1.Excess of leptin inhibits hypothalamic KiSS-1 expression in pubertal mice.
Sung Yeon AHN ; Sei Won YANG ; Hee Jae LEE ; Jong Seon BYUN ; Ji Yeon OM ; Choong Ho SHIN
Korean Journal of Pediatrics 2012;55(9):337-343
PURPOSE: Leptin has been considered a link between metabolic state and reproductive activity. Defective reproductive function can occur in leptin-deficient and leptin-excessive conditions. The aim of this study was to examine the effects of centrally injected leptin on the hypothalamic KiSS-1 system in relation to gonadotropin-releasing hormone (GnRH) action in the initial stage of puberty. METHODS: Leptin (1 microg) was injected directly into the ventricle of pubertal female mice. The resultant gene expressions of hypothalamic GnRH and KiSS-1 and pituitary LH, 2 and 4 hours after injection, were compared with those of saline-injected control mice. The changes in the gene expressions after blocking the GnRH action were also analyzed. RESULTS: The basal expression levels of KiSS-1, GnRH, and LH were significantly higher in the pubertal mice than in the prepubertal mice. The 1-microg leptin dose significantly decreased the mRNA expression levels of KiSS-1, GnRH, and LH in the pubertal mice. A GnRH antagonist significantly increased the KiSS-1 and GnRH mRNA expression levels, and the additional leptin injection decreased the gene expression levels compared with those in the control group. CONCLUSION: The excess leptin might have suppressed the central reproductive axis in the pubertal mice by inhibiting the KiSS-1 expression, and this mechanism is independent of the GnRH-LH-estradiol feedback loop.
Aluminum Hydroxide
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Animals
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Axis, Cervical Vertebra
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Carbonates
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Female
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Gene Expression
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Gonadotropin-Releasing Hormone
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Humans
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Leptin
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Luteinizing Hormone
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Mice
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Puberty
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RNA, Messenger