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Alternative role for prolactin-releasing peptide in the regulation of food intake

Abstract

Prolactin-releasing peptide (PrRP) is a peptide ligand for the human orphan G-protein-coupled receptor hGR3/GPR10 and causes the secretion of prolactin from anterior pituitary cells1. However, the lack of immunoreactive staining for PrRP in the external layer of the median eminence seems to rule out this peptide as a classical hypophysiotropic hormone2,3,4 and, furthermore, PrRP is less effective than another inducer of prolactin secretion, thyrotropin-releasing hormone, both in vitro and in vivo5,6,7. Here we show a reduction in the expression of PrRP mRNA during lactation and fasting and an acute effect of PrRP on food intake and body weight, supporting the hypothesis of an alternative role for the peptide.

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Figure 1: PrRP affects food intake and core body temperature in free-fed animals.
Figure 2: PrRP reduces fast-induced re-feeding.

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References

  1. Hinuma, S. et al. Nature 393, 272–276 (1998).

    Article  CAS  Google Scholar 

  2. Iijima, N. et al. Neuroreport 10, 1713–1716 (1999).

    Article  CAS  Google Scholar 

  3. Maruyama, M. et al. Endocrinology 140, 2326–2333 (1999).

    Article  CAS  Google Scholar 

  4. Yamakawa, K., Kudo, K., Kanba, S. & Arita, J. Neurosci. Lett. 267, 113–116 (1999).

    Article  CAS  Google Scholar 

  5. Matsumoto, H. et al. Biochem. Biophys. Res. Commun. 259, 321–324 (1999).

    Article  CAS  Google Scholar 

  6. Samson, W. K., Resch, Z. T., Murphy, T. C. & Chang, J. K. Endocrine 9, 289–291 (1998).

    Article  CAS  Google Scholar 

  7. Tokita, R. et al. Neurosci. Lett. 276, 103–106 (1999).

    Article  CAS  Google Scholar 

  8. Roland, B. L. et al. Endocrinology 140, 5736–5745 (1999).

    Article  CAS  Google Scholar 

  9. Ritter, R. C., Covasa, M. & Matson, C. A. Neuropeptides 33, 387–399 (1999).

    Article  CAS  Google Scholar 

  10. Seeley, R. J. et al. J. Neurosci 20, 1616–1621 (2000).

    Article  CAS  Google Scholar 

  11. Elmquist, J. K., Elias, C. F. & Saper, C. B. Neuron 22, 221–232 (1999).

    Article  CAS  Google Scholar 

  12. Bhatnagar, S. & Dallman, M. F. Brain Res. 851, 66–75 (1999).

    Article  CAS  Google Scholar 

  13. Brady, L. S., Smith, M. A., Gold, P. W. & Herkenham, M. Neuroendocrinology 52, 441–447 (1990).

    Article  CAS  Google Scholar 

  14. Kristensen, P. et al. Nature 393, 72–76 (1998).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We acknowledge the support of the Biotechnology and Biosciences Research Council and AstraZeneca plc. We also thank N. Rothwell and A. Turnbull for commenting on the manuscript and A. Hardwick for technical assistance.

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Correspondence to Simon M. Luckman.

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Lawrence, C., Celsi, F., Brennand, J. et al. Alternative role for prolactin-releasing peptide in the regulation of food intake. Nat Neurosci 3, 645–646 (2000). https://doi.org/10.1038/76597

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