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  1. Helmy Mohd Mokhtar, Nelli Giribabu, Naguib Salleh
    Sains Malaysiana, 2018;47:2509-2517.
    Adequate development of uterine receptivity is crucial for establishment of pregnancy. Expression of uterine receptivity
    molecules i.e. αvβ3 integrin, E-cadherin and mucin-1 could be affected by testosterone. The objective of this study was
    to investigate effect of testosterone on expression of these molecules during early pregnancy. 30 ovariectomised female
    Sprague-Dawley rats were divided into 5 groups that consisted of vehicle control, rats received eight days sex-steroid
    replacement regime (intended to mimic the hormonal changes in early pregnancy) and three groups of rats given
    testosterone (1 mg/kg/day) subcutaneously with or without flutamide or finasteride between day 6 and 8 representing the
    period of uterine receptivity. At the end of the treatment, rats were sacrificed and uteri were removed. Expression and
    distribution of αvβ3 integrin, E-cadherin and mucin-1 were examined by immunoflourescence and levels of messenger
    RNA (mRNAs) were evaluated by real-time PCR. Expression of αvβ3 integrin, E-cadherin and mucin-1 in the uteri of
    rats receiving sex-steroid replacement regime increased significantly as compared to control (p<0.05). In these rats,
    concomitant administration of testosterone between day 6 and 8 resulted in expression of αvβ3 integrin, E-cadherin
    and mucin-1 to decrease significantly (p<0.05) as compared to rats receiving sex-steroid replacement regime without
    testosterone treatment. Moreover, the testosterone effects were not antagonized by either flutamide or finasteride. As
    a result, reduced expression of uterine receptivity molecules by testosterone might interfere with early pregnancy
    establishment, therefore could adversely affect the female fertility.
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