Kim Jae Woo
Department of Ophthalmology, Catholic University of Daegu College of Medicine, Nam-gu, Daegu, Korea.
Korean J Ophthalmol. 2007 Mar;21(1):39-44. doi: 10.3341/kjo.2007.21.1.39.
To investigate the effect of insulin on the production of nitric oxide (NO) in the trabecular meshwork (TM) cells and the enzymatic synthetic pathway of tetrahydrobiopterin (BH(4)) synthesis.
Primarily cultured human TM cells were exposed to 1, 10, and 100 microgram/ml of insulin and 0, 1, 10, 100 and 1000 nM dexamethasone for 3 days. To evaluate the enzymatic pathway of BH(4) synthesis, 10 microM dexamethasone, 5 mM diaminopyrimidinone, 100 microM ascorbic acid, 100 microM sepiapterin, or 10 microM methotrexate were also co-administered respectively. Cellular survival and NO production were measured with MTT and Griess assay.
Insulin enhanced NO production in a dose-dependent manner significantly (0.05) without affecting cell viability, whereas dexamethasone inhibited NO production. With co-exposure of insulin, diaminopyrimidinone and sepiapterin inhibited insulin-induced NO production. Ascorbic acid increased NO production independent of insulin and methotrexate did not affect to the action of insulin in NO production.
Insulin increases NO production in TM cells via de novo synthetic pathway for BH(4) synthesis. Insulin could be involved in the regulation of trabecular outflow by enhancing NO production in TM cells.
研究胰岛素对小梁网(TM)细胞中一氧化氮(NO)生成及四氢生物蝶呤(BH(4))合成的酶促合成途径的影响。
将原代培养的人TM细胞分别暴露于1、10和100微克/毫升的胰岛素以及0、1、10、100和1000纳摩尔/升的地塞米松中3天。为评估BH(4)合成的酶促途径,还分别联合给予10微摩尔/升地塞米松、5毫摩尔/升二氨基嘧啶酮、100微摩尔/升抗坏血酸、100微摩尔/升蝶酰三谷氨酸或10微摩尔/升甲氨蝶呤。用MTT法和Griess法测定细胞存活率和NO生成量。
胰岛素以剂量依赖性方式显著增强NO生成(P<0.05),且不影响细胞活力,而地塞米松抑制NO生成。胰岛素与二氨基嘧啶酮和蝶酰三谷氨酸共同作用时,抑制胰岛素诱导的NO生成。抗坏血酸独立于胰岛素增加NO生成,甲氨蝶呤不影响胰岛素对NO生成的作用。
胰岛素通过BH(4)合成的从头合成途径增加TM细胞中的NO生成。胰岛素可能通过增强TM细胞中的NO生成参与小梁网房水流出的调节。