Jw. Kolaczynski et al., A NEW TECHNIQUE FOR BIOPSY OF HUMAN ABDOMINAL FAT UNDER LOCAL-ANESTHESIA WITH LIDOCAINE, International journal of obesity, 18(3), 1994, pp. 161-166
The objectives of this study were to develop a new technique to safely
, reliably, and in a cosmetically acceptable way, obtain more than 5.0
g of abdominal subcutaneous fat in out-patients, and to investigate w
hether inhibitory effects of a local anaesthetic on adipose tissue fun
ction in vitro are sufficient argument against the use of infiltrative
local anaesthesia during fat biopsy to obtain samples for metabolic s
tudies. Measurements were obtained to compare glucose transport and li
polysis response to insulin in adipocytes isolated from subcutaneous a
bdominal fat obtained: (i) during elective surgery in eight women and
four men (BMI 25.8 +/- 3.1 kg/m(2)); and (ii) from five male and three
female out-patients (BMI 25.8 +/- 3.1 kg/m(2)) by the described novel
technique performed under local anaesthesia with Lidocaine. The effec
ts of acute and 11-day exposure to Lidocaine in vitro on adipocyte lip
olysis and glucose transport response to insulin, and the growth poten
tial were determined. In vivo exposure of the tissue samples to local
anaesthetic by the novel technique had no apparent effect on isolated
adipocyte responses to insulin by stimulation of glucose transport or
by inhibitor- or adrenaline-stimulated lipolysis; the results were not
different to those for adipocytes isolated from fat obtained during e
lective abdominal surgeries. Lidocaine added in vitro potently inhibit
ed glucose transport and lipolysis in adipocytes, and cell attachment
and growth in primary 'ceiling' culture; this effect persisted only as
long as Lidocaine was present. After washing, adipocytes fully regain
ed their function and growth regardless of the exposure period, as sho
rt as 30 min or as long as 11 days. Therefore, the proposed novel tech
nique allows rapid sampling of significant amounts of abdominal fat in
outpatients. Lidocaine has an inhibitory effect on adipocyte function
; however, this effect appears to be fully reversible.