| Autor: |
Maldonado, Marcos Rodrigues, Bracht, Lívia, de Sá‐Nakanishi, Anacharis Babeto, Corrêa, Rúbia Carvalho Gomes, Comar, Jurandir Fernando, Peralta, Rosane Marina, Bracht, Adelar |
| Zdroj: |
Cell Biochemistry & Function; Jan2018, Vol. 36 Issue 1, p4-12, 9p |
| Abstrakt: |
p‐Synephrine is one of the main active components of the fruit of Citrus aurantium (bitter orange). Extracts of the bitter orange and other preparations containing p‐synephrine have been used worldwide to promote weight loss and for sports performance. The purpose of the study was to measure the action of p‐synephrine on hepatic enzyme activities linked to carbohydrate and energy metabolism and the levels of adenine mononucleotides. Enzymes and adenine mononucleotides were measured in the isolated perfused rat liver and in vivo after oral administration of the drug (50 and 300 mg/kg) by using standard techniques. p‐Synephrine increased the activity of glycogen phosphorylase in vivo and in the perfused liver. It decreased, however, the activities of pyruvate kinase and pyruvate dehydrogenase also in vivo and in the perfused liver. p‐Synephrine increased the hepatic pools of adenosine diphosphate and adenosine triphosphate. Stimulation of glycogen phosphorylase is consistent with the reported increased glycogenolysis in the perfused liver and increased glycemia in rats. The decrease in the pyruvate dehydrogenase activity indicates that p‐synephrine is potentially capable of inhibiting the transformation of carbohydrates into lipids. The capability of increasing the adenosine triphosphate‐adenosine diphosphate pool indicates a beneficial effect of p‐synephrine on the cellular energetics. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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