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		<title>Admin at 05:39, 22 August 2008</title>
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		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;AN   &lt;br /&gt;
     1999:39502  DISSABS   Order Number: AAIC701050 (not available for sale by&lt;br /&gt;
     UMI)&lt;br /&gt;
TI   &lt;br /&gt;
     EFFECTS ON ENERGY UTILIZATION AND EXPRESSION OF THE OBESITY GENE AND&lt;br /&gt;
     UNCOUPLING PROTEINS (UCP1 AND UCP2) BY NEW BETA-3 ADRENERGIC AGONIST IN&lt;br /&gt;
     RATS FED A CAFETERIA DIET&lt;br /&gt;
     EFECTOS EN LA UTILIZACION ENERGETICA Y EN LA EXPRESION DEL GEN DE LA&lt;br /&gt;
     OBESIDAD Y PROTEINAS DESACOPLANTES (UCP1 Y UCP3) DE UN NUEVO AGONISTA&lt;br /&gt;
     ADRENERGICO BETA3 EN UN MODELO DE OBESIDAD INDUCIDA CON UNA DIETA DE&lt;br /&gt;
     CAFETERIA&lt;br /&gt;
AU   &lt;br /&gt;
     BERRAONDO LOPEZ, BEATRIZ [DR.]&lt;br /&gt;
CS   &lt;br /&gt;
     UNIVERSIDAD DE NAVARRA (SPAIN) (5864)&lt;br /&gt;
SO   &lt;br /&gt;
     Dissertation Abstracts International, (1998) Vol. 60, No. 2C, p. 362.&lt;br /&gt;
     Order No.: AAIC701050 (not available for sale by UMI). 286 pages. FACULTY&lt;br /&gt;
     OF PHARMACY, UNIVERSITY OF NAVARRA, E-31080 PAMPLONA, SPAIN. &lt;br /&gt;
DT   &lt;br /&gt;
     Dissertation&lt;br /&gt;
FS   &lt;br /&gt;
     DAI&lt;br /&gt;
LA   &lt;br /&gt;
     Spanish&lt;br /&gt;
AB   &lt;br /&gt;
         The $\beta3$-adrenergic agonists demonstrate major lipolytic,&lt;br /&gt;
     thermogenic and hypoglucaemic effects, and are potentially applicable in&lt;br /&gt;
     the treatment of obesity and diabetes. In this paper, we study the&lt;br /&gt;
     effects on energy consumption and the expression of the obesity gene and&lt;br /&gt;
     uncoupling proteins (UCP1 and UCP2) when the new $\beta3$-adrenergic&lt;br /&gt;
     agonist, Trecadrine, was administered for 35 days in a model of obesity&lt;br /&gt;
     induced by a cafeteria diet in female Wistar rats. Trecadrine (1 mg/kg)&lt;br /&gt;
     was given to the obese animals, and was found to reduce significantly&lt;br /&gt;
     their body weight and fat deposits as a result of an increase in lipolysis&lt;br /&gt;
     in the white and brown fat, as Trecadrine increases the activity of&lt;br /&gt;
     hormone-sensitive lipase and the consumption of oxygen in vitro in&lt;br /&gt;
     white fat. At the same time, the administration of Trecadrine (1 mg/kg) to&lt;br /&gt;
     obese rats produced an increase in thermogenesis, mediated by a rise in&lt;br /&gt;
     UCP1 expression in brown fat and UCP2 in the gastrocnemius muscle, the&lt;br /&gt;
     principal modulators of which seem to be the fatty acids which are&lt;br /&gt;
     mobilized when lipolysis is stimulated. However, UCP2 expression in the&lt;br /&gt;
     gastrocnemius was reduced in control rats treated with Trecadrine (1&lt;br /&gt;
     mg/kg), which suggests that the response was different in control animals&lt;br /&gt;
     from that in obese ones. Similarly, the administration of Trecadrine (1&lt;br /&gt;
     mg/kg) to obese animals brought down the plasma leptin levels and the&lt;br /&gt;
     amount of obesity gene which was expressed. In conclusion, Trecadrine&lt;br /&gt;
     could be of great interest for the treatment of obesity.&lt;br /&gt;
CC   &lt;br /&gt;
     0570 HEALTH SCIENCES, NUTRITION; 0307 BIOLOGY, MOLECULAR; 0433 BIOLOGY,&lt;br /&gt;
     ANIMAL PHYSIOLOGY&lt;/div&gt;</summary>
		<author><name>Admin</name></author>	</entry>

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