Α‐Melanocyte‐stimulating hormone inhibition of oxytocin neurons switches to excitation in late pregnancy and lactation. Issue 6 (21st March 2022)

• Record Type: Journal Article
• Authors: Perkinson, Michael R.; Kirchner, Matthew K.; Zhang, Meng; Augustine, Rachael A.; Stern, Javier E.; Brown, Colin H.
• Is Part Of: Physiological reports. Volume 10:Issue 6(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-03-21
• Subjects: lactation -- oxytocin -- pregnancy -- somato‐dendritic secretion -- vasopressin; Physiology -- Periodicals; 571
• DOI: 10.14814/phy2.15226
• Languages: English
• ISSNs: 2051-817X

Abstract

Abstract: Oxytocin is secreted into the periphery by magnocellular neurons of the hypothalamic supraoptic and paraventricular nuclei (SON and PVN) to trigger uterine contraction during birth and milk ejection during suckling. Peripheral oxytocin secretion is triggered by action potential firing, which is regulated by afferent input activity and by feedback from oxytocin secreted into the extracellular space from magnocellular neuron somata and dendrites. A prominent input to oxytocin neurons arises from proopiomelanocortin neurons of the hypothalamic arcuate nucleus that secrete an alpha‐melanocyte‐stimulating hormone (α‐MSH), which inhibits oxytocin neuron firing in non‐pregnant rats by increasing somato‐dendritic oxytocin secretion. However, α‐MSH inhibition of oxytocin neuron firing is attenuated in mid‐pregnancy and somato‐dendritic oxytocin becomes auto‐excitatory in late‐pregnancy and lactation. Therefore, we hypothesized that attenuated α‐MSH inhibition of oxytocin neuron firing marks the beginning of a transition from inhibition to excitation to facilitate peripheral oxytocin secretion for parturition and lactation. Intra‐SON microdialysis administration of α‐MSH inhibited oxytocin neuron firing rate by 33 ± 9% in non‐pregnant rats but increased oxytocin neuron firing rate by 37 ± 12% in late‐pregnant rats and by 28 ± 10% in lactating rats. α‐MSH‐induced somato‐dendritic oxytocin secretion measured ex vivo with oxytocin receptor‐expressing "sniffer" cells, was of similar amplitude in PVN slices from non‐pregnant and lactating rats but longer‐lasting in slices from lactating rats. Hence, α‐MSH inhibition of oxytocin neuron activity switches to excitation over pregnancy while somato‐dendritic oxytocin secretion is maintained, which might enhance oxytocin neuron excitability to facilitate the increased peripheral secretion that is required for normal parturition and milk ejection. Abstract : Alpha‐MSH activation of somato‐dendritic oxytocin secretion is maintained in pregnancy and lactation but the released oxytocin switches from auto‐inhibition to auto‐excitation to support birth and lactation.