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Fragment analogs as better mimics of obestatin.
- Source :
-
Regulatory peptides [Regul Pept] 2009 Nov 27; Vol. 158 (1-3), pp. 143-8. Date of Electronic Publication: 2009 Aug 25. - Publication Year :
- 2009
-
Abstract
- Obestatin is a twenty three amino acid peptide produced in the stomach by post translational modification of the preproghrelin gene. Since its discovery in 2005, many studies have shown that obestatin reduces feed intake and gain in body weight in rodents. Studies from our laboratory have shown the N-terminal thirteen residues mimic obestatin the best and residues 6-18 reduce epididymal fat significantly in adult male mice. In this study we have tried to increase the efficacy of these fragments. As an initial step, we have substituted G(8) with alpha-aminoisobutyricacid(Aib,U) and F(5) with cyclohexylalanine(Cha) in the N-terminal peptide to obtain two modified peptides and modified the middle fragment (residues 6-18) by substituting both the glycine residues at position 3 and 8 with alpha-aminoisobutyricacid(U). The rationale being, unusual amino acids could protect the peptides from immediate degradation and Aib would also induce secondary structure in these unstructured peptides. The N-terminal fragment with the G(8)U substitution fared the best. It reduced food intake, gain in body weight, levels of cholesterol and triglycerides in the blood, epididymal and perirenal fat in adult male mice similar to that of obestatin. The middle fragment with G(3,8)U double substitution was the second best.
- Subjects :
- Animals
Body Weight drug effects
Chromatography, High Pressure Liquid
Drinking Behavior drug effects
Feeding Behavior drug effects
Ghrelin chemistry
Lipid Metabolism
Mice
Molecular Mimicry
Pancreatin pharmacology
Ghrelin pharmacology
Peptide Fragments pharmacology
Peptide Hormones pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-1686
- Volume :
- 158
- Issue :
- 1-3
- Database :
- MEDLINE
- Journal :
- Regulatory peptides
- Publication Type :
- Academic Journal
- Accession number :
- 19712707
- Full Text :
- https://doi.org/10.1016/j.regpep.2009.08.008