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REVIEW: Current Status of Extenders and Cryoprotectants onFish Spermatozoa Cryopreservation

Zainal A. Muchlisin
- 01 Jan 2005 - 
- Vol. 6, Iss: 1, pp 66-69
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TLDR
A review of studies on the cryopreservation of mammalian sperm, animal husbandry sperm and human sperm have progressed significantly but studies on fish sperm is still confined to some aquatic.
Abstract
An important component of many studies of cryopreservation of fish spermatozoa is the type of extenders and cryoprotectants. The suitability of extenders and cryoprotectants differs from one fish to another. There are many studies have been done in cryopreservation of fish spermatozoa. However, there are few review have been done. This review reveals some aspects of cryopreservation especially the role of extender and cryoprotectant in fish sperm cryopreservation. Fish produce high viscosity of sperm and in some cases only small volume is produced. Before cryopreserved in liquid nitrogen, sperm have to dilute with extenders and for long-term cryopreservation,cryoprotectants are needed to protect the sperm cell from cold and hot shock treatments and prevent cell dehydration during pre-freezing, freezing and post thawed. The suitability of extenders and cryoprotectants differs from one fish to another. Over the last decade, studies on the cryopreservation of mammalian sperm, animal husbandry sperm and human sperm have progressed significantly but studies on fish sperm is still confined to some aquatic.© 2005 Jurusan Biologi FMIPA UNS SurakartaKey words: fish, sperm, cryopreservation, extenders, cryoprotectants

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Citations
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Journal ArticleDOI

Effect of seminal plasma on Atlantic salmon (Salmo salar) sperm vitrification.

TL;DR: This study was designed to test a vitrification method in Atlantic salmon spermatozoa and determine the capacity of seminal plasma (SP) to protect these cells from cryoinjuries.
Journal ArticleDOI

Cryopreservation of Atlantic salmon Salmo salar sperm: effects on sperm physiology

TL;DR: There were significant differences in the plasma membrane integrity, mitochondrial membrane potential, motility, fertilization rate, VCL, VAP and VSL compared with the controls (P < 0·05).
Journal ArticleDOI

Cryopreservation of sperm in farmed Australian greenlip abalone Haliotis laevigata.

TL;DR: A positive role of glucose in the improvement of sperm cryopreservation in farmed greenlip abalone is demonstrated, showing that the addition of glucose could significantly improve the sperm plasma membrane integrity and mitochondrial membrane potential.
Journal ArticleDOI

Influence of cryoprotectants on abnormality and motility of baung (Mystus nemurus) spermatozoa after long-term cryopreservation.

TL;DR: The effect of cryoprotectants on the spermatozoa abnormality and motility were significant and there is a negative correlation between sperm motility and abnormality.
Journal Article

Preliminary study on the natural extenders for artificial breeding of African catfish Clarias gariepinus (Burchell, 1822)

TL;DR: Coconut water showed the highest fertility and hatching rates at 1:20 dilution ratio and was the optimal condition for African catfish spermatozoa among the natural extenders investigated.
References
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Journal ArticleDOI

Cryopreservation of sperm from brown trout (Salmo trutta m. lacustris L.) and Arctic charr (Salvelinus alpinus L.)

Jorma Piironen
- 01 Oct 1993 - 
TL;DR: Cryopreservation of brown trout and Arctic charr sperm was studied by modifying sperm extenders and the amount of egg yolk (10 or 20%) as a protective component and glycerol proved to be better than DMSO for protection of Arcticcharr sperm.
Journal ArticleDOI

Cryopreservation of the sperm of the Japanese bitterling

TL;DR: Results indicate that 10% methanol plus 90% foetal bovine serum is a suitable diluent for cryopreservation of bitterling spermatozoa and that samples should be cooled to - 40°C at a low freezing rate for effective storage.
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Cryopreservation of sperm of common carp, Cyprinus carpio L.

TL;DR: Within the most effective treatments, survival from the eyed-egg stage to the swim-up stage was similar to that observed in the control group and was highly significantly and positively correlated with the actual rate of Swim-up larvae.
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Cryopreservation of Yellow Perch Semen

TL;DR: Two-year-old males were induced to spermiate 8–10 weeks before natural spawning by using an analog of luteinizing hormone releasing hormone (LHRH) to investigate methods for the cryopreservation of yellow perch (Perca flavescens) semen.
Journal ArticleDOI

Cryopreservation of Arctic charr, Salvelinus alpinus (L.), semen in various extenders and in three sizes of straw.

TL;DR: Fertility trials were conducted to determine the post-thaw viability of the frozen semen, and the motility of activated spermatozoa was higher in the DMA and DMSO extenders than in the glycerol extender.
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