-
Something wrong with this record ?
Monitoring of Caffeine Consumption Effect on Skin Blood Properties by Diffuse Reflectance Spectroscopy
M. Milanic, R. Hren, J. Stergar, U. Simoncic
Status minimal Language English Country Czech Republic
Document type Journal Article
NLK
Directory of Open Access Journals
from 1991
Free Medical Journals
from 1998
PubMed Central
from 2020
ProQuest Central
from 2005-01-01
Medline Complete (EBSCOhost)
from 2006-01-01
Nursing & Allied Health Database (ProQuest)
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- Caffeine * MeSH
- Skin * blood supply MeSH
- Humans MeSH
- Spectrum Analysis methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Caffeine is the most widely consumed psychoactive substance worldwide, affecting numerous tissues and organs, with notable impacts on the central nervous system, heart, and blood vessels. The effect of caffeine on vascular smooth muscle cells is an initial transient contraction followed by significant vasodilatation. In this study we investigate the use of diffuse reflectance spectroscopy (DRS) for monitoring of vascular changes in human skin induced by caffeine consumption. DRS spectra were recorded on volar sides of the forearms of eight healthy volunteers at time intervals of 0, 30, 60, 120, and 180 min after consumption of caffeine, while one subject served as a negative control. Analytical diffusion approximation solutions for diffuse reflectance from three-layer structures were used to assess skin composition (e.g. dermal blood volume fraction and oxygen saturation) by fitting these solutions to experimental data. The results demonstrate that cutaneous vasodynamics induced by caffeine consumption can be monitored by DRS, while changes in the control subject not consuming caffeine were insignificant.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc24008660
- 003
- CZ-PrNML
- 005
- 20250807160351.0
- 007
- ta
- 008
- 240509s2024 xr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.935138 $2 doi
- 035 __
- $a (PubMed)38466004
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Milanic, M. $u Faculty of Mathematics and Physics, University of Ljubljana, Ljubljana, Republic of Slovenia. matija.milanic@fmf.uni-lj.si
- 245 10
- $a Monitoring of Caffeine Consumption Effect on Skin Blood Properties by Diffuse Reflectance Spectroscopy / $c M. Milanic, R. Hren, J. Stergar, U. Simoncic
- 520 9_
- $a Caffeine is the most widely consumed psychoactive substance worldwide, affecting numerous tissues and organs, with notable impacts on the central nervous system, heart, and blood vessels. The effect of caffeine on vascular smooth muscle cells is an initial transient contraction followed by significant vasodilatation. In this study we investigate the use of diffuse reflectance spectroscopy (DRS) for monitoring of vascular changes in human skin induced by caffeine consumption. DRS spectra were recorded on volar sides of the forearms of eight healthy volunteers at time intervals of 0, 30, 60, 120, and 180 min after consumption of caffeine, while one subject served as a negative control. Analytical diffusion approximation solutions for diffuse reflectance from three-layer structures were used to assess skin composition (e.g. dermal blood volume fraction and oxygen saturation) by fitting these solutions to experimental data. The results demonstrate that cutaneous vasodynamics induced by caffeine consumption can be monitored by DRS, while changes in the control subject not consuming caffeine were insignificant.
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a kofein $7 D002110
- 650 12
- $a kůže $x krevní zásobení $7 D012867
- 650 _2
- $a spektrální analýza $x metody $7 D013057
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Hren, R.
- 700 1_
- $a Stergar, J.
- 700 1_
- $a Simoncic, U.
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 73, č. 1 (2024), s. 47-56
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/38466004 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y - $z 0
- 990 __
- $a 20240509 $b ABA008
- 991 __
- $a 20250807160346 $b ABA008
- 999 __
- $a min $b bmc $g 2283478 $s 1218441
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 73 $c 1 $d 47-56 $e 20240311 $i 1802-9973 $m Physiological research $n Physiol Res $x MED00003824
- LZP __
- $b NLK116 $a Pubmed-20240509