Lipidized PrRP Analog Exhibits Strong Anti-Obesity and Antidiabetic Properties in Old WKY Rats with Obesity and Glucose Intolerance
Language English Country Switzerland Media electronic
Document type Journal Article
Grant support
20-00546S
Czech Science Foundation
LX22NP05104
European Union - Next Generation EU
PubMed
36678151
PubMed Central
PMC9864151
DOI
10.3390/nu15020280
PII: nu15020280
Knihovny.cz E-resources
- Keywords
- Wistar Kyoto rats, astrocytosis, diet-induced obesity, glucose intolerance, lipid metabolism, lipidomics, liraglutide, metabolomics, prolactin-releasing peptide,
- MeSH
- Diet, High-Fat adverse effects MeSH
- Prolactin-Releasing Hormone pharmacology MeSH
- Hypoglycemic Agents pharmacology therapeutic use MeSH
- Insulin Resistance * MeSH
- Rats MeSH
- Lipids MeSH
- Liraglutide pharmacology therapeutic use MeSH
- Mice MeSH
- Obesity drug therapy MeSH
- Glucose Intolerance * drug therapy MeSH
- Rats, Inbred WKY MeSH
- Prediabetic State * drug therapy MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Prolactin-Releasing Hormone MeSH
- Hypoglycemic Agents MeSH
- Lipids MeSH
- Liraglutide MeSH
Prolactin-releasing peptide (PrRP) is an anorexigenic neuropeptide that has potential for the treatment of obesity and its complications. Recently, we designed a palmitoylated PrRP31 analog (palm11-PrRP31) that is more stable than the natural peptide and able to act centrally after peripheral administration. This analog acted as an anti-obesity and glucose-lowering agent, attenuating lipogenesis in rats and mice with high-fat (HF) diet-induced obesity. In Wistar Kyoto (WKY) rats fed a HF diet for 52 weeks, we explored glucose intolerance, but also prediabetes, liver steatosis and insulin resistance-related changes, as well as neuroinflammation in the brain. A potential beneficial effect of 6 weeks of treatment with palm11-PrRP31 and liraglutide as comparator was investigated. Liver lipid profiles, as well as urinary and plasma metabolomic profiles, were measured by lipidomics and metabolomics, respectively. Old obese WKY rats showed robust glucose intolerance that was attenuated by palm11-PrRP31, but not by liraglutide treatment. On the contrary, liraglutide had a beneficial effect on insulin resistance parameters. Despite obesity and prediabetes, WKY rats did not develop steatosis owing to HF diet feeding, even though liver lipogenesis was enhanced. Plasma triglycerides and cholesterol were not increased by HFD feeding, which points to unincreased lipid transport from the liver. The liver lipid profile was significantly altered by a HF diet that remained unaffected by palm11-PrRP31 or liraglutide treatment. The HF-diet-fed WKY rats revealed astrogliosis in the brain cortex and hippocampus, which was attenuated by treatment. In conclusion, this study suggested multiple beneficial anti-obesity-related effects of palm11-PrRP31 and liraglutide in both the periphery and brain.
Institute of Microbiology Czech Academy of Sciences 142 20 Prague Czech Republic
Institute of Physiology Czech Academy of Sciences 142 20 Prague Czech Republic
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