Title of article :
Hypertension in cafeteria-fed rats: alterations in renal α2-adrenoceptor subtypes
Author/Authors :
Gwenn Coatmellec-Taglioni، نويسنده , , Jean-Pierre Dausse، نويسنده , , Catherine Ribière، نويسنده , , Yves Giudicelli، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Pages :
6
From page :
529
To page :
534
Abstract :
Obesity is a major cause of human essential hypertension and there are clear evidences that abnormal kidney functions play a key role in obesity hypertension. Feeding rats a cafeteria diet has been extensively used as an experimental model to study obesity and energy balance expenditure. The present study investigated whether rats fed a cafeteria diet develop hypertension with alterations in renal α2-adrenoceptor subtype distribution. Weight gain induced by feeding rats a cafeteria diet during 8 weeks was associated with a marked increase in blood pressure. Insulin levels were higher in these hypertensive rats, leading to a decreased plasma glucose/insulin ratio. Based on radioligand-binding studies using [3H]-RX821002 and selective competitors, a raise in α2-adrenoceptor density that was solely due to an increased α2B-adrenoceptor subtype density was detected in the kidney of the cafeteria-fed rat. Furthermore, reverse transcription-polymerase chain reaction (RT-PCR) experiments showed an overexpression of the gene encoding the α2B-adrenoceptor subtype in these rats. On the other hand, despite a similar mRNA level, the α2A-adrenoceptor subtype was no more detectable by radioligand-binding studies in the kidney of the cafeteria-fed rat. In conclusion, cafeteria-fed rats are hypertensive, with renal alterations in α2-adrenoceptor distribution. These alterations, which are not related to genetic factors, may play a key role in the onset of hypertension.
Keywords :
hypertension , cafeteria diet , a2-adrenoceptor subtypes , Obesity. , Blood pressure
Journal title :
American Journal of Hypertension
Serial Year :
2000
Journal title :
American Journal of Hypertension
Record number :
647572
Link To Document :
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