60 YEARS OF NEUROENDOCRINOLOGY: The hypothalamo-prolactin axis

    1. David R Grattan1,2
    1. 1Centre for Neuroendocrinology and Department of Anatomy, University of Otago, PO Box 913, Dunedin 9054, New Zealand
      2Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand
    1. Correspondence should be addressed to D R Grattan; Email: dave.grattan{at}otago.ac.nz


    The hypothalamic control of prolactin secretion is different from other anterior pituitary hormones, in that it is predominantly inhibitory, by means of dopamine from the tuberoinfundibular dopamine neurons. In addition, prolactin does not have an endocrine target tissue, and therefore lacks the classical feedback pathway to regulate its secretion. Instead, it is regulated by short loop feedback, whereby prolactin itself acts in the brain to stimulate production of dopamine and thereby inhibit its own secretion. Finally, despite its relatively simple name, prolactin has a broad range of functions in the body, in addition to its defining role in promoting lactation. As such, the hypothalamo-prolactin axis has many characteristics that are quite distinct from other hypothalamo-pituitary systems. This review will provide a brief overview of our current understanding of the neuroendocrine control of prolactin secretion, in particular focusing on the plasticity evident in this system, which keeps prolactin secretion at low levels most of the time, but enables extended periods of hyperprolactinemia when necessary for lactation. Key prolactin functions beyond milk production will be discussed, particularly focusing on the role of prolactin in inducing adaptive responses in multiple different systems to facilitate lactation, and the consequences if prolactin action is impaired. A feature of this pleiotropic activity is that functions that may be adaptive in the lactating state might be maladaptive if prolactin levels are elevated inappropriately. Overall, my goal is to give a flavour of both the history and current state of the field of prolactin neuroendocrinology, and identify some exciting new areas of research development.

    • Received in final form 18 June 2015
    • Accepted 22 June 2015
    • Made available online as an Accepted Preprint 22 June 2015
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    This Article

    1. J Endocrinol 226 T101-T122
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