J. Robidoux et al., SITE-SPECIFIC EFFECTS OF SYMPATHECTOMY ON THE ADRENERGIC CONTROL OF LIPOLYSIS IN HAMSTER FAT-CELLS, Canadian journal of physiology and pharmacology, 73(4), 1995, pp. 450-458
Regional variations in the response of adipose tissue to lipolytic sti
muli have been suggested to be involved in the development of visceral
adiposity-related morbidity and mortality. Moreover, studies in human
s and in laboratory rodents such as hamsters have shown that the respo
nse of adipocytes to catecholamines depends on their anatomical origin
. The aim of the present study was to investigate the relative involve
ment of the adrenal medulla and of the sympathetic nervous system on r
egional differences in the adrenergic control of lipolysis in isolated
adipocytes from inguinal and epididymal adipose tissues. For this pur
pose, we carried out adrenal demedullation or chemical sympathectomy i
n hamsters. The results confirmed that epididymal adipocytes were sign
ificantly more responsive to beta-adrenergic stimulation than inguinal
adipocytes (p less than or equal to 0.05). This site specificity coul
d originate at a step distal to receptors since tissues exhibited a si
milar number of binding sites for [I-125]cyanopindolol. No significant
regional differences were observed in the alpha(2)-adrenergic antilip
olytic response, with the exception of the clonidine EC(50). A 14-day
sympathectomy significantly increased the beta-adrenergic lipolytic re
sponse only in inguinal adipocytes (p less than or equal to 0.05), and
increased the alpha(2)-adrenergic response only in epididymal adipocy
tes (p less than or equal to 0.05). On the other hand, adrenal demedul
lation had no effect on both adrenergic pathways. These results sugges
t that the sympathetic tone of adipose tissues could be involved in th
e alpha(2)- and beta-adrenergic site-specific response in hamster fat
cells. The 33% increase of the beta-response in inguinal fat cells and
the 38% increase of the alpha(2)-response in epididymal fat cells als
o suggest that the sympathetic pathway favors the lipolytic activation
of the epididymal adipose tissue.