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氢化可的松、丁酸氢化可的松和倍他米松对人皮肤体内胶原蛋白合成影响的比较。

Comparison of the effect of hydrocortisone, hydrocortisone-17-butyrate and betamethasone on collagen synthesis in human skin in vivo.

作者信息

Haapasaari K M, Risteli J, Koivukangas V, Oikarinen A

机构信息

Department of Dermatology, University of Oulu, Finland.

出版信息

Acta Derm Venereol. 1995 Jul;75(4):269-71. doi: 10.2340/0001555575269271.

Abstract

It has been shown previously that topical corticosteroid treatment decreases collagen synthesis in human skin in vivo and that the adverse effects are due to reduced collagen synthesis. The aim of the present study was to evaluate the effect of hydrocortisone, hydrocortisone-17-butyrate and betamethasone on collagen synthesis in human skin in vivo. Fourteen healthy male volunteers applied hydrocortisone, hydrocortisone-17-butyrate, betamethasone and vehicle twice a day for one week to four separate areas marked on their abdominal skin. The collagen synthesis rate in the skin was measured by assaying collagen propeptides from the suction blisters induced on the treated areas. Aminoterminal propeptide of type I procollagen (PINP) and aminoterminal propeptide of type III procollagen (PIIINP) were measured from skin blister fluid using radioimmunoassays. Skin thickness was measured with ultrasound. Hydrocortisone decreased the two propeptides studied in the suction blister fluids less than did hydrocortisone-17-butyrate and betamethasone, but the interindividual variation was great. Hydrocortisone-17-butyrate and betamethasone had almost similar decreasing effects on the propeptides in the suction blister fluid. Hydrocortisone decreased the concentrations of PINP and PIIINP by about 35%. In some subjects (4/14) the decline of the collagen propeptide levels was over 50%. The decline in the concentration of PINP was 63% by hydrocortisone-17-butyrate and 69% by betamethasone, while the decrease in PIIINP was 55% by hydrocortisone-17-butyrate and 62% by betamethasone. None of the treatments had any effect on skin thickness within one week. In conclusion, it seems that hydrocortisone is less atrophogenic than hydrocortisone-17-butyrate and betamethasone, as shown by radioimmunoassays for collagen propeptides. The order of inhibitory potency of the three glucocorticoids on collagen synthesis was hydrocortisone < hydrocortisone-17-butyrate < betamethasone. Thus, assay of collagen propeptides from suction blisters can be used to screen various steroids with respect to their action on collagen synthesis.

摘要

先前的研究表明,局部应用皮质类固醇治疗可降低人体皮肤体内的胶原蛋白合成,且其不良反应是由于胶原蛋白合成减少所致。本研究的目的是评估氢化可的松、氢化可的松 -17-丁酸酯和倍他米松对人体皮肤体内胶原蛋白合成的影响。14名健康男性志愿者在腹部皮肤上标记的四个不同区域,每天两次涂抹氢化可的松、氢化可的松 -17-丁酸酯、倍他米松和赋形剂,持续一周。通过测定治疗区域诱导产生的抽吸水疱中的胶原蛋白前肽来测量皮肤中的胶原蛋白合成率。使用放射免疫分析法从皮肤水疱液中测量I型前胶原氨基端前肽(PINP)和III型前胶原氨基端前肽(PIIINP)。用超声测量皮肤厚度。氢化可的松使抽吸水疱液中所研究的两种前肽的降低程度小于氢化可的松 -17-丁酸酯和倍他米松,但个体间差异很大。氢化可的松 -17-丁酸酯和倍他米松对抽吸水疱液中的前肽具有几乎相似的降低作用。氢化可的松使PINP和PIIINP的浓度降低约35%。在一些受试者(4/14)中,胶原蛋白前肽水平的下降超过50%。氢化可的松 -17-丁酸酯使PINP浓度下降63%,倍他米松使PINP浓度下降69%,而氢化可的松 -17-丁酸酯使PIIINP下降55%,倍他米松使PIIINP下降62%。在一周内,所有治疗对皮肤厚度均无任何影响。总之,如通过胶原蛋白前肽的放射免疫分析所示,氢化可的松的致萎缩性似乎低于氢化可的松 -17-丁酸酯和倍他米松。三种糖皮质激素对胶原蛋白合成的抑制效力顺序为氢化可的松<氢化可的松 -17-丁酸酯<倍他米松。因此,从抽吸水疱中检测胶原蛋白前肽可用于筛选各种类固醇对胶原蛋白合成的作用。

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