Departamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Avenida do Café s/n, CEP 14040-903, Ribeirão Preto, SP, Brazil.
Toxicon. 2011 Jun;57(7-8):1101-8. doi: 10.1016/j.toxicon.2011.04.017. Epub 2011 Apr 29.
Scorpion envenomation induces a systemic immune response, and neurotoxins of venom act on specific ion channels, modulating neurotransmitter release or activity. However, little is known about the immunomodulatory effects of crude venom from scorpion Tityus serrulatus (TsV) or its toxins (Ts1, Ts2 and Ts6) in combination with lipopolysaccharide (LPS). To investigate the immunomodulatory effects of TsV and its toxins (Ts1, Ts2 and Ts6), J774.1 cells were stimulated with different concentrations (25, 50 and 100 μg/mL) of venom or toxins pre-stimulated or not with LPS (0.5 μg/mL). Macrophage cytotoxicity was assessed, and nitric oxide (NO) and cytokine production were analyzed utilizing the culture supernatants. TsV and its toxins did not produce cytotoxic effects. Depending on the concentrations used, TsV, Ts1 and Ts6 stimulated the production of NO, interleukin (IL)-6 and tumor necrosis factor (TNF)-α in J774.1 cells, which were enhanced under LPS co-stimulation. However, LPS + Ts2 inhibited NO, IL-6 and TNF-α production, and Ts2 alone stimulated the production of IL-10, suggesting an anti-inflammatory activity for this toxin. Our findings are important for the basic understanding of the mechanisms involved in macrophage activation following envenomation; additionally, these findings may contribute to the discovery of new therapeutic compounds to treat immune-mediated diseases.
蝎毒液会引起全身性免疫反应,毒液中的神经毒素会作用于特定的离子通道,调节神经递质的释放或活性。然而,目前对于粗制的 Tityus serrulatus(TsV)蝎毒液或其毒素(Ts1、Ts2 和 Ts6)与脂多糖(LPS)联合作用下的免疫调节作用知之甚少。为了研究 TsV 及其毒素(Ts1、Ts2 和 Ts6)的免疫调节作用,用不同浓度(25、50 和 100 μg/mL)的毒液或毒素(预先用或不用 LPS(0.5 μg/mL)预刺激)刺激 J774.1 细胞。通过检测巨噬细胞的细胞毒性,利用培养上清液分析一氧化氮(NO)和细胞因子的产生。TsV 和其毒素均未产生细胞毒性作用。TsV、Ts1 和 Ts6 依赖于所用浓度刺激 J774.1 细胞产生 NO、白细胞介素(IL)-6 和肿瘤坏死因子(TNF)-α,在 LPS 共刺激下,其产生量增加。然而,LPS+Ts2 抑制了 NO、IL-6 和 TNF-α的产生,而 Ts2 本身则刺激了 IL-10 的产生,表明该毒素具有抗炎活性。我们的研究结果对深入了解蝎毒引起的巨噬细胞激活的机制具有重要意义;此外,这些发现可能有助于发现治疗免疫介导性疾病的新治疗化合物。