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The Case Study of Nesfatin-1 in the Pancreas of Tursiops truncatus.

Authors :
Gatta, Claudia
De Felice, Elena
D'Angelo, Livia
Maruccio, Lucianna
Leggieri, Adele
Lucini, Carla
Palladino, Antonio
Paolucci, Marina
Scocco, Paola
Varricchio, Ettore
de Girolamo, Paolo
Source :
Frontiers in Physiology; 12/19/2018, pN.PAG-N.PAG, 6p
Publication Year :
2018

Abstract

Nesfatin-1 (Nesf-1) is an anorexigenic peptide involved in the regulation of homeostatic feeding. Nesf-1 is expressed in the central nervous system and other organs, including pancreas, where it promotes the release of insulin from β-cells. This raises the possibility that Nesf-1 dysfunction could be involved in metabolic disorders, particularly in type 2 diabetes mellitus (T2D). Recently, it has been discovered that dolphins can be a natural animal model that fully replicates human T2D, due to its prolonged glucose tolerance curve and maintenance of a state of hyperglycemia similar to human T2D during fasting. This correspondence suggests that dolphins may be a suitable model for investigating physiological and pathological metabolic disorders. Here, we have characterized Nesf-1 distribution in the pancreas of the common bottlenose dolphin (Tursiops truncatus) and measured plasmatic levels of Nesf-1 and glucose during fasting and post-prandial states. The Mediterranean Marine Mammal Tissue Bank (MMMTB) of the University of Padova provided us with pancreas samples, derived from four animals, and plasma samples, collected before and after the main meal. Interestingly, our results showed that Nesf-1-immunoreactive cells were distributed in Langerhans islets, co-localized with glucagon in α-cells. Similar to humans, dolphin plasma Nesf-1 concentration doesn't show a statistically significant difference when comparing fasting and post-prandial states. On the other hand, blood glucose levels were significantly higher before than after the main meal. Our data provide a comparative analysis for further studies on the involvement of Nesf-1 in mammalian metabolic disorders. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1664042X
Database :
Complementary Index
Journal :
Frontiers in Physiology
Publication Type :
Academic Journal
Accession number :
134405183
Full Text :
https://doi.org/10.3389/fphys.2018.01845