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Theriogenology2018; 119; 10-17; doi: 10.1016/j.theriogenology.2018.06.016

Carnosine as malondialdehyde scavenger in stallion seminal plasma and its role in sperm function and oxidative status.

Abstract: Semen biotechniques may impair sperm quality due to excessive production of reactive oxygen species (ROS). Additionally, products of the oxidative reaction, especially involving lipids (e.g., malondialdehyde - MDA), may be even more harmful to sperm. Carnosine, previously reported to be present in seminal plasma of several species, may be a key factor on sperm tolerance to biotechniques by counterattacking the deleterious influence of MDA. Therefore, the aim of this study was to measure the levels of carnosine present in equine seminal plasma and relate these findings with sperm function and oxidative status during cooling and cryopreservation. Thus, semen samples were collected from 40 stallions in duplicate (N = 80) and then submitted to cooling and cryopreservation. Samples were then allocated into groups of high and low tolerance to refrigeration and cryopreservation (bad cooler and good cooler/bad freezer and good freezer, respectively), and in groups of different concentrations of carnosine (High, Medium-high, Medium-low and Low carnosine). Samples were evaluated for sperm kinetics patterns, function of sperm structures and oxidative status. In good cooler samples, it was observed higher concentrations of carnosine (Good cooler: 224.98 ± 19.16 ng/mL; Bad cooler: 159.72 ± 15.99 ng/mL; p = 0.0056), ROS production (Good cooler: 26.40 ± 18.33%; Bad cooler: 18.33 ± 1.84%; p = 0.001) and lipid peroxidation rates (Good cooler: 193.23 ± 18.22 ng/mL; Bad cooler: 131.92 ± 12.25; p = 0.0064). Groups of samples with higher carnosine concentrations had lower levels of malondialdehyde (High: 79.33 ± 6.72 ng/mL; Medium-high: 140.45 ± 11.70 ng/mL; Medium-low: 202.57 ± 16.30 ng/mL and Low: 231.02 ± 32.35 ng/mL; p < 0.05), demonstrating that carnosine was effective in removing lipid peroxidation products. Due to the removal of seminal plasma during the cryopreservation process, no differences occurred in carnosine levels between bad and good freezer groups. In this context, this study provides relevant data for future therapies using carnosine during cryopreservation, aiming to replace the levels lost due to the necessary removal of seminal plasma.
Publication Date: 2018-06-23 PubMed ID: 29960162DOI: 10.1016/j.theriogenology.2018.06.016Google Scholar: Lookup
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  • Journal Article

Summary

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This research article investigates the role of Carnosine, an antioxidant present in seminal plasma, in preventing sperm damage during cooling and cryopreservation processes. The study also correlates Carnosine concentration with sperm function and oxidative status.

The Purpose and Methodology of the Study

  • The study was conducted with an aim to measure the Carnosine levels present in the seminal plasma of stallions (a male horse species) and examine how these levels affect sperm function and oxidative status during cooling and cryopreservation (a process of preserving biological constructs by cooling them to very low temperatures).
  • 80 semen samples were collected from 40 stallions and categorized into groups based on tolerance to refrigeration and cryopreservation, and concentrations of Carnosine.
  • Key Findings of the Research

    • The research identified that semen samples with higher Carnosine concentrations displayed better tolerance to refrigeration and lower rates of reactive oxygen species (ROS) production and lipid peroxidation (a process that damages cell membranes).
    • It also found that the higher the concentration of Carnosine in a sample, the lower the level of malondialdehyde (MDA), a potentially harmful by-product of lipid peroxidation.

    Importance of Carnosine

    • The study proves that Carnosine interacts directly with malondialdehyde, helping to neutralize its deleterious effects on sperm during cooling and cryopreservation.
    • Thus, Carnosine effectively aids in maintaining sperm health and function during these processes by combating oxidative stress and lipid peroxidation.

    Implications of the Findings

    • This study provides valuable insight for future research and therapies, suggesting that the levels of Carnosine may be replenished during cryopreservation to counteract the loss due to the removal of seminal plasma.

    Limitations of the Study

    • However, the study also indicates that during cryopreservation, there were no noticeable differences in Carnosine levels between semen samples showing good or bad tolerance to freezing. The reason for this is unclear and would need further examination.

Cite This Article

APA
Rocha CC, Kawai GKV, de Agostini Losano JD, Angrimani DSR, Rui BR, de Cássia Bicudo L, da Silva BDCS, Alonso MA, Mendes CM, Ortiz D'Avila Assumpção ME, Pereira RJG, Barnabe VH, Nichi M. (2018). Carnosine as malondialdehyde scavenger in stallion seminal plasma and its role in sperm function and oxidative status. Theriogenology, 119, 10-17. https://doi.org/10.1016/j.theriogenology.2018.06.016

Publication

ISSN: 1879-3231
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 119
Pages: 10-17
PII: S0093-691X(18)30381-9

Researcher Affiliations

Rocha, Carolina Camargo
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Kawai, Giulia Kiyomi Vechiato
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
de Agostini Losano, João Diego
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Angrimani, Daniel de Souza Ramos
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Rui, Bruno Rogério
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
de Cássia Bicudo, Luana
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
da Silva, Bárbara do Carmo Simões
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Alonso, Maria Augusta
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Mendes, Camilla Mota
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Ortiz D'Avila Assumpção, Mayra Elena
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Pereira, Ricardo José Garcia
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Barnabe, Valquíria Hyppolito
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil.
Nichi, Marcilio
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Orlando Marques de Paiva, 87, 05508-270, São Paulo, Brazil. Electronic address: mnichi@usp.br.

MeSH Terms

  • Animals
  • Antioxidants / chemistry
  • Antioxidants / pharmacology
  • Carnosine / chemistry
  • Carnosine / pharmacology
  • Cryopreservation / veterinary
  • Horses
  • Lipid Peroxidation
  • Male
  • Malondialdehyde / chemistry
  • Semen / chemistry
  • Semen Preservation / veterinary

Citations

This article has been cited 3 times.
  1. Dos Reis WVA, Pereira RR, Vieira M, da Cunha CCT, Acácio BR, Macedo GG, da Costa-E-Silva EV, Sampaio BFB. Impact of quercetin, carnosine, and ozone in the cryopreservation on Nellore (Bos indicus) semen. Anim Reprod 2023;20(1):e20220048.
    doi: 10.1590/1984-3143-AR2022-0048pubmed: 37034117google scholar: lookup
  2. Sarkar PK, Egusa A, Matsuzaki M, Sasanami T. Effect of Anserine and Carnosine on Sperm Motility in the Japanese Quail. J Poult Sci 2021;58(3):186-191.
    doi: 10.2141/jpsa.0200071pubmed: 34447283google scholar: lookup
  3. Gao J, Yang P, Cui Y, Meng Q, Feng Y, Hao Y, Liu J, Piao X, Gu X. Identification of Metabonomics Changes in Longissimus Dorsi Muscle of Finishing Pigs Following Heat Stress through LC-MS/MS-Based Metabonomics Method. Animals (Basel) 2020 Jan 13;10(1).
    doi: 10.3390/ani10010129pubmed: 31941143google scholar: lookup