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体内激光小梁成形术后猫小梁网中的 DNA 复制。

DNA replication in the cat trabecular meshwork after laser trabeculoplasty in vivo.

机构信息

Departments of Ophthalmology and Biochemistry and Molecular Biology, Casey Eye Institute, Oregon Health Sciences University; and Department of Ophthalmology, Devers Eye Institute, Good Samaritan Hospital, Portland, Oregon, U.S.A.

出版信息

J Glaucoma. 1994 Spring;3(1):36-43.

Abstract

The in vivo response to laser trabeculoplasty (LTP) was evaluated by measuring the incorporation of thymidine into DNA in the nuclei of trabecular meshwork cells. incorporation into DNA was analyzed by light microscopic autoradiography and by scintillation counting of trabecular extracts. Sixteen cats received argon LTP at a power setting of either 0.3 or 1.0 watt with the contralateral eye serving as a control; a 48-h exposure to HT began 1, 5, or 12 days later. The level of HT incorporation into DNA for LTP-treated eyes was significantly higher than controls for the earliest labeling period, but not at the later time points. This pattern was observed for both 0.3-and 1.0-watt treatments. In a second experiment, LTP was performed on six animals; a power setting of 0.3 watt was used in the left eye, and a power setting of 1 watt was used in the right eye. All 12 eyes were radiolabeled for 48 h with HT beginning 1 day after LTP. A small but significant difference in incorporation levels was found between these two power settings. Trabecular cell division may play a role in the therapeutic efficacy of LTP in glaucoma patients.

摘要

通过测量激光小梁成形术(LTP)后小梁网细胞核内胸腺嘧啶核苷掺入 DNA 的情况,评估体内的反应。通过光镜放射自显影术和小梁提取物闪烁计数分析掺入 DNA 的情况。16 只猫的双眼分别接受功率设置为 0.3 或 1.0 瓦特的氩激光 LTP 治疗,对侧眼作为对照;48 小时后开始接触 HT,时间分别为 1、5 或 12 天。对于最早的标记期,LTP 治疗眼的 HT 掺入 DNA 的水平明显高于对照,但在较晚的时间点则不然。这一模式在 0.3 和 1.0 瓦特两种处理方式中均有观察到。在第二项实验中,对 6 只动物进行了 LTP 治疗;左眼使用 0.3 瓦特的功率设置,右眼使用 1 瓦特的功率设置。所有 12 只眼在 LTP 后 1 天开始用 HT 进行 48 小时放射性标记。在这两个功率设置之间发现了一个微小但显著的掺入水平差异。小梁细胞分裂可能在青光眼患者的 LTP 治疗效果中起作用。

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