间充质基质细胞衍生的分泌物对中腹蛛毒诱发家兔皮肌坏死的保护作用

IF 1.8 3区 医学 Q4 TOXICOLOGY
Gabriela Marques Rodrigues, Mara Elvira de Almeida, Sóstenes Apolo Correia Marcelino, Paula Bretas Ullmann Fernandes, Jessica Oliveira Pereira da Cruz, Françoise Louanne Araújo, Raquel da Silva Ferreira, Ana Flávia Machado Botelho, Francisco Javier Bedoya, Gladys Margot Cahuana, Ana Belén Hitos, Bernat Soria, Fernanda Costal-Oliveira, Clara Guerra Duarte, Juan R Tejedo, Carlos Chávez-Olórtegui, Marília Martins Melo
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引用次数: 0

摘要

背景:蛛网膜溃疡是指被蛛网膜溃疡属蜘蛛咬伤后引起的一系列临床表现。典型的临床症状是咬伤部位出现强烈的炎症反应,随后局部坏死,可归类为皮肤蛛网膜炎。这种皮肤型罗塞斯病很难治愈,所建议的治疗方法既不特异也不有效。本研究旨在评估间充质基质细胞衍生的分泌物对中腹蛛毒诱导的兔子皮损的保护作用:16只兔子分为4组(n = 4)。除第 1 组(G1)仅接受 PBS 外,其余三组(G2、G3 和 G4)均在肩胛间区域皮内注射 10 μg 中腹蛛毒液(稀释在 100 μL 0.9% 氯化钠中)。挑战 30 分钟后,除第 2 组外,其他各组都接受了分泌物处理。第 1 组(G1-对照组)皮内注射(ID)60 μg 的分泌物,溶于 0.15 M PBS;第 2 组(G2)通过皮内注射接受 0.9% NaCl;第 3 组(G3)通过皮内注射接受 60 μg 的分泌物;第 4 组(G4)通过静脉注射接受 60 μg 的分泌物。每天对兔子进行评估,15 天后对兔子实施安乐死,并对坏死病灶周围的皮肤样本进行尸体解剖和组织学分析:结果:G1 的兔子没有出现水肿、红斑、出血晕或坏死。G2、G3 和 G4 的兔子在 6 小时后出现水肿。然而,在 G2 和 G3 中观察到轻微水肿。G2、G3 和 G4 的动物在 6 小时和 3 天后出现出血晕。从宏观上看,在 G4 中,四只动物中只有一只的皮损演变成了脱皮伤口。显微镜下观察,G1 动物的皮肤没有发生任何变化。所有接触过中间蝇毒液的动物都出现了类似的变化,如坏死和异性浸润。然而,G4 的动物表现出成纤维细胞活化、结缔组织早期发育、新生血管形成和组织再上皮化,表明愈合过程更为显著:这些结果表明,在不含异种和人体成分的培养基中培养的间充质基质细胞分泌物组有望治疗罗氏蛛咬伤后引起的皮肤坏死。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective effects of mesenchymal stromal cell-derived secretome on dermonecrosis induced in rabbits by Loxosceles intermedia spider venom.

Background: Loxoscelism refers to a set of clinical manifestations caused by the bite of spiders from the Loxosceles genus. The classic clinical symptoms are characterized by an intense inflammatory reaction at the bite site followed by local necrosis and can be classified as cutaneous loxoscelism. This cutaneous form presents difficult healing, and the proposed treatments are not specific or effective. This study aimed to evaluate the protective effect of mesenchymal stromal cells-derived secretome on dermonecrosis induced by Loxosceles intermedia spider venom in rabbits.

Methods: Sixteen rabbits were distributed into four groups (n = 4). Except for group 1 (G1), which received only PBS, the other three groups (G2, G3, and G4) were initially challenged with 10 μg of L. intermedia venom, diluted in 100 μL of NaCl 0.9%, by intradermic injection in the interscapular region. Thirty minutes after the challenge all groups were treated with secretome, except for group 2. Group 1 (G1-control group) received intradermal injection (ID) of 60 μg of secretome in 0.15 M PBS; Group 2 (G2) received 0.9% NaCl via ID; Group 3 (G3) received 60 μg of secretome, via ID and Group 4 (G4), received 60 μg of secretome by intravenous route. Rabbits were evaluated daily and after 15 days were euthanized, necropsied and skin samples around the necrotic lesions were collected for histological analysis.

Results: Rabbits of G1 did not present edema, erythema, hemorrhagic halo, or necrosis. In animals from G2, G3, and G4, edema appeared after 6h. However, minor edema was observed in the animals of G2 and G3. Hemorrhagic halo was observed in animals, six hours and three days after, on G2, G3, and G4. Macroscopically, in G4, only one animal out of four had a lesion that evolved into a dermonecrotic wound. No changes were observed in the skin of the animals of G1, by microscopic evaluation. All animals challenged with L. intermedia venom showed similar alterations, such as necrosis and heterophilic infiltration. However, animals from G4 showed fibroblast activation, early development of connective tissue, neovascularization, and tissue re-epithelialization, indicating a more prominent healing process.

Conclusion: These results suggest that secretome from mesenchymal stromal cells cultured in a xeno-free and human component-free culture media can be promising to treat dermonecrosis caused after Loxosceles spiders bite envenoming.

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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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