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皮质醇对器官培养中猪关节组织的影响。

The effect of cortisol on porcine articular tissues in organ culture.

作者信息

Tyler J A, Fell H B, Lawrence C E

出版信息

J Pathol. 1982 Aug;137(4):335-51. doi: 10.1002/path.1711370408.

Abstract

(1) The effects of hydrocortisone succinate (1.0--0.01 micrograms HC/ml of medium) on porcine articular tissues in organ culture have been studied by histological and biochemical methods. (2) 1.0 and 0.1 micrograms HC/ml considerably inhibited the severe breakdown of matrix that occurs in living and dead cartilage explained in contact with synovial tissue. (3) The depletion of matrix in living cartilage cultivated in the same dish as but not in contact with synovial tissue, is much diminished when the medium contains 1.0 or 0.1 micrograms HC/ml. (4) Cartilage grown in the used medium of synovial tissue loses both proteoglycan and hydroxyproline; the addition of HC to the used medium has little (1.0 microgram HC/ml) or 0.1 microgram HC/ml) no inhibitory effect. If, however, the used medium is from synovial tissue that has been cultured in the presence of 1.0 or 0.1 micrograms HC/ml, loss of proteoglycan and collagen from the cartilage is much reduced. (5) In isolated cartilage in normal medium there is outgrowth of cells from the cut surface and some loss of proteoglycan and collagen; outgrowth is completely, and loss of matrix components partially suppressed by 1.0 micrograms HC/ml. (6) Isolated synovial tissue cultured in normal medium shrinks to about one-third of its original size, loses much of its collagen and secretes neutral metallo-proteinases into the medium; in the presence of 1.0 microgram HC/ml these changes are largely prevented. The explants also secrete an inhibitor of metallo-proteinases the production of which is not reduced by HC.

摘要

(1) 采用组织学和生物化学方法,研究了琥珀酸氢化可的松(1.0 - 0.01微克氢化可的松/毫升培养基)对器官培养的猪关节组织的影响。(2) 1.0微克/毫升和0.1微克/毫升的氢化可的松显著抑制了与滑膜组织接触的活软骨和死软骨中发生的基质严重降解。(3) 当培养基中含有1.0微克/毫升或0.1微克/毫升时,与滑膜组织在同一培养皿中培养但不接触的活软骨中的基质消耗显著减少。(4) 在滑膜组织用过的培养基中生长的软骨会同时失去蛋白聚糖和羟脯氨酸;向用过的培养基中添加氢化可的松(1.0微克/毫升)几乎没有抑制作用,添加0.1微克/毫升则没有抑制作用。然而,如果用过的培养基来自在1.0微克/毫升或0.1微克/毫升氢化可的松存在下培养的滑膜组织,软骨中蛋白聚糖和胶原蛋白的损失会大大减少。(5) 在正常培养基中培养的分离软骨,从切割表面有细胞生长,并且有一些蛋白聚糖和胶原蛋白的损失;1.0微克/毫升的氢化可的松完全抑制了细胞生长,部分抑制了基质成分的损失。(6) 在正常培养基中培养的分离滑膜组织收缩至其原始大小的约三分之一,失去大量胶原蛋白,并向培养基中分泌中性金属蛋白酶;在1.0微克/毫升氢化可的松存在下,这些变化在很大程度上得到了预防。外植体还分泌金属蛋白酶抑制剂,其产生不受氢化可的松的影响。

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