Kador Peter F, Guo Changmei, Kawada Hiroyoshi, Randazzo James, Blessing Karen
Department of Pharmaceutical Sciences, University of Nebraska Medical Center , Omaha, Nebraska.
J Ocul Pharmacol Ther. 2014 Sep;30(7):593-602. doi: 10.1089/jop.2014.0016.
Based on the hypothesis that oral nutraceuticals do not adequately reach all ocular tissues in the anterior segment, we evaluated the ability of a 3% concentration of the ingredients in a topical nutraceutical antioxidant formulation called Optixcare Eye Health (Optixcare EH) to ameliorate oxidative stress in rat models of age-related ocular diseases.
Diabetes was induced by tail-vein injection of streptozotocin, and the development of cataracts was monitored by slit lamp. Young rats were exposed to ultraviolet (UV) light, and the reduction in lens glutathione (GSH) levels and increase in 4-hydroxynonenol (4-HNE) were measured. Oxidative stress in the neural retina was generated by exposure of dark-adapted rats to 1,000 lx of light, and oxidative stress markers were measured. Dry eye was induced in rats by twice daily (b.i.d.) subcutaneous scopolamine injections. Topical Optixcare EH was administered b.i.d. and compared in select experiments to the multifunctional antioxidant JHX-4, the topical aldose reductase inhibitor (ARI) Kinostat™, oral Ocu-GLO™, and the topical ocular comfort agents Optixcare Eye Lube, Optixcare Eye Lube + Hyaluron, and Idrop Vet Plus hyaluronic acid.
In diabetic rats, topical ARI treatment prevented cataract formation while the nutraceuticals delayed their development with Optixcare EH>Ocu-GLO. In UV-exposed rats, the reduction of GSH and increase in 4-HNE in the lens were normalized in order JHX-4>Optixcare EH>Ocu-GLO. In the retina, oxidative stress markers were reduced better by oral JHX-4 compared with topical Optixcare EH. In the scopolamine-induced dry-eye rats, tear flow was maintained by Optixcare EH treatment, while none of the comfort agents examined altered tear flow.
Topical administration of a 3% concentration of the ingredients in Optixcare EH reduces experimentally induced reactive oxygen species in rats exposed to several sources of ocular oxidative stress. In addition, Optixcare EH maintains tear volume in scopolamine-induced dry eye. This suggests that in the anterior segment, the ingredients in Optixcare EH may have clinical potential against ocular oxidative stress.
基于口服营养保健品无法充分抵达眼前节所有眼组织这一假设,我们评估了一种名为Optixcare Eye Health(Optixcare EH)的局部营养保健品抗氧化剂配方中3%浓度成分改善年龄相关性眼部疾病大鼠模型氧化应激的能力。
通过尾静脉注射链脲佐菌素诱导糖尿病,并用裂隙灯监测白内障的发展。将幼鼠暴露于紫外线(UV)下,测量晶状体谷胱甘肽(GSH)水平的降低和4-羟基壬烯醛(4-HNE)的增加。通过将暗适应大鼠暴露于1000勒克斯的光照下在神经视网膜中产生氧化应激,并测量氧化应激标志物。通过每日两次(bid)皮下注射东莨菪碱在大鼠中诱导干眼。bid局部给予Optixcare EH,并在选定实验中与多功能抗氧化剂JHX-4、局部醛糖还原酶抑制剂(ARI)Kinostat™、口服Ocu-GLO™以及局部眼部舒适剂Optixcare Eye Lube、Optixcare Eye Lube + 透明质酸和Idrop Vet Plus透明质酸进行比较。
在糖尿病大鼠中,局部ARI治疗可预防白内障形成,而营养保健品可延缓其发展,Optixcare EH>Ocu-GLO。在UV暴露大鼠中,晶状体中GSH的降低和4-HNE的增加按JHX-4>Optixcare EH>Ocu-GLO的顺序恢复正常。在视网膜中,与局部Optixcare EH相比,口服JHX-4能更好地降低氧化应激标志物。在东莨菪碱诱导的干眼大鼠中,Optixcare EH治疗可维持泪液分泌,而所检测的舒适剂均未改变泪液分泌。
局部给予Optixcare EH中3%浓度的成分可降低暴露于多种眼部氧化应激源的大鼠实验性诱导的活性氧。此外,Optixcare EH可维持东莨菪碱诱导的干眼中的泪液量。这表明在眼前节,Optixcare EH中的成分可能具有对抗眼部氧化应激的临床潜力。