Exploring the effect of cold stress on the semen quality parameters of buffalo bulls

The objective of the current study was to evaluate how buffalo bulls’ semen quality is affected by cold stress. A total of 26 adult Murrah buffaloes were taken at the Artificial Breeding Research Centre, ICAR-National Dairy Research Institute, Karnal, India. Semen collection of these bulls was done...

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Main Authors: Karpenahalli Ranganatha Sriranga, Pawan Singh, Ravinder Singh, Tejeshwari Satpute, Prince Vivek, Tushar Kumar Mohanty, Pradeep Kumar, Ranjit Singh Kataria, Megha Pande, Manishi Mukesh
Format: Article
Language:English
Published: Universidad del Zulia 2023-11-01
Series:Revista Científica
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Online Access:https://www.produccioncientificaluz.org/index.php/cientifica/article/view/43445
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author Karpenahalli Ranganatha Sriranga
Pawan Singh
Ravinder Singh
Tejeshwari Satpute
Prince Vivek
Tushar Kumar Mohanty
Pradeep Kumar
Ranjit Singh Kataria
Megha Pande
Manishi Mukesh
author_facet Karpenahalli Ranganatha Sriranga
Pawan Singh
Ravinder Singh
Tejeshwari Satpute
Prince Vivek
Tushar Kumar Mohanty
Pradeep Kumar
Ranjit Singh Kataria
Megha Pande
Manishi Mukesh
author_sort Karpenahalli Ranganatha Sriranga
collection DOAJ
description The objective of the current study was to evaluate how buffalo bulls’ semen quality is affected by cold stress. A total of 26 adult Murrah buffaloes were taken at the Artificial Breeding Research Centre, ICAR-National Dairy Research Institute, Karnal, India. Semen collection of these bulls was done twice during the peak of winter and spring seasons with overall average ambient temperature (°C) of 12.55±0.22 and 20.21±0.68, respectively, and blood was collected on the same day for biochemical analysis. Routine seminal attributes, viz., semen volume, sperm concentration, mass activity, individual motility, viability, acrosome integrity, and hypo-osmotic swelling test (HOST), were evaluated immediately after semen collection, and diluted semen was cryopreserved for further studies. Additionally, fresh and frozen sperm were subjected to flow cytometric analysis utilizing the Luminex MUSE Cell Analyzer and CytoFLEX, Beckman Coulter-Life Sciences, respectively. Sperm motility characteristics were assessed using a CASA (Hamilton Thorne IVOS II) with the help of eight chambered Leja slides. Further, serum hormones were assayed through the CMIA technique, and the antioxidant status of both serum and seminal plasma was done using standard protocol. Statistical analyses were performed using IBM SPSS Statistics software (v.20.0). The THI during the winter and spring seasons was 54.85±0.38 (THI range; 40.93 – 60.38) and 66.89±1.03 (THI range; 60.04 – 77.99), respectively, while the cold stress index was 857.62±8.89 and 793.08±14.10, respectively, demonstrating that the values varied significantly between the seasons (p=0.001). Fresh seminal attributes such as volume (2.86±0.20 vs. 2.73±0.15 ml, p=0.616), concentration (1181.94±71.32 vs. 1115.10±78.34 x 106/ml, p=0.529), mass activity (2.28±0.09 vs. 2.47±0.08, p=0.094), viability (81.95±1.07 vs. 82.13±0.89%, p=0.896), and acrosome integrity (86.17±0.86 vs. 87.53±0.75%, p=0.239), did not vary between the extreme winter and comfortable spring seasons. However, individual motility, HOST (66.75±1.41 vs. 71.13±1.25%, p=0.022), and discard rate (48.36±1.92 vs 36.44±5.51%, p=0.024) of semen were affected by cold stress. ROS (+) cells and apoptotic cells in fresh semen were not affected by cold stress, despite their higher values in the winter season. A similar trend was observed with MitoSOX (+) cells and live acrosome intact cells in frozen semen. Further, cold stress had a significant influence on the sperm kinematic characteristics of both fresh and frozen-thawed semen. Serum hormones such as Triiodothyronine (5.23±0.16 vs. 4.41±0.14 ng/mL, p=0.000), testosterone (0.99±0.12 vs. 1.68±0.17 ng/mL, p=0.002), cortisol (3.66±0.43 vs 2.29±0.12 ng/mL, p=0.004), and LDH (1078.54±12.32 vs 988.23±13.54 U/L, p=0.000) were affected by the cold weather. In addition, GSH and MDA concentrations in both seminal plasma and serum were affected by cold stress. In conclusion, frigid temperatures also contribute as a stress factor, further leading to a significant reduction in the semen quality of buffalo bulls.
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spelling doaj-art-f7ef41e06ba243f88dd63bc6aa219c222025-02-03T15:37:02ZengUniversidad del ZuliaRevista Científica0798-22592521-97152023-11-0133Suplemento10.52973/rcfcv-wbc101Exploring the effect of cold stress on the semen quality parameters of buffalo bullsKarpenahalli Ranganatha Sriranga0Pawan Singh1Ravinder Singh2Tejeshwari Satpute3Prince Vivek 4Tushar Kumar Mohanty5Pradeep Kumar6Ranjit Singh Kataria7Megha Pande 8Manishi Mukesh9 Livestock Production Management Division, ICAR-National Dairy Research Institute, Karnal, India.Livestock Production Management Division, ICAR-National Dairy Research Institute, Karnal, India. Livestock Production Management Division, ICAR-National Dairy Research Institute, Karnal, India.Livestock Production Management Division, ICAR-National Dairy Research Institute, Karnal, India.Livestock Production Management Division, ICAR-National Dairy Research Institute, Karnal, India. Livestock Production Management Division, ICAR-National Dairy Research Institute, Karnal, India.Division of Animal Physiology & Reproduction, ICAR-Central Institute for Research on Buffaloes, Hisar, India.Animal Biotechnology, ICAR-National Bureau of Animal Genetic Resources, Karnal, India.Division of Cattle Physiology & Reproduction, ICAR- Central Institute for Research on Cattle, Meerut, IndiaAnimal Biotechnology, ICAR-National Bureau of Animal Genetic Resources, Karnal, India. The objective of the current study was to evaluate how buffalo bulls’ semen quality is affected by cold stress. A total of 26 adult Murrah buffaloes were taken at the Artificial Breeding Research Centre, ICAR-National Dairy Research Institute, Karnal, India. Semen collection of these bulls was done twice during the peak of winter and spring seasons with overall average ambient temperature (°C) of 12.55±0.22 and 20.21±0.68, respectively, and blood was collected on the same day for biochemical analysis. Routine seminal attributes, viz., semen volume, sperm concentration, mass activity, individual motility, viability, acrosome integrity, and hypo-osmotic swelling test (HOST), were evaluated immediately after semen collection, and diluted semen was cryopreserved for further studies. Additionally, fresh and frozen sperm were subjected to flow cytometric analysis utilizing the Luminex MUSE Cell Analyzer and CytoFLEX, Beckman Coulter-Life Sciences, respectively. Sperm motility characteristics were assessed using a CASA (Hamilton Thorne IVOS II) with the help of eight chambered Leja slides. Further, serum hormones were assayed through the CMIA technique, and the antioxidant status of both serum and seminal plasma was done using standard protocol. Statistical analyses were performed using IBM SPSS Statistics software (v.20.0). The THI during the winter and spring seasons was 54.85±0.38 (THI range; 40.93 – 60.38) and 66.89±1.03 (THI range; 60.04 – 77.99), respectively, while the cold stress index was 857.62±8.89 and 793.08±14.10, respectively, demonstrating that the values varied significantly between the seasons (p=0.001). Fresh seminal attributes such as volume (2.86±0.20 vs. 2.73±0.15 ml, p=0.616), concentration (1181.94±71.32 vs. 1115.10±78.34 x 106/ml, p=0.529), mass activity (2.28±0.09 vs. 2.47±0.08, p=0.094), viability (81.95±1.07 vs. 82.13±0.89%, p=0.896), and acrosome integrity (86.17±0.86 vs. 87.53±0.75%, p=0.239), did not vary between the extreme winter and comfortable spring seasons. However, individual motility, HOST (66.75±1.41 vs. 71.13±1.25%, p=0.022), and discard rate (48.36±1.92 vs 36.44±5.51%, p=0.024) of semen were affected by cold stress. ROS (+) cells and apoptotic cells in fresh semen were not affected by cold stress, despite their higher values in the winter season. A similar trend was observed with MitoSOX (+) cells and live acrosome intact cells in frozen semen. Further, cold stress had a significant influence on the sperm kinematic characteristics of both fresh and frozen-thawed semen. Serum hormones such as Triiodothyronine (5.23±0.16 vs. 4.41±0.14 ng/mL, p=0.000), testosterone (0.99±0.12 vs. 1.68±0.17 ng/mL, p=0.002), cortisol (3.66±0.43 vs 2.29±0.12 ng/mL, p=0.004), and LDH (1078.54±12.32 vs 988.23±13.54 U/L, p=0.000) were affected by the cold weather. In addition, GSH and MDA concentrations in both seminal plasma and serum were affected by cold stress. In conclusion, frigid temperatures also contribute as a stress factor, further leading to a significant reduction in the semen quality of buffalo bulls. https://www.produccioncientificaluz.org/index.php/cientifica/article/view/43445buffalo bullscold stressCASAflow cytometrysemen quality
spellingShingle Karpenahalli Ranganatha Sriranga
Pawan Singh
Ravinder Singh
Tejeshwari Satpute
Prince Vivek
Tushar Kumar Mohanty
Pradeep Kumar
Ranjit Singh Kataria
Megha Pande
Manishi Mukesh
Exploring the effect of cold stress on the semen quality parameters of buffalo bulls
Revista Científica
buffalo bulls
cold stress
CASA
flow cytometry
semen quality
title Exploring the effect of cold stress on the semen quality parameters of buffalo bulls
title_full Exploring the effect of cold stress on the semen quality parameters of buffalo bulls
title_fullStr Exploring the effect of cold stress on the semen quality parameters of buffalo bulls
title_full_unstemmed Exploring the effect of cold stress on the semen quality parameters of buffalo bulls
title_short Exploring the effect of cold stress on the semen quality parameters of buffalo bulls
title_sort exploring the effect of cold stress on the semen quality parameters of buffalo bulls
topic buffalo bulls
cold stress
CASA
flow cytometry
semen quality
url https://www.produccioncientificaluz.org/index.php/cientifica/article/view/43445
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