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The antioxidant system of seminal fluid during in vitro storage of sterlet Acipenser ruthenus sperm.

Identifieur interne : 000025 ( Main/Curation ); précédent : 000024; suivant : 000026

The antioxidant system of seminal fluid during in vitro storage of sterlet Acipenser ruthenus sperm.

Auteurs : Viktoriya Dzyuba [République tchèque] ; Jacky Cosson [République tchèque] ; Borys Dzyuba [République tchèque] ; Gunes Yamaner [Turquie] ; Marek Rodina [République tchèque] ; Otomar Linhart [République tchèque]

Source :

Fish physiology and biochemistry [ 1573-5168 ] ; 2016.

RBID : pubmed:26559692

English descriptors

KwdEn :
- Animals, Catalase (metabolism), Fishes (physiology), Male, Oxidative Stress, Semen (metabolism), Sperm Motility, Spermatozoa, Superoxide Dismutase (metabolism), Thiobarbituric Acid Reactive Substances (metabolism), Uric Acid.
MESH :
- chemical , metabolism : Catalase, Superoxide Dismutase, Thiobarbituric Acid Reactive Substances.
- metabolism : Semen.
- physiology : Fishes.
- Animals, Male, Oxidative Stress, Sperm Motility, Spermatozoa, Uric Acid.

Abstract

The role of the seminal fluid antioxidant system in protection against damage to spermatozoa during in vitro sperm storage is unclear. This study investigated the effect of in vitro storage of sterlet Acipenser ruthenus spermatozoa together with seminal fluid for 36 h at 4 °C on spermatozoon motility rate and curvilinear velocity, thiobarbituric acid reactive substance level, and components of enzyme and non-enzyme antioxidant system (superoxide dismutase and catalase activity and uric acid concentration) in seminal fluid. Spermatozoon motility parameters after sperm storage were significantly decreased, while the level of thiobarbituric acid reactive substances, activity of superoxide dismutase and catalase, and uric acid concentration did not change. Our findings suggest that the antioxidant system of sterlet seminal fluid is effective in preventing oxidative stress during short-term sperm storage and prompt future investigations of changes in spermatozoon homeostasis and in spermatozoon plasma membrane structure which are other possible reasons of spermatozoon motility deterioration upon sperm storage.

DOI: 10.1007/s10695-015-0159-1
PubMed: 26559692

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Le document en format XML

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<term>Semen (metabolism)</term>
<term>Sperm Motility</term>
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<term>Superoxide Dismutase (metabolism)</term>
<term>Thiobarbituric Acid Reactive Substances (metabolism)</term>
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<term>Superoxide Dismutase</term>
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<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
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<term>Oxidative Stress</term>
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<front><div type="abstract" xml:lang="en">The role of the seminal fluid antioxidant system in protection against damage to spermatozoa during in vitro sperm storage is unclear. This study investigated the effect of in vitro storage of sterlet Acipenser ruthenus spermatozoa together with seminal fluid for 36 h at 4 °C on spermatozoon motility rate and curvilinear velocity, thiobarbituric acid reactive substance level, and components of enzyme and non-enzyme antioxidant system (superoxide dismutase and catalase activity and uric acid concentration) in seminal fluid. Spermatozoon motility parameters after sperm storage were significantly decreased, while the level of thiobarbituric acid reactive substances, activity of superoxide dismutase and catalase, and uric acid concentration did not change. Our findings suggest that the antioxidant system of sterlet seminal fluid is effective in preventing oxidative stress during short-term sperm storage and prompt future investigations of changes in spermatozoon homeostasis and in spermatozoon plasma membrane structure which are other possible reasons of spermatozoon motility deterioration upon sperm storage.</div>
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The antioxidant system of seminal fluid during in vitro storage of sterlet Acipenser ruthenus sperm.

The antioxidant system of seminal fluid during in vitro storage of sterlet Acipenser ruthenus sperm.

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English descriptors

Abstract

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