Regulation and neurochemical identity of melanin-concentrating hormone neurones in the preoptic area of lactating mice.
Pryscila D S TeixeiraFrederick WasinskiLeandro B LimaRenata FrazãoJackson Cioni BittencourtJose DonatoPublished in: Journal of neuroendocrinology (2019)
Neurones expressing the melanin-concentrating hormone (MCH) can be found in the medial preoptic area (mPOA) and ventral aspects of the periventricular preoptic nucleus of rats by mid-to-late lactation and this expression disappears after weaning. The transitory expression of MCH in the preoptic area suggests a role for these neurones in the control of the end of lactation. However, the neurochemical identity of mPOA MCH neurones and the regulatory factors that control the transient MCH expression remain largely unknown, especially in the mouse. In the present study, we showed that mice also present the transitory expression of MCH in the mPOA at late lactation. mPOA MCH cells did not colocalise significantly with markers of GABAergic (VGAT), glutamatergic (VGLUT2 and VGLUT3) or dopaminergic (tyrosine hydroxylase) neurones. mPOA MCH cells also did not express Kiss1 or oxytocin. By contrast, approximately 70% and 90% of mPOA MCH neurones colocalised with oestrogen receptor α and prolactin-induced phosphorylated signal transducer and activator of transcription 5 (STAT5), respectively. Finally, we demonstrated that the number of MCH neurones in the mPOA is significantly higher in females during the first lactation, compared to mice on the second lactation or pregnant mice during the first lactation or brain-specific STAT5 knockout mice during the first lactation. In summary, our findings indicate that MCH neurones in the mPOA of lactating mice are sensitive to oestrogens and prolactin. Thus, mPOA MCH expression is possibly influenced by hormonal variations. Furthermore, the STAT5 signalling pathway is likely involved in the regulation of MCH expression in the mPOA of lactating mice.
Keyphrases
- dairy cows
- poor prognosis
- human milk
- high fat diet induced
- binding protein
- cell proliferation
- pregnant women
- induced apoptosis
- type diabetes
- magnetic resonance imaging
- insulin resistance
- heat stress
- cell cycle arrest
- cell death
- immune response
- adipose tissue
- spinal cord injury
- multiple sclerosis
- white matter
- metabolic syndrome
- endoplasmic reticulum stress
- functional connectivity
- extracorporeal membrane oxygenation