Biol Reprod Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow My Folders
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Koshimoto, C.
Right arrow Articles by Mazur, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Koshimoto, C.
Right arrow Articles by Mazur, P.
Agricola
Right arrow Articles by Koshimoto, C.
Right arrow Articles by Mazur, P.
Biology of Reproduction 66, 1477-1484 (2002)
© 2002 Society for the Study of Reproduction, Inc.


Regular Article

Effects of Cooling and Warming Rate to and from -70°C, and Effect of Further Cooling from -70 to -196°C on the Motility of Mouse Spermatozoa1

Chihiro Koshimoto3,a, and Peter Mazur2,a

a Fundamental and Applied Cryobiology Group, Department of Biochemistry and Cellular and Molecular Biology, The University of Tennessee, Knoxville, Tennessee 37932-2575

We have previously reported high survival in mouse sperm frozen at 21°C/min to -70°C in a solution containing 18% raffinose in 0.25x PBS (400 mOsm) and then warmed rapidly at approximately 2000°C/min, especially under lowered oxygen tensions induced by Oxyrase, a bacterial membrane preparation. The best survival rates were obtained in the absence of glycerol. The first concern of the present study was to determine the effects of the cooling rate on the survival of sperm suspended in this medium. The sperm were cooled to -70°C at rates ranging from 0.3 to 530°C/min. The survival curve was an inverted "U" shape, with the highest motility occurring between 27 and 130°C/min. Survival decreased precipitously at higher cooling rates. Decreasing the warming rate, however, decreased survivals at all cooling rates. The motility depression with slow warming was especially evident in sperm cooled at the optimal rates. This fact is consistent with our current view that the frozen medium surrounding sperm cells is in a metastable state, perhaps partly vitrified as a result of the high concentrations of sugar. The decimation of sperm cooled more rapidly than optimum (>130°C/min), even with rapid warming, is consistent with the induction of considerable quantities of intracellular ice at these rates. When glycerol was added to the above medium, motilities were also dependent on the cooling rate, but they tended to be substantially lower than those obtained in the absence of glycerol. The minimum temperature in the above experiments was -70°C. When sperm were frozen to -70°C at optimum rates, lowering the temperature to -196°C had no adverse effect.

First decision: 1 November 2001.

1 Supported by NIH grant R24-RR13194 (J. Critser, PI) under subcontract with Indiana University. A preliminary report was presented at the 37th Annual Meeting of the Society of Cryobiology; Cambridge, MA; 30 July to 1 August 2000.

2 Correspondence: Peter Mazur, Fundamental and Applied Cryobiology Group, Dept. of Biochemistry and Cellular and Molecular Biology, The University of Tennessee, 10515 Research Dr., Suite 300/10, Knoxville, TN 37932-2575. FAX: 865 974 8027; pmazur{at}utk.edu

3 Current address: Experimental Animal Center, 5200 Miyazaki Medical College, Kiyotake, Miyazaki 889-1692, Japan




This article has been cited by other articles:


Home page
Biol. Reprod.Home page
P. Mazur, S.P Leibo, and G. E Seidel Jr.
Cryopreservation of the Germplasm of Animals Used in Biological and Medical Research: Importance, Impact, Status, and Future Directions
Biol Reprod, January 1, 2008; 78(1): 2 - 12.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
Y. Yamauchi, A. Ajduk, J. M Riel, and M. A Ward
Ejaculated and Epididymal Mouse Spermatozoa Are Different in Their Susceptibility to Nuclease-Dependent DNA Damage and in Their Nuclease Activity
Biol Reprod, October 1, 2007; 77(4): 636 - 647.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
F. Fonseca, M. Marin, and G. J. Morris
Stabilization of Frozen Lactobacillus delbrueckii subsp. bulgaricus in Glycerol Suspensions: Freezing Kinetics and Storage Temperature Effects.
Appl. Envir. Microbiol., October 1, 2006; 72(10): 6474 - 6482.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
A. Ajduk, Y. Yamauchi, and M. A Ward
Sperm Chromatin Remodeling after Intracytoplasmic Sperm Injection Differs from That of In Vitro Fertilization
Biol Reprod, September 1, 2006; 75(3): 442 - 451.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
V. Frederickx, A. Michiels, E. Goossens, G. De Block, A.C. Van Steirteghem, and H. Tournaye
Recovery, survival and functional evaluation by transplantation of frozen-thawed mouse germ cells
Hum. Reprod., April 1, 2004; 19(4): 948 - 953.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
M. A. Ward, T. Kaneko, H. Kusakabe, J. D. Biggers, D. G. Whittingham, and R. Yanagimachi
Long-Term Preservation of Mouse Spermatozoa after Freeze-Drying and Freezing Without Cryoprotection
Biol Reprod, December 1, 2003; 69(6): 2100 - 2108.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
P. Mazur and C. Koshimoto
Is Intracellular Ice Formation the Cause of Death of Mouse Sperm Frozen at High Cooling Rates?
Biol Reprod, May 1, 2002; 66(5): 1485 - 1490.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 by the Society for the Study of Reproduction.