Photoisomerization spectrum of urocanic acid in human skin and in vitro: effects of simulated solar and artificial ultraviolet radiation

2010 ◽  
Vol 132 (6) ◽  
pp. 884-891 ◽  
Author(s):  
A. KAMMEYER ◽  
M.B.M. TEUNISSEN ◽  
S. PAVEL ◽  
M.A. RIE ◽  
J.D. BOS
Biomaterials ◽  
1998 ◽  
Vol 19 (10) ◽  
pp. 897-903 ◽  
Author(s):  
Silvia Trasciatti ◽  
Adriano Podestà ◽  
Silvano Bonaretti ◽  
Viviano Mazzoncini ◽  
Sergio Rosini

1994 ◽  
Vol 29 (3) ◽  
pp. 396-397
Author(s):  
W.H.M.Craane-van Hinsberg ◽  
L. Bax ◽  
N.H.M. Flinterman ◽  
J. Verhoef ◽  
H.E. Junginger ◽  
...  

1994 ◽  
Vol 2 (1-2) ◽  
pp. 182
Author(s):  
W.H.M. Craane-van Hinsberg ◽  
F. Spies ◽  
G.S. Gooris ◽  
J.A. Bouwstra ◽  
J.C. Verhoef ◽  
...  

1966 ◽  
Vol 44 (6) ◽  
pp. 801-808 ◽  
Author(s):  
A. Kahlenberg ◽  
N. Kalant

The in vitro effects of insulin on glucose transport and dissimilation were studied in human skin. Slices of skin obtained post-mortem were incubated in phosphate and bicarbonate media with a glucose concentration of 5.6 mM. In both buffers, insulin increased the glucose uptake in non-diabetic skin without affecting the intracellular glucose content. Similar results were obtained for diabetic skin incubated in a phosphate buffer.In bicarbonate buffer, the basal rate of glucose utilization of skin from diabetics was lower than normal; this may have been the result of a defect in the phosphofructokinase reaction. Diabetic skin also had an increased responsiveness to insulin in bicarbonate buffer.Non-diabetic skin incubated in phosphate buffer had a lower basal rate of glucose uptake and a greater responsiveness to insulin than the same tissue incubated in bicarbonate buffer.It is concluded that (a) skin from diabetic humans incubated in bicarbonate buffer had a decreased basal rate of glucose utilization and increased responsiveness to insulin; (b) insulin stimulated both glucose transport and dissimilation in diabetic and non-diabetic human skin.


Author(s):  
L.X. Oakford ◽  
S.D. Dimitrijevich ◽  
R. Gracy

In intact skin the epidermal layer is a dynamic tissue component which is maintained by a basal layer of mitotically active cells. The protective upper epidermis, the stratum corneum, is generated by differentiation of the suprabasal keratinocytes which eventually desquamate as anuclear comeocytes. A similar sequence of events is observed in vitro in the non-contracting human skin equivalent (HSE) which was developed in this lab (1). As a part of the definition process for this model of living skin we are examining its ultrastructural features. Since desmosomes are important in maintaining cell-cell interactions in stratified epithelia their distribution in HSE was examined.


Sign in / Sign up

Export Citation Format

Share Document