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血管抑制性类固醇和地塞米松对大鼠海绵植入物中血管生成和细胞因子水平的不同影响。

Differential effects of angiostatic steroids and dexamethasone on angiogenesis and cytokine levels in rat sponge implants.

作者信息

Hori Y, Hu D E, Yasui K, Smither R L, Gresham G A, Fan T P

机构信息

Department of Pharmacology, University of Cambridge.

出版信息

Br J Pharmacol. 1996 Aug;118(7):1584-91. doi: 10.1111/j.1476-5381.1996.tb15578.x.

Abstract
  1. Subcutaneous implantation of sterile polyether sponges elicited a reproducible neovascular response in rats, as determined by blood flow measurement with a 133Xe clearance technique and confirmed histologically. This model was used to monitor the levels of two cytokines during angiogenesis and to compare the activities of angiostatic steroids and anti-inflammatory steroids. 2. Initial experiments followed the neovascular development over a 20-day period. Daily local injection of hydrocortisone caused a dose-dependent (0.5, 5 and 50 micrograms per sponge) inhibition of the basal sponge-induced angiogenesis. However, daily systemic treatment of hydrocortisone (2, 10 and 50 mg kg-1, s.c.) was less effective at inhibiting angiogenesis, and this inhibition was not sustained by day 20 after sponge implantation. 3. To investigate the involvement of cytokines during the course of angiogenesis, we measured the endogenous levels of tumour necrosis factor-alpha (TNF-alpha) and interleukin 6 (IL-6) in sponge implants. Levels of IL-6 and TNF-alpha peaked at day 7 and day 11 after implantation, respectively. These cytokine levels subsided through the completion of angiogenesis by day 20. 4. Subsequent experiments were carried out over a 14-day period. Among the three angiostatic steroids tested, U-24067 (6 alpha-fluoro-17,21 - dihydroxy-16 alpha-methylpregna -4,9(11)-diene-3,20-dione-21-acetate) showed a dose-dependent inhibition (0.5, 5 and 50 micrograms per sponge per day) of sponge-induced angiogenesis. Tetrahydro-S was also effective at 5 micrograms doses, but medroxyprogesterone failed to affect the angiogenic response. None of these steroids caused atrophies of the spleen and thymus. 5. Daily local injection of dexamethasone (0.5 microgram per sponge) inhibited the basal sponge-induced angiogenesis almost completely. Although higher doses of dexamethasone (5 and 50 micrograms per sponge) did not produce further inhibition of angiogenesis, they caused severe spleen and thymus weight losses, indicative of immunosuppression. 6. At the daily dose of 5 micrograms per sponge, dexamethasone inhibited angiogenesis and produced a marked reduction in the levels of TNF-alpha and IL-6 at day 14. In contrast, hydrocortisone, U-24067 and tetrahydro-S did not influence the levels of TNF-alpha and IL-6. 7. We concluded that the anti-angiogenic activity of angiostatic steroids and anti-inflammatory steroids in the rat sponge model is independent of their ability to reduce the production of TNF-alpha and IL-6. The differential effects of angiostatic and anti-inflammatory steroids suggest that U-24067 and its derivatives may have therapeutic potential in the management of angiogenic diseases such as rheumatoid arthritis.
摘要
  1. 通过用¹³³Xe清除技术测量血流量并经组织学证实,在大鼠皮下植入无菌聚醚海绵可引发可重复的新生血管反应。该模型用于监测血管生成过程中两种细胞因子的水平,并比较血管抑制性类固醇和抗炎性类固醇的活性。2. 初始实验追踪了20天内的新生血管发育情况。每日局部注射氢化可的松对海绵诱导的基础血管生成产生剂量依赖性(每块海绵0.5、5和50微克)抑制。然而,每日全身给予氢化可的松(2、10和50毫克/千克,皮下注射)对血管生成的抑制效果较差,且在海绵植入后第20天这种抑制作用不再持续。3. 为研究细胞因子在血管生成过程中的作用,我们测量了海绵植入物中肿瘤坏死因子-α(TNF-α)和白细胞介素6(IL-6)的内源性水平。IL-6和TNF-α水平分别在植入后第7天和第11天达到峰值。这些细胞因子水平在第20天血管生成完成时下降。4. 后续实验在14天内进行。在所测试的三种血管抑制性类固醇中,U-24067(6α-氟-17,21-二羟基-16α-甲基孕甾-4,9(11)-二烯-3,20-二酮-21-乙酸酯)对海绵诱导的血管生成表现出剂量依赖性(每天每块海绵0.5、5和50微克)抑制。四氢-S在5微克剂量时也有效,但甲羟孕酮未能影响血管生成反应。这些类固醇均未导致脾脏和胸腺萎缩。5. 每日局部注射地塞米松(每块海绵0.5微克)几乎完全抑制了海绵诱导的基础血管生成。尽管更高剂量的地塞米松(每块海绵5和50微克)未进一步抑制血管生成,但它们导致脾脏和胸腺重量显著减轻,表明存在免疫抑制。6. 在每天每块海绵5微克的剂量下,地塞米松在第14天抑制了血管生成,并使TNF-α和IL-6水平显著降低。相比之下,氢化可的松、U-24067和四氢-S未影响TNF-α和IL-6水平。7. 我们得出结论,在大鼠海绵模型中,血管抑制性类固醇和抗炎性类固醇的抗血管生成活性与其降低TNF-α和IL-6产生的能力无关。血管抑制性和抗炎性类固醇的不同作用表明,U-24067及其衍生物在治疗类风湿关节炎等血管生成性疾病方面可能具有治疗潜力。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/638b/1909851/605ae73fda1a/brjpharm00086-0034-a.jpg

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