The sunscreening effect can be varied according to the vehicles. Therefore the purpose of this study is to compare the effect of vehicles(bases) on sun protection in p-aminobenzoic acid, cinnamate and benzophenone sunscreens with same concentration (2.5%), We included ointment (white petrolatum), cream (hydrophilic), milky lotion and alcohol as the sunscreen vehicles. The test results can be summarized as follows: We could not recognize a sunscreening effect of sunscreen vehicles which did not contain sunscreening agent. In the case of p-aminobenzoic acid, the mean sun protection factor was higher in the sequence of cream, milky lotion, alcohol, ointment, each showing 9, 95+/-3.67, 8.09+/-2.56, 5.14+/-1.45, 4.35+/-1.46 respectively. In the case of cinnamate, the mean sun protection factor was higher in the sequence of cream, ointment, milky lotion, alcohol, each showing 6 46+/-1.89, 5.42+/-1.49, 4.82+/-1.84, 4.05+/-1.45 respectively. 4. In the case of benzophenone, the mean sun protection factor was higher in the sequence of cream, alcohol, ointment, milky lotion, each showing 5 .26+/-1.56, 4.94+/-1.24, 4.56+/-1.71, 4.18+/-1.23 respectively.
4-Aminobenzoic Acid ; Skin* ; Solar System ; Sun Protection Factor ; Sunscreening Agents

Calcipotriol, a synthetic analogue of calcitriol(1,25-dihydroxyvitamin D) is as active as calcitriol in inducing cell differentiation and inhibiting cell pralifiration but at least 100 times less active than calcitriol in its effect on calcium metabolism. We report a case of psoriasis in a 28 year old male who was treated with calcipotriol ointment on the right forearm. The therapeutic effect of calcinoipotriol ointment was compared with desoxymethason, cream applied on the left forearm. Both topical agents reduced equally the degrees of scale, erythema and thickness of the lesions. We observed that the calcipotriol ointment was effective in the treatment of psoriasis n this case.
Adult ; Calcitriol ; Calcium ; Cell Differentiation ; Erythema ; Forearm ; Humans ; Male ; Metabolism ; Psoriasis*

The present study was undertaken to inveatigate whether contaet sensitivity was decreased or not in patients with atopic dermatitis, and to investigate phagocytic function of neutrophils in patients with atopic dermatitis. 1. Dinitrochlorobenzene (DNCB), a compound which uniformly induce hypersensitivity in normal individuals, had been used in the preaent study to investigate cutaneous anergy in 16 patients with atopic dermatitis. Sensitizing does of DNCB (2,000 microgram) was applied and examined at 7th and 14th day for a spontaneous flare. In the absence of spontaneous flare, challenge dose (50microgram) was reapplied and examined. Seven of the 16 cases (43.8%.) had positive reaction to DNCB. These result showed decreased contact sensitivity in patients with atopic dermatitis, which suggested some defect in the cell-mediated immunity in patients with atopic dermatitis. 2. There were some evidence that susceptibility to certain infection was increased in patients with atopic dermatitis. For investigating killing function in phagoeytosis of neutrophils in patients with atopic dermatitis, nitroblue tetrazolium dye reduction (NBT) and stimalated NBT test had performed in 35 cases of atopic dermatitis and 20 cases of healthy control. 1) There was no significant difference in the mean percentage and absolute number of NBT positive neutrophils between whole group of atopic dermatitis (8. 4+4. 9%, 301.2+225.6) and control group (6. 9+2. 9%, 246.2+143. 8). 2) The mean percentage and absolute number of stmulated NBT poeitive neutrophils in whole group of atopic dermatitis (19.6+7.3%, 702. 1+377. 2) did not differ significantly from control group (22.7+5.3%, 812.2+382.2). 3) There was no significant difference in the mean value of NBT aad stimulated NBT test in comparing the mild groud, moderate group and severe group with control group. These resuIts suggested that killing function in phagocytosis of neutrophils in patients with atopic dermatitis was not impaired.
Dermatitis, Atopic* ; Dermatitis, Contact ; Dinitrochlorobenzene* ; Homicide ; Humans ; Hypersensitivity ; Immunity, Cellular ; Neutrophils ; Nitroblue Tetrazolium ; Phagocytosis

BACKGROUND: The xenon arc solar simulator is the most commonly used light source in studies on immediate tanning, but there has been no report on the immediate tanning response in Korean skin induced by UVA from that source. OBJECTIVE: This study was conducted to measure the minimal immediate tanning dose(MITD) for UVA in Korean, brown skin. Methods: UVA irradiation was performed on normal back skin of twenty-six healthy Korean young adults, with increasing doses from 0.5J/cm2 to 4.5J/cm2 using xenon arc solar simulator equipped with appropriate filters. Visual assessment of MITD was done by two investigators. Results: The mean and standard deviations of MITD were 2.38+/- 0.65J/cm2 in 26 subjects. MITDs distributed from 1.0J/cm2 to 3.5J/cm2. There were no significant differences of MITD between skin type III and IV. Conclusion: Conclusively, we obtained the data on the MITD in Korean skin induced by UVA from the solar simulator. The results of this study may be valuable for the research into photomedicine and useful data for evaluating sunscreens.
Humans ; Research Personnel ; Skin ; Sunscreening Agents ; Tanning* ; Triacetoneamine-N-Oxyl* ; Xenon ; Young Adult*

Photosensitive psoriasis is a rare disease defined as psoriasis in which the lesions deteriorate or new lesions develop after sun exposure. It should be differentiated from other photosensitive conditions that may be a vated or confused on sun-exposure. Half of the patients have a history of polymorphic light eruption(PMLE), whieh several weeks later develops into psoriasis lesions and the others have no history of preceding PMLE reaction. PUVA therapy is recommended for the treatment of choice. In this report, we describe two cases of photosensitive psoriasis. A 51-year-old woman without underlying psoriasis suffered from erythemato-squamous papular lesions on the face, neck and dorsum of hands after sun-exposure. She revealed a lowered minimal erythema dose(MED) for UVA which was confused with a photosensitive disease. But characteristic psariatic plaques on the elbow, knee and palm and histologic findings made the diagnosis photosensitive psoriasis. She showed a good result to cyclosporine therapy. The other patient, a 44-year-old woman with underlying psoriasis, experienced an exacerbation with preceding PMLE and showed a lowered erythema threshold for UVB. She was treated with sun-screen and topical corticosteroids.
Adrenal Cortex Hormones ; Adult ; Cyclosporine ; Diagnosis ; Elbow ; Erythema ; Female ; Hand ; Humans ; Knee ; Middle Aged ; Neck ; Psoriasis ; PUVA Therapy ; Rare Diseases ; Solar System

In this experiment 40 adult male C57BL mice were used. The one ear of each animal was irradiated with high pressure mercury lamp (Burdick'UV-800) and the other ear was covered with nontransparent tape. Using split epidermal sheets treated with DOPA solution, a quatitiative study of epidermal melanocyte was carried out from the exposed and the shielded ear continuously on every second day during 14 daily exposures to 100 mJ/cm of UVB. The results were as follows : 1. Repeated radiation with ultraviolet light elicited a significant increase in population of melanocytes and the possible mechanism is a direct replication of the functioning melanocytes. 2. UVB irradiation induced increase in the number of epidermal melanocytes in covered ear as well as in irradiated ear. It is suggested that the population increase in the shielded skin is initiated by one or more systemic factors originating from the UVB irradiated skin.
Adult ; Animals ; Dihydroxyphenylalanine ; Ear* ; Humans ; Male ; Melanocytes* ; Mice ; Mice, Inbred C57BL* ; Skin ; Ultraviolet Rays

This study was undertaken to investigate the quantitative change of sunburn cell(FiBC)production and ear swelling reaction(ESR)aecording to the UVA radiation dose and time course sfter PUVA treatment. A total of 75 ICR male albino haired mice were used as subjects. The results were as follows : 1. At 24 hours after PUVA treatment, the mean SBC numbers per cm length of epidermis were 29.1+13.6 with 1J/cm, 48.8+19.5 with 5J/cm, and 51.6+14. 8 with 10J/cm of UVA irradiation. SBC production was dose related with respect to radiation dose, but the increment was not so remarkable with more than 5J /cm of UVA irradiation. 2. [n PUVA treatment using 5J/cm of UVA, the mean SBC numbers per cm length of epiderrnis were 48.8+19.5 after 24 hours, 63.8+18.3 after 48 hours. SBC numbers rose to a maximum at 48 hours, but epidermal damage precludecl SBC counting after this. 3. At, 24 hours after PUVA treatment, no significant ESR was observed with 1 an3 5J/cm of UVA. In PUVA treatment using lOJ/cm of UVA, the mean ear thickness was 20.6+1.7( x 10mm) before treatment and 30.1+3.3( x 10mm') at 2h: hours after treatment, which showed significa.nt change(p<0.05). 4. In PUVA treatment using 5J(cm of UVA, ESR showed significant change at 43hours reaching a maximum at 72 hours. After 7 days, ESR was not measurable due to ear necrosis.
Animals ; Ear* ; Epidermis ; Hair ; Humans ; Male ; Mice* ; Necrosis ; Skin* ; Sunburn*

BACKGROUND: The action of ultraviolet rays on DNA causes the main photobiologic response of cells to ultraviolet rays. To study this effect, tritiated thymidine autoradiography was used. Recently 5-bromo-2deoxyuridine(BrdU), an analogue of thymidine, immunohistochemistry has been developed and is used in the detection of synthetic phase cells. Compared to autoradiography, there are several advantages of BrdU immunohistochemistry; a shorter processing time, no requirement of specific facilites. PUVA, the combination method of UVA and Psoralen has lots of photobiologic effects. OBJECTIVE: Using Brdu immunohistochemistry, the effect of PUVA on the DNA synthesis of tape stripped mouse epdermis was studied. METHOD: Mice stripped by adhesive tape for enhancing DNA synthesis were injected intraperitoneally with 50mg/kg of BrdU immediately after stripping and at 6, 12, 14, 16, 18, 20, 22, 24 and 48 hours after tape stripping for decision of the time for PUVA. The skin diopsies were taken and the specimens were stained by BrdU immunohistochemistry. Single systemic PUVA exposure was performed on the stripped epidermis in peak synthetic time after tape stripping. The irradiation dose of UVA was 5J/cm(2). 8-MOP was administered at 90 minutes before UVA irradiation via a feeding tube with the dose of 16mg/kg. Mice were injected intraperitoneally with 50mg/kg of BrdU immediately after PUVA and at 12, 24, 48, 72 hours, and 7 days after PUVA. The skin biopsies were taken and the specimens were stained by BrdU immunohistochemistry. Positively labeled cells were counted per 5mm epidermis. RESULT: The results can be summerized as follows : 1. The mean numbers of BrdU labeled cells of each groups according to time after tape stripping were 11.0+/-4.4 at immediate, 24.0+/-9.7 at 6 hours 31.4+/-18.1 at 12 hours, 55.0+/-16.1 at 14 hors, 25.8+/-9.7 at 16 hors, 44.2+/-15.7 at 18 hors, 47.6+/-15.6 at 20 hors, 33.4+/-12.3 at 22 hors, 38.0+/-16.3 at 24 hors, and 22.0+/-8.2 at 48 hors group. The mean number of BrdU labeled cells was observed at 14 hors after tape stripping (p<0.05). So by tape stripping DNA synthesis was enhanced maximally at 14 hours after tape stripping. 2. The man numbers of BrdU labeled cells of each groups according to time after PUVA were 11.0+/-7.5 at immediate, 32.2+/-13.2 at immediate, 32.2+/-13.2 at 6hors, 26.4+/-13.4 at 24 hours, 18.0+/-3.4 at 48 hours, 40.3+/-8.3 at 72 hours, and 27.8+/-11.0 at 7 days group. The lowest number of BrdU labeled cells was observed immediately after PUVA(p<0.05). The decreasein the number of BrdU labeled cells significantly persisted 48 hours after PUVA(p<0.05). CONCLUSION: The inhibitory effect on DNA synthesis of PUVA might be sustained 48 hours after PUVA. DNA synthesis was recovered at 72 hours after PUVA and sustained for 7 days.
Adhesives ; Animals ; Autoradiography ; Biopsy ; Bromodeoxyuridine ; DNA* ; Epidermis ; Ficusin ; Immunohistochemistry* ; Methoxsalen ; Mice ; Skin ; Thymidine ; Ultraviolet Rays

This study was done to study the effect of UVA radiation upon sunburn cell formation by UVB. In this study a total of 67 ICR male albino haired mice were used. The results were as follows: 1. UVA radiation produce a little or no sunburn cell in doses 5 J/cm(2), 10 J/cm(2), and 15 J/cm(2). 2. Preirradiation of UVA 5 J/cm, 10 J/cm(2), 15 J/cm(2) had no effect on the sunburn cell formation by UVB 20 mJ/cm(2), 80 mj/cm(2)
Animals ; Hair ; Humans ; Male ; Mice ; Sunburn*

No abstract available.
DNA* ; Humans* ; Lymphocytes*