Department of Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Hirokoji-agaru, Kawaramachi-dori, Kamigyo-ku, Kyoto, 602-8566, Japan.
Oncolys BioPharma, Inc., Tokyo, 106-0032, Japan.
Sci Rep. 2020 Dec 1;10(1):20936. doi: 10.1038/s41598-020-77811-7.
Inhibition of fibrosis is indispensable for maintaining filtering blebs after glaucoma filtration surgery (GFS). The purpose of this study was to investigate the ability of a pluripotent epigenetic regulator OBP-801 (OBP) to ameliorate extracellular matrix formation in a rabbit model of GFS. Rabbits that underwent GFS were treated with OBP. The gene expression profiles and intraocular pressure (IOP) were monitored until 30 postoperative days. The bleb tissues were evaluated for tissue fibrosis at 30 postoperative days. In in vitro models, OBP interfered the functions of diverse genes during the wound-healing process. In in vivo GFS models, the expressions of TGF-β3, MMP-2, TIMP-2 and 3, LOX, COL1A and SERPINH1 were significantly inhibited at 30 postoperative days in the OBP group compared with those in the vehicle control group. OBP treatment involving subconjunctival injection or eye drops showed no adverse effects, and reduced levels of α-SMA and collagen deposition at the surgical wound site. OBP maintained the long-lived bleb without scar formation, and IOP was lower at 30 postoperative days compared with the vehicle control group. These findings suggest that OBP is an effective and useful candidate low-molecular-weight agent for improving wound healing and surgical outcomes in a rabbit model of GFS.
抑制纤维化对于维持青光眼滤过手术(GFS)后滤过泡的功能是必不可少的。本研究旨在探讨多能表观遗传调节剂 OBP-801(OBP)在兔 GFS 模型中改善细胞外基质形成的能力。接受 GFS 的兔子接受 OBP 治疗。监测基因表达谱和眼内压(IOP)至术后 30 天。术后 30 天评估滤过泡组织的纤维化程度。在体外模型中,OBP 在伤口愈合过程中干扰了多种基因的功能。在体内 GFS 模型中,与载体对照组相比,OBP 组在术后 30 天时 TGF-β3、MMP-2、TIMP-2 和 3、LOX、COL1A 和 SERPINH1 的表达明显受到抑制。结膜下注射或滴眼给予 OBP 治疗没有不良反应,并减少了手术部位 α-SMA 和胶原沉积的水平。OBP 维持了无瘢痕形成的长效滤过泡,术后 30 天的 IOP 低于载体对照组。这些发现表明,OBP 是一种有效的、有前途的低分子量药物候选物,可改善兔 GFS 模型中的伤口愈合和手术效果。