玻璃体内注射多肽PnPa11和PnPa13(黑栉蛛蛛毒液的衍生物)可防止视网膜损伤。

IF 1.8 3区 医学 Q4 TOXICOLOGY
Lays Fernanda Nunes Dourado, Flavia Rodrigues da Silva, Cibele Rodrigues Toledo, Carolina Nunes da Silva, Cleildo Pereira Santana, Bruna Lopes da Costa, Maria Elena de Lima, Armando da Silva Cunha
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引用次数: 1

摘要

背景:PnPa11和PnPa13是从黑栉蛛毒液中提取的合成肽,具有抗伤害和神经保护作用。在这项工作中,我们评估了玻璃体内使用的安全性和这些肽的神经保护作用。方法:分别采用磺胺硫丹- b法和鸡绒毛膜尿囊膜(CAM)法测定其细胞毒性和抗血管生成活性。在Wistar大鼠体内注射不同剂量(0.50;1.25;2.50;3.75和5.00µg/mL)的肽(右眼,n = 6)。通过视网膜电图检查(ERG)、眼内压(IOP)和组织学分析评估视网膜功能。为了研究其神经保护作用,我们在右眼玻璃体内注射1.25µg/mL多肽,然后用蓝色LED光照射Wistar大鼠。此外,还验证了视觉功能和视网膜微观结构。结果:细胞毒性分析表明,肽对ARPE-19(成人视网膜色素上皮)细胞系没有任何毒性,抗血管生成研究强调,肽促进血管的减少。玻璃体内注射没有引起大的改变,也没有引起任何不可逆的损伤。在视网膜变性试验中,ERG记录显示,先前使用PnPa11和PnPa13治疗可以保护视网膜免受损伤。形态学分析证实了ERG的发现。免疫印迹分析显示,PnPa11增加了光应激模型后Erk1/2、NR2A和NR2B的视网膜表达,但不引起Akt1激活,而PnPa13阻止Erk1/2和Akt1去磷酸化。结论:眼内给药这些多肽耐受性良好,对视网膜变性具有保护作用,提示这些多肽在眼科领域作为神经保护剂的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intravitreal injection of peptides PnPa11 and PnPa13, derivatives of <i>Phoneutria nigriventer</i> spider venom, prevents retinal damage.

Intravitreal injection of peptides PnPa11 and PnPa13, derivatives of <i>Phoneutria nigriventer</i> spider venom, prevents retinal damage.

Intravitreal injection of peptides PnPa11 and PnPa13, derivatives of <i>Phoneutria nigriventer</i> spider venom, prevents retinal damage.

Intravitreal injection of peptides PnPa11 and PnPa13, derivatives of Phoneutria nigriventer spider venom, prevents retinal damage.

Background: PnPa11 and PnPa13 are synthetic peptides derived from Phoneutria nigriventer spider venom, which display antinociceptive and neuroprotective properties. In this work, we evaluated the safety of intravitreal use and the neuroprotective effect of these peptides.

Methods: The cytotoxicity and the antiangiogenic activity of these peptides were evaluated by the sulforhodamine-B method and chicken chorioallantoic membrane (CAM) assay, respectively. The in vivo safety was analyzed in Wistar rats that were intravitreally injected with different doses (0.50; 1.25; 2.50; 3.75 and 5.00 µg/mL) of these peptides (right eye, n = 6). The retinal function was assessed by electroretinography exams (ERG), intraocular pressure (IOP), and histological analyzes. In order to investigate the neuroprotective effect, Wistar rats received intravitreal injections (right eye, n = 6) of peptides at 1.25 µg/mL and then were exposed to blue LED light. In addition, the visual function and the retinal microstructure were verified.

Results: Cytotoxicity analyses demonstrated that the peptides did not present any toxicity over ARPE-19 (adult retinal pigmented epithelial) cell line and the antiangiogenic study highlighted that the peptides promoted the reduction of blood vessels. The intravitreal injection did not cause major changes, neither induced any irreversible damage. In the retinal degeneration assay, the ERG records demonstrated that the prior treatment with PnPa11 and PnPa13 protected the retina from damage. Morphological analyses confirmed the ERG findings. Immunoblotting analyses revealed that PnPa11 increased Erk1/2, NR2A, and NR2B retinal expression after the light stress model, but did not cause Akt1 activation, while PnPa13 prevented Erk1/2 and Akt1 dephosphorylation.

Conclusions: The intraocular administration of these peptides was well tolerated and presented protective activity against retinal degeneration, suggesting the potential use of these peptides as neuroprotectors in the ophthalmological field.

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来源期刊
CiteScore
4.80
自引率
8.30%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Journal of Venomous Animals and Toxins including Tropical Diseases (JVATiTD) is a non-commercial academic open access publication dedicated to research on all aspects of toxinology, venomous animals and tropical diseases. Its interdisciplinary content includes original scientific articles covering research on toxins derived from animals, plants and microorganisms. Topics of interest include, but are not limited to:systematics and morphology of venomous animals;physiology, biochemistry, pharmacology and immunology of toxins;epidemiology, clinical aspects and treatment of envenoming by different animals, plants and microorganisms;development and evaluation of antivenoms and toxin-derivative products;epidemiology, clinical aspects and treatment of tropical diseases (caused by virus, bacteria, algae, fungi and parasites) including the neglected tropical diseases (NTDs) defined by the World Health Organization.
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