Skin blood flowmotion response to insulin iontophoresis in normal subjects

In order to explore the mechanisms directly involved in the insulin vasodilatory activity, we studied skin blood flowmotion by means of spectral analysis of the skin forearm laser Doppler (LD) signal registered before and after iontophoresis of insulin in saline (I.S.) (0.1 ml Humulin R 100 IU/ml di...

Full description

Saved in:
Bibliographic Details
Published in:Microvascular research Vol. 70; no. 1; pp. 17 - 22
Main Authors: Rossi, M., Maurizio, S., Carpi, A.
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01.07.2005
Subjects:
Adult
Female
Humans
Hypoglycemic Agents - pharmacology
Insulin
Insulin - pharmacology
Iontophoresis
Laser Doppler
Laser-Doppler Flowmetry
Male
Microcirculation
Microcirculation - drug effects
Microvascular smooth muscle cells
Myogenic activity
Skin - blood supply
Skin flowmotion
Iontophoresis
Microcirculation
Laser Doppler
Myogenic activity
Skin flowmotion
Insulin
Microvascular smooth muscle cells
ISSN:0026-2862, 1095-9319
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:In order to explore the mechanisms directly involved in the insulin vasodilatory activity, we studied skin blood flowmotion by means of spectral analysis of the skin forearm laser Doppler (LD) signal registered before and after iontophoresis of insulin in saline (I.S.) (0.1 ml Humulin R 100 IU/ml diluted 1/10 in 0.9% saline) or pure saline (P.S.) (0.1 ml of 0.9% saline) in twenty normal subjects. Skin LD blood perfusion was also measured in conventional perfusion unit (PU; 1 PU = 10 mV). Using a Fast Fourier transform algorithm, power density (PD) of the total flowmotion spectrum, from 0.009 to 1.6 Hz, was measured in PU/Hz. Power density of five skin flowmotion frequency intervals (F.I.) within 0.009–0.02 Hz, 0.02–0.06 Hz, 0.06–0.2 Hz, 0.2–0.6 Hz and 0.6–1.6 Hz (referred to endothelial, sympathetic, myogenic, respiratory and heart activity, respectively) was also measured in PU/Hz. The mean skin LD perfusion increment (expressed as percent change from baseline) was significantly higher after I.S. than after P.S. ( P < 0.001, ANOVA for repeated measures). Skin flowmotion total spectrum mean PD value significantly increased following iontophoresis of both P.S. (from 1.06 ± 0.62 to 1.86 ± 0.94 PU/Hz, P < 0.005) and I.S. (from 1.07 ± 0.92 to 2.39 ± 1.73 PU/Hz P < 0.00005), however, the mean PD increment was significantly higher after I.S. than after P.S. (1.27 ± 0.98 PU/Hz versus 0.69 ± 0.67 PU/Hz, P < 0.05). Only the flowmotion component referred to myogenic activity showed a percent PD increase from baseline significantly higher in response to I.S. than to P.S. iontophoresis (114.5 ± 21.8% versus 58.8 ± 17.9%, respectively, P < 0.05). These findings show that insulin has a vasodilatory activity on skin microvascular district. The higher increase of total blood flowmotion PD and particularly of the component related to the myogenic activity in response to insulin iontophoresis suggests that the cutaneous vasodilatory activity of insulin is, in part, related to an important action of this hormone on skin microvascular smooth muscle.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0026-2862
1095-9319
DOI:10.1016/j.mvr.2005.05.001