Cargando…

Circulating Levels of Human salusin-β,a Potent Hemodynamic and Atherogenesis Regulator

Using bioinformatics analysis, we previously identified salusin-β, an endogenous bioactive peptide with diverse physiological activities. Salusin-β is abundantly expressed in the neuroendocrine system and in systemic endocrine cells/macrophages. Salusin-β acutely regulates hemodynamics and chronical...

Descripción completa

Detalles Bibliográficos
Autores principales: Fujimoto, Kazumi, Hayashi, Akinori, Kamata, Yuji, Ogawa, Akifumi, Watanabe, Takuya, Ichikawa, Raishi, Iso, Yoshitaka, Koba, Shinji, Kobayashi, Youichi, Koyama, Takatoshi, Shichiri, Masayoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789687/
https://www.ncbi.nlm.nih.gov/pubmed/24098553
http://dx.doi.org/10.1371/journal.pone.0076714
_version_ 1782286476022644736
author Fujimoto, Kazumi
Hayashi, Akinori
Kamata, Yuji
Ogawa, Akifumi
Watanabe, Takuya
Ichikawa, Raishi
Iso, Yoshitaka
Koba, Shinji
Kobayashi, Youichi
Koyama, Takatoshi
Shichiri, Masayoshi
author_facet Fujimoto, Kazumi
Hayashi, Akinori
Kamata, Yuji
Ogawa, Akifumi
Watanabe, Takuya
Ichikawa, Raishi
Iso, Yoshitaka
Koba, Shinji
Kobayashi, Youichi
Koyama, Takatoshi
Shichiri, Masayoshi
author_sort Fujimoto, Kazumi
collection PubMed
description Using bioinformatics analysis, we previously identified salusin-β, an endogenous bioactive peptide with diverse physiological activities. Salusin-β is abundantly expressed in the neuroendocrine system and in systemic endocrine cells/macrophages. Salusin-β acutely regulates hemodynamics and chronically induces atherosclerosis, but its unique physicochemical characteristics to tightly adhere to all types of plastic and glassware have prevented elucidation of its precise pathophysiological role. To quantitate plasma total salusin-β concentrations, we produced rabbit and chicken polyclonal antibodies against the C- and N-terminal end sequences, circumvented its sticky nature, and successfully established a sandwich enzyme-linked immunosorbent assay (ELISA). Salusin-β was abundantly present in the plasma of healthy volunteers, ranging from 1.9 to 6.6 nmol/L. Reverse phase-high performance liquid chromatography analysis showed that a single immunoreactive salusin-β peak coincided with synthetic authentic salusin-β. Plasma salusin-β concentrations were unaffected by postural changes and by potent vasopressin release stimuli, such as hypertonic saline infusion or smoking. However, salusin-β concentrations showed significant circadian variation; concentrations were high during the daytime and reached the lowest concentrations in the early morning. Plasma salusin-β levels in subjects with diabetes mellitus, coronary artery disease, and cerebrovascular disease showed distinctly higher levels than healthy controls. Patients with panhypopituitarism combined with complete central diabetes insipidus also showed significantly higher plasma salusin-β levels. Therefore, the ELISA system developed in this study will be useful for evaluating circulating total salusin-β levels and for confirming the presence of authentic salusin-β in human plasma. The obtained results suggest a limited contribution of the neuroendocrine system to peripheral total salusin-β concentrations and a role for plasma total salusin-β concentrations as an indicator of systemic vascular diseases.
format Online
Article
Text
id pubmed-3789687
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37896872013-10-04 Circulating Levels of Human salusin-β,a Potent Hemodynamic and Atherogenesis Regulator Fujimoto, Kazumi Hayashi, Akinori Kamata, Yuji Ogawa, Akifumi Watanabe, Takuya Ichikawa, Raishi Iso, Yoshitaka Koba, Shinji Kobayashi, Youichi Koyama, Takatoshi Shichiri, Masayoshi PLoS One Research Article Using bioinformatics analysis, we previously identified salusin-β, an endogenous bioactive peptide with diverse physiological activities. Salusin-β is abundantly expressed in the neuroendocrine system and in systemic endocrine cells/macrophages. Salusin-β acutely regulates hemodynamics and chronically induces atherosclerosis, but its unique physicochemical characteristics to tightly adhere to all types of plastic and glassware have prevented elucidation of its precise pathophysiological role. To quantitate plasma total salusin-β concentrations, we produced rabbit and chicken polyclonal antibodies against the C- and N-terminal end sequences, circumvented its sticky nature, and successfully established a sandwich enzyme-linked immunosorbent assay (ELISA). Salusin-β was abundantly present in the plasma of healthy volunteers, ranging from 1.9 to 6.6 nmol/L. Reverse phase-high performance liquid chromatography analysis showed that a single immunoreactive salusin-β peak coincided with synthetic authentic salusin-β. Plasma salusin-β concentrations were unaffected by postural changes and by potent vasopressin release stimuli, such as hypertonic saline infusion or smoking. However, salusin-β concentrations showed significant circadian variation; concentrations were high during the daytime and reached the lowest concentrations in the early morning. Plasma salusin-β levels in subjects with diabetes mellitus, coronary artery disease, and cerebrovascular disease showed distinctly higher levels than healthy controls. Patients with panhypopituitarism combined with complete central diabetes insipidus also showed significantly higher plasma salusin-β levels. Therefore, the ELISA system developed in this study will be useful for evaluating circulating total salusin-β levels and for confirming the presence of authentic salusin-β in human plasma. The obtained results suggest a limited contribution of the neuroendocrine system to peripheral total salusin-β concentrations and a role for plasma total salusin-β concentrations as an indicator of systemic vascular diseases. Public Library of Science 2013-10-03 /pmc/articles/PMC3789687/ /pubmed/24098553 http://dx.doi.org/10.1371/journal.pone.0076714 Text en © 2013 Fujimoto et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fujimoto, Kazumi
Hayashi, Akinori
Kamata, Yuji
Ogawa, Akifumi
Watanabe, Takuya
Ichikawa, Raishi
Iso, Yoshitaka
Koba, Shinji
Kobayashi, Youichi
Koyama, Takatoshi
Shichiri, Masayoshi
Circulating Levels of Human salusin-β,a Potent Hemodynamic and Atherogenesis Regulator
title Circulating Levels of Human salusin-β,a Potent Hemodynamic and Atherogenesis Regulator
title_full Circulating Levels of Human salusin-β,a Potent Hemodynamic and Atherogenesis Regulator
title_fullStr Circulating Levels of Human salusin-β,a Potent Hemodynamic and Atherogenesis Regulator
title_full_unstemmed Circulating Levels of Human salusin-β,a Potent Hemodynamic and Atherogenesis Regulator
title_short Circulating Levels of Human salusin-β,a Potent Hemodynamic and Atherogenesis Regulator
title_sort circulating levels of human salusin-β,a potent hemodynamic and atherogenesis regulator
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789687/
https://www.ncbi.nlm.nih.gov/pubmed/24098553
http://dx.doi.org/10.1371/journal.pone.0076714
work_keys_str_mv AT fujimotokazumi circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT hayashiakinori circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT kamatayuji circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT ogawaakifumi circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT watanabetakuya circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT ichikawaraishi circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT isoyoshitaka circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT kobashinji circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT kobayashiyouichi circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT koyamatakatoshi circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator
AT shichirimasayoshi circulatinglevelsofhumansalusinbapotenthemodynamicandatherogenesisregulator