Recent advances in knowledge of the endocrine and paracrine mechanisms that
regulate human ovarian folliculogenesis have been parallelled by the intro
duction into clinical practice of new drugs that can be used safely and eff
ectively to stimulate ovarian function in infertile women. Most notably, re
combinant DNA technology has been applied to the production of molecularly
pure forms of the gonadotrophins, FSH and LH, opening the way to the develo
pment of improved strategies for manipulating the ovarian paracrine system.
The clinical objectives of controlled ovarian stimulation fall into two ca
tegories, depending on patient needs: (1) induction of multiple follicles f
rom which mature oocytes can be harvested for use in assisted reproduction
protocols such as ill vitro fertilization and embryo transfer; or (2) induc
tion of spontaneous ovulation of a single mature follicle so that conceptio
n might occur in vivo. This review summarizes the physiological principles
upon which the use of gonadotrophins for clinical purposes is based, highli
ghting new opportunities for improved treatment as a result of the availabi
lity of recombinant FSH and LH.