The effect of platelet-rich plasma and sodium alginate hydrogel on corneal wound healing after corneal alkali burns in rats with computer-assisted anterior segment optical coherence tomography image analysis

IF 3 2区 医学 Q1 OPHTHALMOLOGY
Mehmet Omer Kiristioglu , Mehmet Baykara , Ozkan Yavas , Zehra Avci Kupeli , Musa Ozgur Ozyigit
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Abstract

Our objective was to determine the effect of a semi-synthetic sodium alginate hydrogel and its combination with platelet-rich plasma (PRP) on histopathological, biochemical, clinical, and anterior segment optical coherence tomography (AS-OCT) data. Alkali chemical burn of the cornea was induced. Injured rats were randomly divided into five equal groups and topically treated with phosphate-buffered saline (sham), platelet-rich plasma (PRP), 0.5% sodium citrate, a semi-synthetic sodium alginate hydrogel, or a combination of PRP and hydrogel (combined group) three times daily. The degree of corneal opacity (CO), corneal epithelial staining (CES), percentage of corneal epithelial defects (CEDP), degree of ciliary hyperemia (CH), neovascularization size (NVS), and extent of neovascularization (NVE) were evaluated. AS-OCT was performed at nine days, and then rats were sacrificed. Histological examination and enzyme-linked immunosorbent assays were performed to detect the concentrations of IL-1β and MMP-9 in the cornea. There were no significant differences between the groups regarding CEDP, CO, CES, CH, NVS, or NVE on the first day after corneal alkali burn injury (p > 0,05). At the last examination, CO was significantly lower in the PRP group than in the sham group (p = 0,044), while the CO concentrations were similar in terms of NVS (p > 0,05). Similarly, in terms of tissue MMP-9 levels, there were no significant differences between groups (p > 0,05). However, there was a significant difference in tissue IL-1β levels between the groups (p < 0,001). In the PRP and combined groups, the level of IL-1β was significantly lower than that in the sham group (p = 0,043 and p = 0,036, respectively). There was a significant difference in epithelial necrosis between the PRP, and it was the lowest in the combined group (p = 0,003). Epithelial thickness was highest in the combined group (p = 0,002). CEDP was significantly different at the last visit between the groups (p = 0.042). The fastest epithelial closing rate was observed for the combined group (p = 0,026). There was a significant negative correlation between tissue MMP-9 levels and corneal solidity and between tissue MMP-9 levels and the corneal area according to the AS-OCT measurements (p = 0,012 and p = 0,027, respectively). When used alone, topical hydrogel application did not significantly enhance the healing of corneal wounds. However, when combined with PRP, it leads to an increased rate of epithelial closure and neovascularization. This combination did not exacerbate inflammation or corneal opacity compared to PRP alone. The anticoagulant citrate solution in the PRP tube did not prove effective. The synergistic use of PRP and hydrogel could enhance epithelial thickness and reduce epithelial necrosis. The use of new parameters for corneal wound healing assessment was facilitated through AS-OCT image processing.

利用计算机辅助前段光学相干断层扫描图像分析富血小板血浆和海藻酸钠水凝胶对大鼠角膜碱烧伤后角膜伤口愈合的影响。
我们的目的是确定半合成海藻酸钠水凝胶及其与富血小板血浆(PRP)的结合对组织病理学、生化、临床和眼前节光学相干断层扫描(AS-OCT)数据的影响。诱导角膜碱化学烧伤。受伤大鼠被随机分为五个等量组,分别接受磷酸盐缓冲盐水(假组)、富血小板血浆(PRP)、0.5% 枸橼酸钠、半合成海藻酸钠水凝胶或 PRP 和水凝胶组合(组合组)的局部治疗,每天三次。对角膜混浊程度(CO)、角膜上皮染色(CES)、角膜上皮缺损百分比(CEDP)、睫状肌充血程度(CH)、新生血管大小(NVS)和新生血管范围(NVE)进行评估。九天后进行 AS-OCT,然后将大鼠处死。通过组织学检查和酶联免疫吸附试验检测角膜中 IL-1β 和 MMP-9 的浓度。在角膜碱烧伤后的第一天,各组间的 CEDP、CO、CES、CH、NVS 或 NVE 均无明显差异(P>0,05)。在最后一次检查时,PRP 组的 CO 明显低于假体组(p=0,044),而 NVS 的 CO 浓度相似(p>0,05)。同样,就组织 MMP-9 水平而言,各组之间没有显著差异(p>0,05)。然而,组织 IL-1β 水平在各组间存在显著差异(p
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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