z-logo
open-access-imgOpen Access
Neuroendocrine hormone amylin in diabetes
Author(s) -
Xiaoxi Zhang,
Yanhong Pan,
Yan-Mei Huang,
Hai-Lu Zhao
Publication year - 2016
Publication title -
world journal of diabetes
Language(s) - Uncategorized
Resource type - Journals
ISSN - 1948-9358
DOI - 10.4239/wjd.v7.i9.189
Subject(s) - amylin , islet , endocrinology , medicine , amyloid (mycology) , diabetes mellitus , pancreatic islets , hormone , type 2 diabetes , glucose homeostasis , angiotensin ii , receptor , insulin resistance , pathology
The neuroendocrine hormone amylin, also known as islet amyloid polypeptide, is co-localized, co-packaged and co-secreted with insulin from adult pancreatic islet β cells to maintain glucose homeostasis. Specifically, amylin reduces secretion of nutrient-stimulated glucagon, regulates blood pressure with an effect on renin-angiotensin system, and delays gastric emptying. The physiological actions of human amylin attribute to the conformational α-helix monomers whereas the misfolding instable oligomers may be detrimental to the islet β cells and further transform to β-sheet fibrils as amyloid deposits. No direct evidence proves that the amylin fibrils in amyloid deposits cause diabetes. Here we also have performed a systematic review of human amylin gene changes and reported the S20G mutation is minor in the development of diabetes. In addition to the metabolic effects, human amylin may modulate autoimmunity and innate inflammation through regulatory T cells to impact on both human type 1 and type 2 diabetes.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here