Dourado Lays Fernanda Nunes, da Silva Flavia Rodrigues, Toledo Cibele Rodrigues, da Silva Carolina Nunes, Santana Cleildo Pereira, da Costa Bruna Lopes, de Lima Maria Elena, Cunha Armando da Silva
School of Pharmacy, Federal University of Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.
National Institute of Science and Technology in Pharmaceutical Nanotechnology, São Paulo, SP, Brazil.
J Venom Anim Toxins Incl Trop Dis. 2020 Sep 23;26:e20200031. doi: 10.1590/1678-9199-JVATITD-2020-0031. eCollection 2020.
PnPa11 and PnPa13 are synthetic peptides derived from 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.
The cytotoxicity and the antiangiogenic activity of these peptides were evaluated by the sulforhodamine-B method and chicken chorioallantoic membrane (CAM) assay, respectively. The 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.
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.
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.
PnPa11和PnPa13是源自蜘蛛毒液的合成肽,具有抗伤害感受和神经保护特性。在本研究中,我们评估了这些肽玻璃体内使用的安全性及其神经保护作用。
分别采用磺酰罗丹明-B法和鸡胚绒毛尿囊膜(CAM)试验评估这些肽的细胞毒性和抗血管生成活性。在Wistar大鼠右眼玻璃体内注射不同剂量(0.50;1.25;2.50;3.75和5.00μg/mL)的这些肽(n = 6),分析其安全性。通过视网膜电图检查(ERG)、眼压(IOP)和组织学分析评估视网膜功能。为了研究神经保护作用,Wistar大鼠右眼玻璃体内注射1.25μg/mL的肽(n = 6),然后暴露于蓝色LED光下。此外,还对视觉功能和视网膜微观结构进行了验证。
细胞毒性分析表明,这些肽对ARPE-19(成人视网膜色素上皮)细胞系无任何毒性,抗血管生成研究表明这些肽可促进血管减少。玻璃体内注射未引起重大变化,也未造成任何不可逆损害。在视网膜变性试验中,ERG记录表明,预先用PnPa11和PnPa13处理可保护视网膜免受损伤。形态学分析证实了ERG结果。免疫印迹分析显示,在光应激模型后,PnPa11增加了视网膜中Erk1/2、NR2A和NR2B的表达,但未引起Akt1激活,而PnPa13可防止Erk1/2和Akt1去磷酸化。
这些肽的眼内给药耐受性良好,并对视网膜变性具有保护活性,表明这些肽在眼科领域作为神经保护剂具有潜在用途。