of Quercetin (QUE) in tris citric acid extender on post thaw quality and in vivo fertility of buffalo (Bubalus bubalis) bull spermatozoa

Aim of this study was to evaluate the stimulating effects of quercetin (QUE) on post thaw quality and in vivo fertility of buffalo (Bubalus bubalis) bull spermatozoa. QUE is a well-known flavonoid having antioxidant properties to scavenge free radicals. Semen was collected from three buffalo bull th...

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Published inTheriogenology Vol. 134; pp. 18 - 23
Main Authors Ahmed, Hussain, Jahan, Sarwat, Salman, Mian Muhammad, Ullah, Farhad
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.08.2019
Subjects
Animals
Antioxidant
Buffalo spermatozoa
Buffaloes - physiology
Cryopreservation - veterinary
Fertility
Male
Motility
Plasma membrane integrity
Quercetin
Quercetin - pharmacology
Semen Analysis - veterinary
Semen Preservation - veterinary
Spermatozoa - drug effects
Spermatozoa - physiology
Buffalo spermatozoa
Motility
Antioxidant
Fertility
Plasma membrane integrity
Quercetin
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Abstract Aim of this study was to evaluate the stimulating effects of quercetin (QUE) on post thaw quality and in vivo fertility of buffalo (Bubalus bubalis) bull spermatozoa. QUE is a well-known flavonoid having antioxidant properties to scavenge free radicals. Semen was collected from three buffalo bull through artificial vagina (42 °C) and were evaluated initially for volume, motility, concentration, followed by dilution in five extenders (n = 5 aliquots, control, C = no QUE; treatment 1, T1 = 50 μM QUE; treatment 2, T2 = 100 μM QUE; treatment 3, T3 = 150 μM QUE and treatment 4, T4 = 200 μM QUE supplementation). The experiment was repeated thrice (n = 3 replicates). At post dilution, sperm progressive motility (PM, %) plasma membrane integrity (PMI, %), supra vital plasma membrane integrity (SVPMI, %) and acrosome integrity (ACR-1, %) of buffalo bull were significantly higher (P < 0.05) in extenders supplemented with QUE than C. At thawing, sperm PM of buffalo bull was higher in T3 and T4 than C, T1 and T2. Sperm SVPMI was significantly higher in T2, T3 and T4 than C and T1. Sperm ACR-I was higher in T3 and T4 than C, T1 and T2. Sperm DNA integrity was higher in T4 than C. QUE supplementation increased in vitro semen quality during 30 and 60 min of incubation at 37 °C than C. The in vivo fertility was higher in T3 and T4 than C (%, 61.82 vs. 65.22 vs. 46.90). It is concluded that QUE @ 150 and 200 μM improved post thaw semen quality and in vivo fertility of buffalo bull. •The present study was designed to assess the stimulating effects of Quercetin (QUE) in tris citric acid extender on post thaw quality and in vivo fertility of buffalo bull spermatozoa.•Inclusion of Quercetin improves semen quality in terms of progressive motility, plasma membrane, supra vital plasma membrane, acrosome and DNA integrities of buffalo bull spermatozoa.•The present study revealed that inclusion of Quercetin improves the in vivo fertility of buffalo bull spermatozoa.
AbstractList Aim of this study was to evaluate the stimulating effects of quercetin (QUE) on post thaw quality and in vivo fertility of buffalo (Bubalus bubalis) bull spermatozoa. QUE is a well-known flavonoid having antioxidant properties to scavenge free radicals. Semen was collected from three buffalo bull through artificial vagina (42 °C) and were evaluated initially for volume, motility, concentration, followed by dilution in five extenders (n = 5 aliquots, control, C = no QUE; treatment 1, T1 = 50 μM QUE; treatment 2, T2 = 100 μM QUE; treatment 3, T3 = 150 μM QUE and treatment 4, T4 = 200 μM QUE supplementation). The experiment was repeated thrice (n = 3 replicates). At post dilution, sperm progressive motility (PM, %) plasma membrane integrity (PMI, %), supra vital plasma membrane integrity (SVPMI, %) and acrosome integrity (ACR-1, %) of buffalo bull were significantly higher (P < 0.05) in extenders supplemented with QUE than C. At thawing, sperm PM of buffalo bull was higher in T3 and T4 than C, T1 and T2. Sperm SVPMI was significantly higher in T2, T3 and T4 than C and T1. Sperm ACR-I was higher in T3 and T4 than C, T1 and T2. Sperm DNA integrity was higher in T4 than C. QUE supplementation increased in vitro semen quality during 30 and 60 min of incubation at 37 °C than C. The in vivo fertility was higher in T3 and T4 than C (%, 61.82 vs. 65.22 vs. 46.90). It is concluded that QUE @ 150 and 200 μM improved post thaw semen quality and in vivo fertility of buffalo bull. •The present study was designed to assess the stimulating effects of Quercetin (QUE) in tris citric acid extender on post thaw quality and in vivo fertility of buffalo bull spermatozoa.•Inclusion of Quercetin improves semen quality in terms of progressive motility, plasma membrane, supra vital plasma membrane, acrosome and DNA integrities of buffalo bull spermatozoa.•The present study revealed that inclusion of Quercetin improves the in vivo fertility of buffalo bull spermatozoa.
Aim of this study was to evaluate the stimulating effects of quercetin (QUE) on post thaw quality and in vivo fertility of buffalo (Bubalus bubalis) bull spermatozoa. QUE is a well-known flavonoid having antioxidant properties to scavenge free radicals. Semen was collected from three buffalo bull through artificial vagina (42 °C) and were evaluated initially for volume, motility, concentration, followed by dilution in five extenders (n = 5 aliquots, control, C = no QUE; treatment 1, T1 = 50 μM QUE; treatment 2, T2 = 100 μM QUE; treatment 3, T3 = 150 μM QUE and treatment 4, T4 = 200 μM QUE supplementation). The experiment was repeated thrice (n = 3 replicates). At post dilution, sperm progressive motility (PM, %) plasma membrane integrity (PMI, %), supra vital plasma membrane integrity (SVPMI, %) and acrosome integrity (ACR-1, %) of buffalo bull were significantly higher (P < 0.05) in extenders supplemented with QUE than C. At thawing, sperm PM of buffalo bull was higher in T3 and T4 than C, T1 and T2. Sperm SVPMI was significantly higher in T2, T3 and T4 than C and T1. Sperm ACR-I was higher in T3 and T4 than C, T1 and T2. Sperm DNA integrity was higher in T4 than C. QUE supplementation increased in vitro semen quality during 30 and 60 min of incubation at 37 °C than C. The in vivo fertility was higher in T3 and T4 than C (%, 61.82 vs. 65.22 vs. 46.90). It is concluded that QUE @ 150 and 200 μM improved post thaw semen quality and in vivo fertility of buffalo bull.
Author Salman, Mian Muhammad
Ahmed, Hussain
Jahan, Sarwat
Ullah, Farhad
Author_xml – sequence: 1
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  surname: Ahmed
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– sequence: 2
  givenname: Sarwat
  surname: Jahan
  fullname: Jahan, Sarwat
  organization: Reproductive Physiology Laboratory, Department of Animal Sciences, Quaid-i-Azam University, Islamabad, Pakistan
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  givenname: Mian Muhammad
  surname: Salman
  fullname: Salman, Mian Muhammad
  organization: College of Animal Husbandry & Veterinary Sciences, Abdul Wali Khan University, Mardan, Pakistan
– sequence: 4
  givenname: Farhad
  surname: Ullah
  fullname: Ullah, Farhad
  organization: Department of Zoology, Islamia College University, Peshawar, Khyber Pakhtunkhwa (KP), Pakistan
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Keywords Buffalo spermatozoa
Motility
Antioxidant
Fertility
Plasma membrane integrity
Quercetin
Language English
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Snippet Aim of this study was to evaluate the stimulating effects of quercetin (QUE) on post thaw quality and in vivo fertility of buffalo (Bubalus bubalis) bull...
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SubjectTerms Animals
Antioxidant
Buffalo spermatozoa
Buffaloes - physiology
Cryopreservation - veterinary
Fertility
Male
Motility
Plasma membrane integrity
Quercetin
Quercetin - pharmacology
Semen Analysis - veterinary
Semen Preservation - veterinary
Spermatozoa - drug effects
Spermatozoa - physiology
Title Stimulating effects of Quercetin (QUE) in tris citric acid extender on post thaw quality and in vivo fertility of buffalo (Bubalus bubalis) bull spermatozoa
URI https://dx.doi.org/10.1016/j.theriogenology.2019.05.012
https://www.ncbi.nlm.nih.gov/pubmed/31112913
https://search.proquest.com/docview/2231846797
Volume 134
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