TY - JOUR
T1 - Peptides from frog skin with potential for development into agents for Type 2 diabetes therapy
AU - Conlon, J. Michael
AU - Mechkarska, Milena
AU - Abdel-Wahab, Yasser H.
AU - Flatt, Peter R.
N1 - Funding Information:
Funding for much of the experimental work described in this review was provided by a project grant from Diabetes UK and by the Ulster University Research Strategy Funding program.
Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2018/2
Y1 - 2018/2
N2 - Several frog skin peptides, first identified as result of their antimicrobial or immunomodulatory activities, have subsequently been shown to stimulate insulin release both in vitro and in vivo and so show potential for development into incretin-based drugs for treatment of patients with Type 2 diabetes mellitus. However, their therapeutic potential as anti-diabetic agents is not confined to this activity as certain frog skin-derived peptides, such as magainin-AM2 and CPF-SE1 and analogs of hymenochirin-1B, tigerinin-1R, and esculentin-2CHa, have been shown to increase insulin sensitivity, promote β-cell proliferation, suppress pancreatic and circulating glucagon concentrations, improve the lipid profile, and selectively alter expression of genes involved in insulin secretion and action in mice with diet-induced obesity, insulin resistance and impaired glucose tolerance. This review assesses the therapeutic possibilities of peptides from frogs belonging to the Pipidae, Dicroglossidae, and Ranidae families, focusing upon work that has been carried out since 2014.
AB - Several frog skin peptides, first identified as result of their antimicrobial or immunomodulatory activities, have subsequently been shown to stimulate insulin release both in vitro and in vivo and so show potential for development into incretin-based drugs for treatment of patients with Type 2 diabetes mellitus. However, their therapeutic potential as anti-diabetic agents is not confined to this activity as certain frog skin-derived peptides, such as magainin-AM2 and CPF-SE1 and analogs of hymenochirin-1B, tigerinin-1R, and esculentin-2CHa, have been shown to increase insulin sensitivity, promote β-cell proliferation, suppress pancreatic and circulating glucagon concentrations, improve the lipid profile, and selectively alter expression of genes involved in insulin secretion and action in mice with diet-induced obesity, insulin resistance and impaired glucose tolerance. This review assesses the therapeutic possibilities of peptides from frogs belonging to the Pipidae, Dicroglossidae, and Ranidae families, focusing upon work that has been carried out since 2014.
KW - CPF
KW - Esculentin-2
KW - Frog skin
KW - Host-defense peptide
KW - Hymenochirin
KW - Magainin
KW - Tigerinin
KW - Type 2 diabetes
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U2 - 10.1016/j.peptides.2017.09.001
DO - 10.1016/j.peptides.2017.09.001
M3 - Article
C2 - 28887047
AN - SCOPUS:85041478794
SN - 0196-9781
VL - 100
SP - 275
EP - 281
JO - Peptides
JF - Peptides
ER -