Streptozotocin induces lipolysis in rat adipocytes in vitro
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
12234117
Knihovny.cz E-resources
- MeSH
- Epinephrine pharmacology MeSH
- Hypoglycemic Agents pharmacology MeSH
- Enzyme Inhibitors pharmacology MeSH
- Insulin pharmacology MeSH
- Isoquinolines pharmacology MeSH
- Rats MeSH
- Lipolysis drug effects MeSH
- Rats, Wistar MeSH
- Antibiotics, Antineoplastic pharmacology MeSH
- Streptozocin pharmacology MeSH
- Sulfonamides * MeSH
- Sympathomimetics pharmacology MeSH
- In Vitro Techniques MeSH
- Adipocytes cytology drug effects metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Epinephrine MeSH
- Hypoglycemic Agents MeSH
- Enzyme Inhibitors MeSH
- Insulin MeSH
- Isoquinolines MeSH
- N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide MeSH Browser
- Antibiotics, Antineoplastic MeSH
- Streptozocin MeSH
- Sulfonamides * MeSH
- Sympathomimetics MeSH
Streptozotocin (STZ) is used to induce experimental diabetes in animals and is also applied for the treatment of patients with insulinoma. The aim of the present work was to investigate the direct effect of STZ on lipolysis in isolated rat adipocytes. After the isolation, the cells were incubated in a Krebs-Ringer buffer of pH 7.4, at the temperature 37 degrees C for 90 min with different concentrations of STZ: 0.5, 1 or 2 mmol/l. STZ caused a significant rise in basal values (99%, 199%, and 377%, respectively) and epinephrine-stimulated (1 micromol/l) lipolysis (15%, 24% and 46%, respectively). Augmentation of basal lipolysis by STZ was neither restricted by insulin (1 nmol/l) nor by H-89 (an inhibitor of protein kinase A, 50 micromol/l). These results indicate the stimulatory influence of STZ on the action of hormone-sensitive lipase in isolated cells of white adipose tissue. The obtained outcomes suggest that in studies employing STZ, it is necessary to consider its direct effect upon lipolysis in adipocytes.