Dimethyl sulfoxide perfusion in caprine ovarian tissue and its relationship with follicular viability after cryopreservation Valesca B. Luz, D.V.M., Regiane R. Santos, Ph.D., Leonardo C. Pinto, D.V.M., Alison A.X. Soares, D.V.M., Juliana J.H. Celestino, M.S., Jair Mafezoli, Ph.D., Cláudio C. Campello, Ph.D., José R. Figueiredo, Ph.D., Ana P.R. Rodrigues, Ph.D. Fertility and Sterility Volume 91, Issue 4, Pages 1513-1515 (April 2009) DOI: 10.1016/j.fertnstert.2008.07.1778 Copyright © 2009 American Society for Reproductive Medicine Terms and Conditions
Figure 1 Percentage (mean ± SD) of (A) morphologically normal early-stage follicles after exposure to dimethyl sulfoxide (DMSO), (B) DMSO perfusion (mg) into the ovarian tissue after exposure and (C) viable follicles after cryopreservation. ∗Statistically significant difference from control. a,bStatistically significant difference among incubation times (10, 20, 30, and 40 minutes). A,BStatistically significant difference among DMSO concentrations (1.0, 1.5, and 2.0 M). Fertility and Sterility 2009 91, 1513-1515DOI: (10.1016/j.fertnstert.2008.07.1778) Copyright © 2009 American Society for Reproductive Medicine Terms and Conditions