Abstract

The perinatal hormonal imprinting takes place perinatally, when the developing hormone receptors meet the hormones of the newborn and this suits the normal receptor-hormone connections for life. In this period the developmental window for imprinting is open and the receptors can be cheated by hormone-related exogeneous molecules, provoking faulty hormonal imprinting with lifelong consequences, as alteration of receptor binding capacity and hormone production, functional changes, altered sexual behavior, immunological alterations and inclination to or manifestation of diseases. However, there are other critical periods of life, when the window is open, as weaning, adolescence, regeneration in adults as well, as in continously dividing cells. The most sensitive non-perinatal critical period is the adolescence. In these periods hormone-like endocrine disruptors (e.g. bisphenol A, benzpyrene, pesticides and herbicides, soy isoflavones, medically used synthetic hormones etc) are provoking faulty hormonal imprinting with lifelong consequences. The hormonal imprinting is an epigenetic process, which is inherited to the progeny cells of the organism and to the offspring of the organism, by which it can chip in the evolution. The non-perinatal faulty hormonal imprinting is justified in animal experiments and seems to be likely in case of survivors of childhood cancer treatment. Similar to the faulty perinatal hormonal imprinting, the late (non-perinatal) faulty imprinting can participate in the provocation of later manifested diseases.

Highlights

  • The perinatal hormonal imprinting takes place perinatally, when the developing hormone receptors meet the hormones of the newborn and this suit the normal receptor-hormone connections for life

  • The facts clearly show that the perinatal physiological or faulty imprinting has a decisive role on the connection between the receptors and their target hormones, there are other critical periods when this connection could be deeply and durably influenced

  • This means that the developmental window is not definitively closed after the critical perinatal period, it is opened many times during life and this has physiological importance in some important life-processes

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Summary

Faulty hormonal imprinting during weaning

Weaned (25 day old) female rats were treated with endorphin, and endorphin and serotonin content were measured in adults. After single endorphin treatment of three-week old female rats serotonin content in five regions of the brain, sexual activity, uterine estrogen receptor binding were measured in adults. Retinol (vitamin A) or retinoic acid treatment of 6 or 7 weeks old male and female rats significantly influenced steroid hormone levels of the adult age [33]. Single vitamin D3 treatment of six weeks old male rat increased the thymic glucocorticoid receptor density of adult males [34]. The density of uterine estrogen receptors and thymic glucocorticoid receptors of adult female rats decreased after single adolescent treatment with the anabolic steroid nandrolone [35]. Eight weeks old rats were treated with serotonin and a radical reduction of serotonin content of male’s white blood cells (lymphocytes, monocytes, granulocytes) and mast cells were observed in adult age [39]. The isoflavone of soy given to prepubertal and adult periods protected against chemically induced mammary cancer [53]

Conclusion
Findings
Faulty hormonal imprinting in adults
Full Text
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