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人类白内障形成过程中脂质过氧化分析及成熟阶段的电子显微镜观察:用于预防白内障的Can-C N-乙酰肉碱前药润滑眼药水的药代动力学测定。

Analysis of lipid peroxidation and electron microscopic survey of maturation stages during human cataractogenesis: pharmacokinetic assay of Can-C N-acetylcarnosine prodrug lubricant eye drops for cataract prevention.

作者信息

Babizhayev Mark A

机构信息

Innovative Vision Products Inc., County of New Castle, Delaware 19810, USA.

出版信息

Drugs R D. 2005;6(6):345-69. doi: 10.2165/00126839-200506060-00004.

Abstract

Morphological and biophysical techniques described in this study have shown that membrane derangement occurs in human cataractous lenses. The data suggest that these disruptions were globules, vacuoles, multilamellar membranes and clusters of highly undulating membranes. Deleterious structural damage of the lens fibre cell plasma membranes serve as the primary light-scattering centres that cause the observed lens opacity. Nuclear cataract, a major cause of loss of lens transparency in the aging human, has been thought to be associated with oxidative damage, particularly at the site of the nuclear plasma membrane. Phospholipid molecules modified by oxygen accumulate in the lipid bilayer, change its geometry and impair lipid-lipid and protein-lipid interactions in lenticular fibre membranes. Lipid peroxidation (LPO) is a causative and pathogenic factor in cataract. Increased concentrations of primary molecular LPO products (diene conjugates, lipid hydroperoxides, oxy-derivatives of phospholipid fatty acids) and end-fluorescent LPO products have been detected in the lipid moieties of aqueous humour samples and human lenses obtained from patients with senile and complicated cataracts as compared with normal donors. In the present study, a rapid and simple high-performance liquid chromatographic (HPLC) assay for determination of imidazole-containing dipeptides in the aqueous humour of the eye was developed. The method was applied to determine the pharmacokinetic parameters and the time-course of N-acetylcarnosine and L-carnosine-related product in the eye, following a single dosage of topical ocular administration of peptide. Utilising data from pharmacokinetic studies and the specific purity of the N-acetylcarnosine (NAC) ingredient as a source of the pharmacological principle L-carnosine, we have created an ophthalmic time-release prodrug form including the US FDA-approved carboxymethylcellulose lubricant and other essential ingredients (Can-C, private label Nu-Eyes). This formulation increases the intraocular absorption of L-carnosine in the aqueous humour and optimises its specific antioxidant activity in vivo while reducing the toxic effects of lipid peroxides on the crystalline lens. L-carnosine that enters the aqueous humour can accumulate in the lens tissue for a reasonable period of time. The presence of L-carnosine in transparent crystalline lenses during normal aging was detected and its concentration in this case was about 25 microM. At different stages of cataract development, the level of L-carnosine drastically decreased, reaching about 5 microM in ripe human cataracts. However, administration of pure L-carnosine (1% solution) to the rabbit eye (instillation or subconjunctival injection) does not lead to accumulation of this natural compound in the aqueous humour at the time level over 30 minutes at a concentration exceeding that in placebo-treated matched eyes, and its effective concentration is exhausted more rapidly. Use of NAC prodrug eye drops optimises the clinical effects of L-carnosine in the treatment of ophthalmic disorders (such as prevention and reversal of cataracts in human and animal [canine] eyes). The data provided predict a clinical effect with NAC ophthalmic prodrug, and show that the magnitude and duration of this effect are directly related to the bioavailability of L-carnosine released from NAC in the aqueous humour of the anterior eye segment. The ophthalmic NAC drug shows promise in the treatment of a range of ophthalmic disorders that have a component of oxidative stress in their pathogenesis (including cataract, glaucoma, dry eye, vitreous floaters, inflammatory disorders, and corneal, retinal and systemic diseases [such as diabetes mellitus and its ophthalmic complications]). There is a need for further and better collaboration between Innovative Vision Products' cataract control and ophthalmic services, improved education of people affected by cataract, a commitment that N-acetylcarnosine eye drops will be the preferred treatment before orthodox cataract surgery is attempted, and consideration of outcomes and a possible role of the NAC drug cataract treatment as source of referral for orthodox surgical, ophthalmic and optometric services.

摘要

本研究中描述的形态学和生物物理技术表明,人类白内障晶状体中会发生膜紊乱。数据表明,这些破坏表现为小球、液泡、多层膜和高度起伏的膜簇。晶状体纤维细胞质膜的有害结构损伤是导致观察到的晶状体混浊的主要光散射中心。核性白内障是老年人晶状体透明度丧失的主要原因,一直被认为与氧化损伤有关,尤其是在核质膜部位。被氧修饰的磷脂分子在脂质双分子层中积累,改变其几何形状,并损害晶状体纤维膜中的脂质-脂质和蛋白质-脂质相互作用。脂质过氧化(LPO)是白内障的一个致病和发病因素。与正常供体相比,在老年性和复杂性白内障患者的房水样本和人晶状体的脂质部分中,已检测到初级分子LPO产物(二烯共轭物、脂质氢过氧化物、磷脂脂肪酸的氧衍生物)和终末荧光LPO产物的浓度增加。在本研究中,开发了一种快速简便的高效液相色谱(HPLC)法,用于测定眼房水中含咪唑二肽的含量。该方法用于测定单次局部眼部给药肽后,眼内N-乙酰肌肽和L-肌肽相关产物的药代动力学参数和时间进程。利用药代动力学研究数据以及N-乙酰肌肽(NAC)成分作为药理原理L-肌肽来源的特定纯度,我们制备了一种眼用缓释前药制剂,其中包括美国食品药品监督管理局批准的羧甲基纤维素润滑剂和其他必需成分(Can-C,自有品牌Nu-Eyes)。这种制剂增加了L-肌肽在房水中的眼内吸收,并优化了其在体内的特定抗氧化活性,同时降低了脂质过氧化物对晶状体的毒性作用。进入房水的L-肌肽可以在晶状体组织中积累一段合理的时间。在正常衰老过程中,透明晶状体中检测到L-肌肽的存在,此时其浓度约为25微摩尔。在白内障发展的不同阶段,L-肌肽水平急剧下降,在成熟的人类白内障中降至约5微摩尔。然而,将纯L-肌肽(1%溶液)滴入兔眼(滴眼或结膜下注射),在超过30分钟的时间内,该天然化合物在房水中的浓度不会超过安慰剂处理的对照眼,且其有效浓度更快耗尽。使用NAC前药滴眼液可优化L-肌肽在治疗眼部疾病(如预防和逆转人类和动物[犬]眼中的白内障)中的临床效果。所提供的数据预测了NAC眼用前药的临床效果,并表明该效果的大小和持续时间与从NAC释放到眼前节房水中的L-肌肽的生物利用度直接相关。眼用NAC药物在治疗一系列发病机制中存在氧化应激成分的眼部疾病(包括白内障、青光眼、干眼症、玻璃体混浊、炎症性疾病以及角膜、视网膜和全身性疾病[如糖尿病及其眼部并发症])方面显示出前景。创新视觉产品公司的白内障控制与眼科服务之间需要进一步加强更好的合作,改善对白内障患者的教育,承诺在尝试传统白内障手术之前,N-乙酰肌肽滴眼液将是首选治疗方法,并考虑NAC药物治疗白内障的结果及其作为传统手术、眼科和验光服务转诊来源的可能作用。

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