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KH 1060(一种强效的1,25 - 二羟基维生素D3的20 - 表类似物)对糖皮质激素诱导的表皮和真皮萎缩的抑制作用

Inhibition of glucocorticoid-induced epidermal and dermal atrophy with KH 1060--a potent 20-epi analogue of 1,25-dihydroxyvitamin D3.

作者信息

Gniadecki R, Gniadecka M, Serup J

机构信息

Department of Dermatological Research, Leo Pharmaceutical Products, Ballerup, Denmark.

出版信息

Br J Pharmacol. 1994 Oct;113(2):439-44. doi: 10.1111/j.1476-5381.1994.tb17008.x.

DOI:10.1111/j.1476-5381.1994.tb17008.x
PMID:7834193
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1510095/
Abstract
  1. The possibility of preventing and treating glucocorticoid-induced skin atrophy with KH 1060 (the potent 20-epi-22-oxa-24a-homo-26,27-dimethyl analogue of 1,25-dihydroxyvitamin D3) was examined in a hairless mouse model. 2. KH 1060 (0.625-6.25 pmol cm-2 of skin) applied topically for 7 days together with 2.5 nmol cm-2 betamethasone-17-valerate prevented, in a concentration-dependent manner, the development of epidermal, dermal and total skin thinning caused by the glucocorticoid. The effect of KH 1060 on the epidermis occurred at a lower dose than on the dermis, and at doses above 1.25 pmol cm-2 KH 1060 caused epidermal hyperplasia. 3. KH 1060 (2.5 pmol cm-2) prevented the development of betamethasone-associated skin atrophy in mice during a long-term (4 weeks) treatment, and reversed established cutaneous glucocorticoid atrophy. 4. Radiolabelling experiments with [35S]-sulphate and [3H]-proline in vivo revealed that KH 1060 stimulated the synthesis of sulphated glycosaminoglycans and hydroxyproline in skin treated with betamethasone. 5. These findings strongly suggest that KH 1060 prevents and reverses glucocorticoid-induced skin atrophy by stimulating epidermal proliferation and enhancing synthesis of extracellular matrix in the dermis.
摘要
  1. 在无毛小鼠模型中研究了用KH 1060(1,25 - 二羟基维生素D3的强效20 - 表 - 22 - 氧杂 - 24a - 高 - 26,27 - 二甲基类似物)预防和治疗糖皮质激素诱导的皮肤萎缩的可能性。2. 将KH 1060(0.625 - 6.25 pmol/cm²皮肤)局部应用7天,与2.5 nmol/cm²的倍他米松 - 17 - 戊酸酯一起,以浓度依赖的方式预防了糖皮质激素引起的表皮、真皮和全层皮肤变薄。KH 1060对表皮的作用在比真皮更低的剂量下出现,并且在剂量高于1.25 pmol/cm²时,KH 1060引起表皮增生。3. 在长期(4周)治疗期间,KH 1060(2.5 pmol/cm²)预防了小鼠中倍他米松相关的皮肤萎缩,并逆转了已形成的皮肤糖皮质激素萎缩。4. 体内用[35S] - 硫酸盐和[3H] - 脯氨酸进行的放射性标记实验表明,KH 1060刺激了用倍他米松处理的皮肤中硫酸化糖胺聚糖和羟脯氨酸的合成。5. 这些发现强烈表明,KH 1060通过刺激表皮增殖和增强真皮中细胞外基质的合成来预防和逆转糖皮质激素诱导的皮肤萎缩。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6407/1510095/6642edb4dbc7/brjpharm00171-0118-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6407/1510095/6642edb4dbc7/brjpharm00171-0118-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6407/1510095/6642edb4dbc7/brjpharm00171-0118-a.jpg

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