MECHANISMS IN ENDOCRINOLOGY: The physiology of neuronostatin
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MECHANISMS IN ENDOCRINOLOGY : The physiology of neuronostatin. / Andersen, Mads R.; Suppli, Malte P.; Bagger, Jonatan I.; Christensen, Mikkel B.; Yosten, Gina L.C.; Knop, Filip K.; Lund, Asger.
In: European Journal of Endocrinology, Vol. 185, No. 4, 2021, p. R93-R101.Research output: Contribution to journal › Review › Research › peer-review
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TY - JOUR
T1 - MECHANISMS IN ENDOCRINOLOGY
T2 - The physiology of neuronostatin
AU - Andersen, Mads R.
AU - Suppli, Malte P.
AU - Bagger, Jonatan I.
AU - Christensen, Mikkel B.
AU - Yosten, Gina L.C.
AU - Knop, Filip K.
AU - Lund, Asger
PY - 2021
Y1 - 2021
N2 - In 2008, the first evidence of a new hormone called neuronostatin was published. The hormone was discovered using a bioinformatic method and found to originate from the same preprohormone as somatostatin. This small peptide hormone of 13 amino acids and a C-terminal amidation was soon found to exert pleiotropic physiological effects. In animal studies, neuronostatin has been shown to reduce food intake and delay gastric emptying and gastrointestinal transit. Furthermore, neuronostatin has been shown to affect glucose metabolism by increasing glucagon secretion during situations when glucose concentrations are low. Additionally, neuronostatin has been shown to affect neural tissue and cardiomyocytes by suppressing cardiac contractility. The effects of neuronostatin have not yet been delineated in humans, but if the effects found in animal studies translate to humans it could position neuronostatin as a promising target in the treatment of obesity, hypertension and diabetes. In this review, we describe the discovery of neuronostatin and the current understanding of its physiological role and potential therapeutic applicability.
AB - In 2008, the first evidence of a new hormone called neuronostatin was published. The hormone was discovered using a bioinformatic method and found to originate from the same preprohormone as somatostatin. This small peptide hormone of 13 amino acids and a C-terminal amidation was soon found to exert pleiotropic physiological effects. In animal studies, neuronostatin has been shown to reduce food intake and delay gastric emptying and gastrointestinal transit. Furthermore, neuronostatin has been shown to affect glucose metabolism by increasing glucagon secretion during situations when glucose concentrations are low. Additionally, neuronostatin has been shown to affect neural tissue and cardiomyocytes by suppressing cardiac contractility. The effects of neuronostatin have not yet been delineated in humans, but if the effects found in animal studies translate to humans it could position neuronostatin as a promising target in the treatment of obesity, hypertension and diabetes. In this review, we describe the discovery of neuronostatin and the current understanding of its physiological role and potential therapeutic applicability.
U2 - 10.1530/EJE-21-0347
DO - 10.1530/EJE-21-0347
M3 - Review
C2 - 34370694
AN - SCOPUS:85115897464
VL - 185
SP - R93-R101
JO - European Journal of Endocrinology
JF - European Journal of Endocrinology
SN - 0804-4643
IS - 4
ER -
ID: 281648925