UNESP, Avenida 24 A, 1515, CP 199, 13506-900 Rio Claro, SP, Brazil.
Toxicon. 2013 Sep;72:64-70. doi: 10.1016/j.toxicon.2013.06.007. Epub 2013 Jun 22.
Hymenoptera venoms are constituted by a complex mixture of chemically or pharmacologically bioactive agents, such as phospholipases, hyaluronidases and mastoparans. Venoms can also contain substances that are able to inhibit and/or diminish the genotoxic or mutagenic action of other compounds that are capable of promoting damages in the genetic material. Thus, the present study aimed to assess the effect of the venom of Polybia paulista, a neotropical wasp, by assays with HepG2 cells maintained in culture. The cytotoxic potential of the wasp venom, assessed by the methyl thiazolyl tetrazolium assay (MTT assay), was tested for the concentrations of 10 μg/mL, 5 μg/mL and 1 μg/mL. As these concentrations were not cytotoxic, they were used to evaluate the genotoxic (comet assay) and mutagenic potential (micronucleus test) of the venom. In this study, it was verified that these concentrations induced damages in the DNA of the exposed cells, and it was necessary to test lower concentrations until it was found those that were not considered genotoxic and mutagenic. The concentrations of 1 ng/mL, 100 pg/mL and 10 pg/mL, which did not induce genotoxicity and mutagenicity, were used in four different treatments (post-treatment, pre-treatment, simultaneous treatment with and without incubation), in order to evaluate if these concentrations were able to inhibit or decrease the genotoxic and mutagenic action of methyl methanesulfonate (MMS). None of the concentrations was able to inhibit and/or decrease the MMS activity. The genotoxic and mutagenic activity of the venom of P. paulista could be caused by the action of phospholipase, mastoparan and hyaluronidase, which are able to disrupt the cell membrane and thereby interact with the genetic material of the cells or even facilitate the entrance of other compounds of the venom that can act on the DNA. Another possible explanation for the genotoxicity and mutagenicity of the venom can be the presence of substances able to trigger inflammatory process and, consequently, generate oxygen reactive species that can interact with the DNA of the exposed cells.
膜翅目毒液由复杂的化学或药理学生物活性物质组成,如磷脂酶、透明质酸酶和蜂毒素。毒液还可能含有能够抑制和/或减少其他能够促进遗传物质损伤的化合物的遗传毒性或致突变作用的物质。因此,本研究旨在评估新热带黄蜂 Polybia paulista 的毒液通过培养的 HepG2 细胞检测的效果。通过噻唑蓝(MTT)测定法评估黄蜂毒液的细胞毒性潜力,测试浓度为 10μg/mL、5μg/mL 和 1μg/mL。由于这些浓度没有细胞毒性,因此用于评估毒液的遗传毒性(彗星试验)和致突变性(微核试验)。在这项研究中,已经验证了这些浓度会导致暴露细胞的 DNA 受损,并且必须测试更低的浓度,直到发现那些不被认为具有遗传毒性和致突变性的浓度。未诱导遗传毒性和致突变性的浓度 1ng/mL、100pg/mL 和 10pg/mL,用于四个不同的处理(后处理、预处理、同时处理和无孵育),以评估这些浓度是否能够抑制或降低甲基甲磺酸(MMS)的遗传毒性和致突变性。没有一个浓度能够抑制和/或降低 MMS 的活性。P. paulista 毒液的遗传毒性和致突变性可能是由磷脂酶、蜂毒素和透明质酸酶的作用引起的,这些酶能够破坏细胞膜,从而与细胞的遗传物质相互作用,甚至促进毒液中的其他化合物进入,这些化合物可以作用于 DNA。毒液的遗传毒性和致突变性的另一个可能解释是存在能够引发炎症过程的物质,从而产生能够与暴露细胞的 DNA 相互作用的活性氧物质。