“…Substitution of amino acids also modified polarity and tertiary structure of the GnRHa, which results in an improvement receptor binding affinity (Zohar and Mylonas, 2001). The unsatisfactory potency of natural GnRH peptides was improved by synthesising a superactive GnRHa, which is able to induce a significant increase in LH levels even at centuple smaller doses than with the use of natural GnRH forms (Table 1), (Kouril et al, 1986(Kouril et al, , 2007. The range of effective doses of GnRHa varies from 5-100 μg/kg and in the case of DI from 5-20 mg/kg of effective matter (Kouril et al, 1986;Drori et al, 1994;Brzuska, 1999;Szabo et al, 2002;Glasser et al, 2004;Mikolajczyk et al, 2004;Rutaisire and Booth, 2004;Kucharcyzk et al, 2005;Heyrati et al, 2007 Due to the strong dopaminergic inhibition of LH secretion, typical for the family Cyprinidae, a majority of trials with ovulation induction using only GnRHa failed (Weil et al, 1980;Sokolowska et al, 1984).…”