|
|
||||||||
Regular Article |
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.
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:
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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 |