T. Sankai et al., IN-VITRO FERTILIZATION USING JAPANESE MON KEY (MACACA-FUSCATA) EGGS AND CYNOMOLGUS MONKEY (MACACA-FASCICULARIS) FROZEN THAWED SPERMATOZOA/, Jikken Dobutsu, 43(1), 1994, pp. 45-50
Using four female Japanese monkeys, follicular growth was induced by m
ultiple PMSG and single hCG injections, and oocytes were collected fro
m their follicles. PMSG, 200 IU, was injected six or eight times to st
imulate follicular growth, and in both cases growth of the follicles w
as adequately induced. Forty-seven (50.0%) oocytes were recovered from
94 follicles of two of the females and transported from Inuyama-shi t
o Tsukuba-shi in 10 hours. Five mature oocytes and 42 immature oocytes
were observed upon arrival. Thirteen (31.0%) of the 42 immature oocyt
es released the first polar body in TCM-199 medium containing FCS and
PMSG after 24 hour-culture, including transport time. Eighteen mature
oocytes were used for in vitro fertilization (IVF). Frozen and thawed
cynomolgus monkey spermatozoa preincubated for 2 hours were transferre
d into the drops containing the Japanese monkey oocytes. Sixteen oocyt
es (88.9%) were judged to have been success fully fertilized based on
the presence of a male pronucleus and/or second polar body, and 12 ooc
ytes then cleaved, and 3 developed into the 6-cell stage. Thus, we suc
ceeded in inducing follicular growth and oocyte maturation, and in ach
ieving IVF using cynomolgus monkey spermatozoa and Japanese monkey ooc
ytes.