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Kisspeptin a potential therapeutic target in treatment of both metabolic and reproductive dysfunction

  • Joanna Helena Sliwowska
  • , Nicola Elizabeth Woods
  • , Abdullah Rzgallah Alzahrani
  • , Elpiniki Paspali
  • , Rothwelle Joseph Tate
  • , Valerie Anne Ferro

Research output: Contribution to journal › Article › peer-review

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Abstract

Kisspeptins (KPs) are proteins that were first recognized to have antimetastatic action. Later, the critical role of this peptide in the regulation of reproduction was proved. In recent years, evidence has been accumulated supporting a role for KPs in regulating metabolic processes in a sexual dimorphic manner. It has been proposed that KPs regulate metabolism both indirectly via gonadal hormones and/or directly via the kisspeptin receptor in the brain, brown adipose tissue, and pancreas. The aim of the review is to provide both experimental and clinical evidence indicating that KPs are peptides linking metabolism and reproduction. We propose that KPs could be used as a potential target to treat both metabolic and reproductive abnormalities. Thus, we focus on the consequences of disruptions in KPs and their receptors in metabolic conditions such as diabetes, undernutrition, obesity, and reproductive disorders (hypogonadotropic hypogonadism and polycystic ovary syndrome). Data from both animal models and human subjects indicate that alterations in KPs in the case of metabolic imbalance lead also to disruptions in reproductive functions. Changes both in the hypothalamic and peripheral KP systems in animal models of the aforementioned disorders are discussed. Finally, an overview of current clinical studies involving KP in fertility and metabolism show fewer studies on metabolism (15%) and only one to date on both. Presented data indicate a dynamic and emerging field of KP studies as possible therapeutic targets in treatments of both reproductive and metabolic dysfunctions.
Original languageEnglish
Article numbere13541
Number of pages15
JournalJournal of Diabetes
Volume16
Issue number4
Early online date10 Apr 2024
DOIs
Publication statusPublished - 10 Apr 2024

Funding

Nicola Woods was sponsored through a Biotechnology and Biological Sciences Research Council (BBSRC) Case studentship: grant number BB/F017642/1. Abdullah Alzahrani was funded by the Royal Embassy of Saudi Arabi-Saudi Cultural Bureau in London. Elpiniki Paspali is sponsored through a University of Strathclyde studentship. Joanna Sliwowska is supported by the National Science Centre in Krakow, Poland (OPUS grant 2015/17/B/NZ4/02021) and the statutory funding (506-511-09-00) from the Faculty of Veterinary Medicine and Animal Science, Poznan University of Life Sciences, Poland to Joanna Sliwowska. Nicola Woods was sponsored through a Biotechnology and Biological Sciences Research Council (BBSRC) Case studentship: grant number BB/F017642/1. Abdullah Alzahrani was funded by the Royal Embassy of Saudi Arabi\u2010Saudi Cultural Bureau in London. Elpiniki Paspali is sponsored through a University of Strathclyde studentship. Joanna Sliwowska is supported by the National Science Centre in Krakow, Poland (OPUS grant 2015/17/B/NZ4/02021) and the statutory funding (506\u2010511\u201009\u201000) from the Faculty of Veterinary Medicine and Animal Science, Poznan University of Life Sciences, Poland to Joanna Sliwowska.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • diabetes mellitus
  • kisspeptin
  • KISS1/Kiss1
  • KISS1R/Kiss1r
  • obesity
  • reproduction

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