Study of a Newly Synthesized Substance with a Potential to Stimulate ß3-Adrenergic Receptors
KRČMÁŘ J., KOTOLOVÁ H., VESELÁ L., CSÖLLEI J.1, GONĚC T.1, KARPÍŠEK M., BARTOŠOVÁ L., NEČAS J.
Veterinární a farmaceutická univerzita Brno, Farmaceutická fakulta, Ústav humánní farmakologie a toxikologie 1Veterinární a farmaceutická univerzita Brno, Farmaceutická fakulta, Ústav chemických léčiv |
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Summary:
ß3-adrenoreceptor agonists can stimulate lipolysis in the white adipose tissue and thermogenesis in the brown
adipose tissue. These activities could be useful in the treatment of obesity and the associated metabolic
syndrome. The effects of six-week oral administration of the newly synthesized substance B496 (methyl-4-[2-
-[2-hydroxy-3-(4-ethylcarbamoyl)phenoxyprophyl]amino]etyl)-phenoxyacetate hydrochloride) on serum
glucose, triglycerides, total cholesterol, and leptin levels were studied in male Wistar rats fed with a high-fat diet.
The animals were divided into a group treated with B496 (5 mg dissolved in 1 litre of water) and a control group.
The results indicated a significant reduction in serum glucose levels (-26 %, p<0,01), triacylglyceride levels
(-21 %, p<0,05) and leptin levels (-43 %, p<0,01). Further the effect of a single intraperitoneal dose (1 mg/kg)
of B496 and BRL-37344 on serum leptin levels in the C57Bl/6J mouse was investigated. Administration of
BRL-37344 resulted in a significant decrease in serum leptin levels (-55 %, p<0,001). This reduction was not
demonstrated by newly synthesized substance B496.
Key words:
ß3-adrenoreceptor agonist – aryloxypropanolamines – leptin – BRL-37344
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