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Dive into the research topics where John C. Dowdy is active.

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Featured researches published by John C. Dowdy.


Photochemistry and Photobiology | 2004

Unexpected Photolysis of the Sunscreen Octinoxate in the Presence of the Sunscreen Avobenzone

Robert M. Sayre; John C. Dowdy; Andre J. Gerwig; William J. Shields; Roger V. Lloyd

Abstract A major concern raised about photostability studies of sunscreen products is that the photodegradation of sunscreens does not readily translate into changes in product performance. This study examines the correlation between photochemical degradation of sunscreen agents and changes in protection provided by sunscreen films. Films of a commercial sunscreen product containing avobenzone, oxybenzone and octinoxate were irradiated using a fluorescent UV-A phototherapy lamp with additional UV-B blocking filter. Periodically, during irradiation the transmittances of the films were measured and samples collected for chemical analysis of the sunscreen agents using high-performance liquid chromatography techniques. The results show that UV-induced changes in UV transmittance of sunscreen films correlate with changes in concentration of sunscreen agents. In a parallel experiment, we also irradiated a thin film of the same product in the cavity of an electron spin resonance (ESR) spectrometer. We report the concomitant photolysis of avobenzone and octinoxate that predominates over expected E/Z photoisomerization and that irradiation of a film of this product produced free radicals detected by ESR spectroscopy that persisted even after exposure had ended.


Metabolism-clinical and Experimental | 2008

25-Hydroxyvitamin D, cholesterol, and ultraviolet irradiation

Laura D. Carbone; E. William Rosenberg; Elizabeth A. Tolley; Michael F. Holick; Thomas A. Hughes; Mitchell A. Watsky; Karen D. Barrow; Tai C. Chen; Nathaniel K. Wilkin; Syamal K. Bhattacharya; John C. Dowdy; Robert M. Sayre; Karl T. Weber

Vitamin D deficiency may have implications for cardiovascular health. The purpose of this study was to determine the relationship of 25-hydroxyvitamin D (25[OH]D) to cholesterol and lipoprotein particles and to determine whether increasing 25(OH)D through ultraviolet (UV) irradiation impacted on these parameters in healthy young men and women. This was a randomized trial of 51 adults exposed to suberythemal doses of whole-body irradiation using UV lamps that emitted UV-A and UV-B radiation, compared with a control group, twice weekly for 12 weeks. 25-Hydroxyvitamin D, cholesterol, and lipoprotein subfractions were measured at baseline and after 12 weeks. There was a significant (P < .03) positive association between 25(OH)D and apolipoprotein A-I (Apo A-I) and lipoprotein A-I (Lp A-I). The ratio of low-density lipoprotein to high-density lipoprotein was significantly (P < or = .044) negatively correlated with 25(OH)D levels. The levels of 25(OH)D increased significantly in the treated compared with control group (P < .05). Overall, there were no significant differences between the treated and control groups in any lipoproteins or apolipoproteins after administration of UV irradiation. Subgroup analysis for Apo A-II confined to those with 25(OH)D insufficiency (25[OH]D <75 nmol/L [30 ng/mL]) revealed decreases in Apo A-II in the treated group and increases in the control group that were statistically significantly different between the groups (P = .026). We found a significant positive correlation between 25(OH)D and Apo A-I and Lp A-I and a significant negative correlation between 25(OH)D and the ratio of low-density lipoprotein to high-density lipoprotein. In those with vitamin D insufficiency, we found small decreases in Apo A-II in the treated relative to the control group. Overall, though, twice weekly exposure to UV radiation resulting in an increase in serum 25(OH)D had no significant impact on lipoprotein composition.


British Journal of Dermatology | 2013

Ultraviolet radiation regulates cortisol activity in a waveband dependent manner in human skin ex-vivo

Cezary Skobowiat; Robert M. Sayre; John C. Dowdy; Andrzej Slominski

Background  11β‐Hydroxysteroid dehydrogenase type 1 (11β‐HSD1), 11β‐hydroxysteroid dehydrogenase type 2 (11β‐HSD2), and glucocorticoids (GC) and their receptor (GR) play a key role in tissue‐specific regulation of GC action.


Photochemistry and Photobiology | 2007

Darkness at Noon: Sunscreens and Vitamin D3

Robert M. Sayre; John C. Dowdy

We are assured by responsible scientific and governmental organizations that sunscreens should be routinely worn to reduce skin cancer risk. We are also advised that wearing sunscreens will not hinder our ability to produce sufficient previtamin D3 (preD3) from casual sunlight exposure. We report the examination of a series of 166 solar spectra, obtained on different days throughout a year, evaluated for erythemic and preD3 effectiveness and the relative effects of recommended Sun protection factor (SPF) 15 sunscreen. The results show that the sunscreen is much more effective in blocking the formation of preD3, than its labeled SPF for preventing sunburn. In fact with sunscreen applied only miniscule amounts of preD3 are predicted to be made outdoors even with extensive exposure. This raises important questions regarding the safest way to use sunlight exposure to promote healthy vitamin D3 levels and suggests the need to modify the public safety “Safe Sun” messages.


Photochemistry and Photobiology | 2004

Dermatological Risk of Indoor Ultraviolet Exposure from Contemporary Lighting Sources

Robert M. Sayre; John C. Dowdy; Maureen Poh-Fitzpatrick

Abstract Discussions of risks and implications of cutaneous exposure to indoor lighting, including hypothetical contribution to causality of melanoma, have mainly concentrated on ultraviolet (UV) A and B (UVA, UVB) spectral emissions from fluorescent bulbs. Only studies of quartz halogen lamps have suggested that users might sustain UVC-induced injury. Examination of light sources in the home and school of a child with xeroderma pigmentosum revealed that several different types emitted surprising levels of UV. Our purpose was to assess the extent of UV emissions from a variety of commonly used light sources to identify potential dermatological risks. UV and visible spectral emissions of commercially obtained lamps of several types were measured using a calibrated spectral radiometer traceable to the National Institute of Standards and Technology. Indoor light sources including fluorescent, quartz halogen and even tungsten filament incandescent lamps provided UVA, UVB and sometimes UVC emissions. Intensities of some emissions were of similar magnitude to those in sunlight. Chronic exposure to indoor lighting may deliver unexpected cumulative UV exposure to the skin and eyes. Patients with UV-exacerbated dermatoses should be cautioned about potential adverse reactions from indoor lighting.


The Journal of Steroid Biochemistry and Molecular Biology | 2010

Holick's rule and vitamin D from sunlight.

John C. Dowdy; Robert M. Sayre; Michael F. Holick

Holicks rule says that sun exposure 1/4 of a minimal erythemal dose (MED) over 1/4 of a body is equivalent to 1000 International Units (IU) oral vitamin D3. Webb and Engelsen recently commented that the ultraviolet (UV) spectrum used to establish Holicks rule is unknown. They consequently used a spring midday Boston solar spectrum to estimate ample sunlight exposures for previtamin D3 (preD3) at various locations. Literature review found the source upon which this rule is based was a fluorescent sunlamp (FS lamp). The FS spectrum is known and its relative weighting against the action spectra for erythema and the preD3 is significantly different from the solar spectrum used to derive the standard vitamin D effective dose (SDD). The preD3 effectiveness of the solar spectrum per unit erythemal hazard is greater than the FS lamp by a factor of 1.32. Consequently, UV exposure estimates based on Boston reference sunlight, instead of the UV lamp employed in the originating experiments, over estimate UV exposure equivalent to approximately 1000 IU orally by approximately 1/3. This redefinition of SDD impacts risk/benefit assessments of optimal/feasible sun exposure for vitamin D maintenance and the application of Holicks rule to rational public health messages.


Autoimmunity Reviews | 2009

The risk of ultraviolet radiation exposure from indoor lamps in lupus erythematosus

Rachel S. Klein; Robert M. Sayre; John C. Dowdy; Victoria P. Werth

It is well known that ultraviolet radiation can exacerbate skin disease in patients with lupus erythematosus. While many patients are advised to avoid sunlight and artificial tanning, it is not clear how best to counsel patients regarding the use of indoor lamps. Indeed, many of the light bulbs commonly used in the home and workplace emit low-dose ultraviolet radiation. The irradiance is considerably lower than that of the sun, however the exposure time can last for hours and is typically repeated on a daily basis. Therefore, it is possible that this chronic exposure could ultimately result in a significant accumulation of damage.


Photochemistry and Photobiology | 2009

Analysis of Compact Fluorescent Lights for Use by Patients with Photosensitive Conditions

Rachel S. Klein; Victoria P. Werth; John C. Dowdy; Robert M. Sayre

Ultraviolet radiation (UVR) is hazardous to patients with photosensitive skin disorders, such as lupus erythematosus, xeroderma pigmentosum and skin cancer. As such, these patients are advised to minimize their exposure to UVR. Classically, this is accomplished through careful avoidance of sun exposure and artificial tanning booths. Indoor light bulbs, however, are generally not considered to pose significant UVR hazard. We sought to test this notion by measuring the UV emissions of 19 different compact fluorescent light bulbs. The ability to induce skin damage was assessed with the CIE erythema action spectrum, ANSI S(λ) generalized UV hazard spectrum and the CIE photocarcinogenesis action spectrum. The results indicate that there is a great deal of variation amongst different bulbs, even within the same class. Although the irradiance of any given bulb is low, the possible daily exposure time is rather lengthy. This results in potential daily UVR doses ranging from 0.1 to 625 mJ cm−2, including a daily UVB (290–320 nm) dose of 0.01 to 15 mJ cm−2. Because patients are exposed continually over long time frames, this could lead to significant cumulative damage. It would therefore be prudent for patients to use bulbs with the lowest UV irradiance.


Photodermatology, Photoimmunology and Photomedicine | 2001

Effect of UV irradiation on type I collagen fibril formation in neutral collagen solutions

Julian M. Menter; Abrienne M. Patta; Robert M. Sayre; John C. Dowdy; Isaac Willis

Background: Collagens have the well‐known ability to spontaneously self‐associate to form fibrils at physiological temperature and neutral pH in vitro and in vivo. Because solar UV may photochemically alter collagen, the kinetics of fibril formation may be modified. Thus, we have begun a systematic study of the effect of various UV wavebands on fibril formation.


Photodermatology, Photoimmunology and Photomedicine | 2003

Uniformity of sunscreen product application: a problem in testing, a problem for consumers

Dennis L. Lott; Joseph W. Stanfield; Robert M. Sayre; John C. Dowdy

Background/Aims: Testing of sunscreen products requires application of uniform films of product of defined thickness to test volunteers. In spite of the seeming importance of product application to defining sunscreen efficacy, there have been few studies determining how well uniformity is achieved. The purpose of this work was to evaluate the uniformity of sunscreen products of different sun protection factors (SPFs) and vehicles on a variety of substrates by in vitro testing techniques. The results of a variety of testing strategies are reported.

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Andrzej Slominski

University of Alabama at Birmingham

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E. William Rosenberg

University of Tennessee Health Science Center

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Abrienne M. Patta

Morehouse School of Medicine

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Cezary Skobowiat

University of Tennessee Health Science Center

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Isaac Willis

Morehouse School of Medicine

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Julian M. Menter

Morehouse School of Medicine

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Karl T. Weber

University of Tennessee Health Science Center

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