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Galanin family peptides: Molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord

Galanin is a neurohormone as well as a neurotransmitter and plays versatile physiological roles for the neuroendocrine axis, such as regulating food intake, insulin level and somatostatin release. It is expressed in the central nervous system, including hypothalamus, pituitary, and the spinal cord,...

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Autores principales: Zhu, Sipin, Hu, Xiaoyong, Bennett, Samuel, Charlesworth, Oscar, Qin, Shengnan, Mai, Yuliang, Dou, Haicheng, Xu, Jiake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764007/
https://www.ncbi.nlm.nih.gov/pubmed/36561569
http://dx.doi.org/10.3389/fendo.2022.1019943
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author Zhu, Sipin
Hu, Xiaoyong
Bennett, Samuel
Charlesworth, Oscar
Qin, Shengnan
Mai, Yuliang
Dou, Haicheng
Xu, Jiake
author_facet Zhu, Sipin
Hu, Xiaoyong
Bennett, Samuel
Charlesworth, Oscar
Qin, Shengnan
Mai, Yuliang
Dou, Haicheng
Xu, Jiake
author_sort Zhu, Sipin
collection PubMed
description Galanin is a neurohormone as well as a neurotransmitter and plays versatile physiological roles for the neuroendocrine axis, such as regulating food intake, insulin level and somatostatin release. It is expressed in the central nervous system, including hypothalamus, pituitary, and the spinal cord, and colocalises with other neuronal peptides within neurons. Structural analyses reveal that the human galanin precursor is 104 amino acid (aa) residues in length, consisting of a mature galanin peptide (aa 33-62), and galanin message-associated peptide (GMAP; aa 63-104) at the C-terminus. GMAP appears to exhibit distinctive biological effects on anti-fungal activity and the spinal flexor reflex. Galanin-like peptide (GALP) has a similar structure to galanin and acts as a hypothalamic neuropeptide to mediate metabolism and reproduction, food intake, and body weight. Alarin, a differentially spliced variant of GALP, is specifically involved in vasoactive effect in the skin and ganglionic differentiation in neuroblastic tumors. Dysregulation of galanin, GALP and alarin has been implicated in various neuroendocrine conditions such as nociception, Alzheimer’s disease, seizures, eating disorders, alcoholism, diabetes, and spinal cord conditions. Further delineation of the common and distinctive effects and mechanisms of various types of galanin family proteins could facilitate the design of therapeutic approaches for neuroendocrine diseases and spinal cord injury.
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spelling pubmed-97640072022-12-21 Galanin family peptides: Molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord Zhu, Sipin Hu, Xiaoyong Bennett, Samuel Charlesworth, Oscar Qin, Shengnan Mai, Yuliang Dou, Haicheng Xu, Jiake Front Endocrinol (Lausanne) Endocrinology Galanin is a neurohormone as well as a neurotransmitter and plays versatile physiological roles for the neuroendocrine axis, such as regulating food intake, insulin level and somatostatin release. It is expressed in the central nervous system, including hypothalamus, pituitary, and the spinal cord, and colocalises with other neuronal peptides within neurons. Structural analyses reveal that the human galanin precursor is 104 amino acid (aa) residues in length, consisting of a mature galanin peptide (aa 33-62), and galanin message-associated peptide (GMAP; aa 63-104) at the C-terminus. GMAP appears to exhibit distinctive biological effects on anti-fungal activity and the spinal flexor reflex. Galanin-like peptide (GALP) has a similar structure to galanin and acts as a hypothalamic neuropeptide to mediate metabolism and reproduction, food intake, and body weight. Alarin, a differentially spliced variant of GALP, is specifically involved in vasoactive effect in the skin and ganglionic differentiation in neuroblastic tumors. Dysregulation of galanin, GALP and alarin has been implicated in various neuroendocrine conditions such as nociception, Alzheimer’s disease, seizures, eating disorders, alcoholism, diabetes, and spinal cord conditions. Further delineation of the common and distinctive effects and mechanisms of various types of galanin family proteins could facilitate the design of therapeutic approaches for neuroendocrine diseases and spinal cord injury. Frontiers Media S.A. 2022-12-06 /pmc/articles/PMC9764007/ /pubmed/36561569 http://dx.doi.org/10.3389/fendo.2022.1019943 Text en Copyright © 2022 Zhu, Hu, Bennett, Charlesworth, Qin, Mai, Dou and Xu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Zhu, Sipin
Hu, Xiaoyong
Bennett, Samuel
Charlesworth, Oscar
Qin, Shengnan
Mai, Yuliang
Dou, Haicheng
Xu, Jiake
Galanin family peptides: Molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord
title Galanin family peptides: Molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord
title_full Galanin family peptides: Molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord
title_fullStr Galanin family peptides: Molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord
title_full_unstemmed Galanin family peptides: Molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord
title_short Galanin family peptides: Molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord
title_sort galanin family peptides: molecular structure, expression and roles in the neuroendocrine axis and in the spinal cord
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764007/
https://www.ncbi.nlm.nih.gov/pubmed/36561569
http://dx.doi.org/10.3389/fendo.2022.1019943
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