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The Bite of the Honeybee: 2-Heptanone Secreted from Honeybee Mandibles during a Bite Acts as a Local Anaesthetic in Insects and Mammals

机译:蜜蜂叮咬:咬期间2-庚酮分泌从蜜蜂颌骨作为局部麻醉剂在昆虫和哺乳动物

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摘要

Honeybees secrete 2-heptanone (2-H) from their mandibular glands when they bite. Researchers have identified several possible functions: 2-H could act as an alarm pheromone to recruit guards and soldiers, it could act as a chemical marker, or it could have some other function. The actual role of 2-H in honeybee behaviour remains unresolved. In this study, we show that 2-H acts as an anaesthetic in small arthropods, such as wax moth larva (WML) and Varroa mites, which are paralysed after a honeybee bite. We demonstrated that honeybee mandibles can penetrate the cuticle of WML, introducing less than one nanolitre of 2-H into the WML open circulatory system and causing instantaneous anaesthetization that lasts for a few minutes. The first indication that 2-H acts as a local anaesthetic was that its effect on larval response, inhibition and recovery is very similar to that of lidocaine. We compared the inhibitory effects of 2-H and lidocaine on voltage-gated sodium channels. Although both compounds blocked the hNav1.6 and hNav1.2 channels, lidocaine was slightly more effective, 2.82 times, on hNav.6. In contrast, when the two compounds were tested using an ex vivo preparation–the isolated rat sciatic nerve–the function of the two compounds was so similar that we were able to definitively classify 2-H as a local anaesthetic. Using the same method, we showed that 2-H has the fastest inhibitory effect of all alkyl-ketones tested, including the isomers 3- and 4-heptanone. This suggests that natural selection may have favoured 2-H over other, similar compounds because of the associated fitness advantages it confers. Our results reveal a previously unknown role of 2-H in honeybee defensive behaviour and due to its minor neurotoxicity show potential for developing a new local anaesthetic from a natural product, which could be used in human and veterinary medicine.
机译:蜜蜂叮咬时会从下颌腺分泌2-庚酮(2-H)。研究人员已经确定了几种可能的功能:2-H可以充当警报信息素来招募警卫和士兵,它可以充当化学标记,或者还可以具有其他功能。 2-H在蜜蜂行为中的实际作用仍未解决。在这项研究中,我们表明2-H在小型节肢动物中扮演麻醉剂的角色,例如在蜜蜂叮咬后瘫痪的蜡蛾幼虫(WML)和Varroa螨。我们证明了蜜蜂的下颌骨可以穿透WML的表皮,将少于一纳升的2-H引入WML开放循环系统,并引起持续几分钟的瞬时麻醉。 2-H作为局麻药的第一个迹象是它对幼虫反应,抑制和恢复的作用与利多卡因非常相似。我们比较了2-H和利多卡因对电压门控钠通道的抑制作用。尽管这两种化合物均阻断了hNav1.6和hNav1.2通道,但利多卡因对hNav.6的疗效略高,为2.82倍。相反,当使用离体制剂(离体大鼠坐骨神经)测试这两种化合物时,这两种化合物的功能是如此相似,以至于我们可以将2-H明确地分类为局部麻醉剂。使用相同的方法,我们表明2-H具有所有测试的烷基酮,包括异构体3-和4-庚酮,具有最快的抑制作用。这表明自然选择可能比其他类似化合物更喜欢2-H,因为它具有相关的适应性优势。我们的研究结果揭示了2-H在蜜蜂防御行为中的未知作用,并且由于其较小的神经毒性,因此显示了从天然产物开发出新的局部麻醉剂的潜力,该麻醉剂可用于人类和兽医学。

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