Department of Ophthalmology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Laboratory of Photobiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Sci Rep. 2023 Mar 7;13(1):3772. doi: 10.1038/s41598-023-30908-1.
Myopia is becoming more common across the world, necessitating the development of preventive methods. We investigated the activity of early growth response 1 (EGR-1) protein and discovered that Ginkgo biloba extracts (GBEs) activated EGR-1 in vitro. In vivo, C57BL/6 J mice were fed either normal or 0.0667% GBEs (200 mg/kg) mixed chow (n = 6 each), and myopia was induced with - 30 diopter (D) lenses from 3 to 6 weeks of age. Refraction and axial length were measured by an infrared photorefractor and an SD-OCT system, respectively. In lens-induced myopia mice, oral GBEs significantly improved refractive errors (- 9.92 ± 1.53 D vs. - 1.67 ± 3.51 D, p < 0.001) and axial elongation (0.22 ± 0.02 mm vs. 0.19 ± 0.02 mm, p < 0.05). To confirm the mechanism of GBEs in preventing myopia progression, the 3-week-old mice were divided into normally fed with either myopic-induced or non-myopic-induced groups and GBEs fed with either myopic-induced or non-myopic-induced groups (n = 10 each). Choroidal blood perfusion was measured with optical coherence tomography angiography (OCTA). In both non-myopic induced groups, compared to normal chow, oral GBEs significantly improved choroidal blood perfusion (8.48 ± 15.75%Area vs. 21.74 ± 10.54%Area, p < 0.05) and expression of Egr-1 and endothelial nitric oxide synthase (eNOS) in the choroid. In both myopic-induced groups, compared to normal chow, oral GBEs also improved choroidal blood perfusion (- 9.82 ± 9.47%Area vs. 2.29 ± 11.84%Area, p < 0.05) and was positively correlated with the change in choroidal thickness. These findings suggest that GBEs may inhibit the progression of myopia by improving choroidal blood perfusion.
近视在全球范围内越来越普遍,因此需要开发预防方法。我们研究了早期生长反应 1(EGR-1)蛋白的活性,发现银杏叶提取物(GBE)在体外激活了 EGR-1。在体内,将 C57BL/6J 小鼠分别用正常或 0.0667%GBE(200mg/kg)混合饲料喂养(每组 6 只),并在 3 至 6 周龄时用-30 屈光度(D)透镜诱导近视。分别通过红外视网膜折射仪和 SD-OCT 系统测量屈光度和眼轴长度。在透镜诱导的近视小鼠中,口服 GBE 可显著改善近视程度(-9.92±1.53D 与-1.67±3.51D,p<0.001)和眼轴伸长(0.22±0.02mm 与 0.19±0.02mm,p<0.05)。为了证实 GBE 预防近视进展的机制,将 3 周龄的小鼠分为正常喂养组、近视诱导组和非近视诱导组,以及 GBE 喂养组、近视诱导组和非近视诱导组(每组 10 只)。使用光学相干断层扫描血管造影术(OCTA)测量脉络膜血流灌注。在非近视诱导组中,与正常饲料相比,口服 GBE 可显著改善脉络膜血流灌注(8.48±15.75%Area 与 21.74±10.54%Area,p<0.05)和脉络膜 Egr-1 和内皮型一氧化氮合酶(eNOS)的表达。在近视诱导组中,与正常饲料相比,口服 GBE 也可改善脉络膜血流灌注(-9.82±9.47%Area 与 2.29±11.84%Area,p<0.05),且与脉络膜厚度的变化呈正相关。这些发现表明,GBE 可能通过改善脉络膜血流灌注来抑制近视的进展。