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澳大利亚太攀蛇(Oxyuranus scutellatus)粗毒及主要神经毒素太攀蛇毒素的肌毒性活性。

Myotoxic activity of the crude venom and the principal neurotoxin, taipoxin, of the Australian taipan, Oxyuranus scutellatus.

作者信息

Harris J B, Maltin C A

出版信息

Br J Pharmacol. 1982 May;76(1):61-75. doi: 10.1111/j.1476-5381.1982.tb09191.x.

Abstract

1 The crude venom of the Australian taipan. Oxyuranus scutellatus and its principal neurotoxin, taipoxin, were injected into the anterolateral aspect of one hind limb of the rat. 2 The effects of the venom and toxin on the morphology and physiology on the underlying soleus muscles were examined. 3 Both the crude venom and the toxin caused necrosis and degeneration of the muscle. Damage to the peripheral muscle fibres could be seen at the light microscopic level as early as 3 h after injection of the toxic compounds. 4 The necrotic response was accompanied by an infiltration of phagocytic cells and an extensive oedema. The wet weight of the damaged muscles was almost doubled by 6 h. 5 In individual muscle fibres, necrosis was associated with the disruption of the plasma membrane and the disorganization of the myofibrils. The basal lamina of the muscle fibres was left intact. 6 Denervated mammalian muscles and innervated avian muscles were also destroyed by tiapoxin, but immature avian muscle growing in tissue culture was resistant. 7 Of the 3 subunits of taipoxin, only the basic alpha-taipoxin was itself myotoxic. However, its potency was enhanced by the presence of the acid gamma subunit. The role of the neutral beta-subunit is unclear. 8 The period of necrosis and degeneration lasted for approximately 48 h, after which the muscle fibres began to regenerate. Regeneration took place within the surviving basal lamina, with the formation of myotubes by three days, and small, immature muscle fibres by five days. Regeneration was virtually complete by 21 days.

摘要
  1. 将澳大利亚太攀蛇(Oxyuranus scutellatus)的粗毒液及其主要神经毒素太攀蛇毒素注入大鼠一侧后肢的前外侧。

  2. 研究了毒液和毒素对其下方比目鱼肌形态和生理的影响。

  3. 粗毒液和毒素均导致肌肉坏死和变性。早在注射有毒化合物后3小时,在光学显微镜下就能看到外周肌纤维受损。

  4. 坏死反应伴有吞噬细胞浸润和广泛水肿。6小时后,受损肌肉的湿重几乎增加了一倍。

  5. 在单个肌纤维中,坏死与质膜破坏和肌原纤维紊乱有关。肌纤维的基膜保持完整。

  6. 去神经支配的哺乳动物肌肉和有神经支配的鸟类肌肉也被太攀蛇毒素破坏,但在组织培养中生长的未成熟鸟类肌肉具有抗性。

  7. 在太攀蛇毒素的3个亚基中,只有碱性α-太攀蛇毒素本身具有肌毒性。然而,酸性γ亚基的存在增强了它的效力。中性β亚基的作用尚不清楚。

  8. 坏死和变性期持续约48小时,之后肌纤维开始再生。再生在存活的基膜内进行,3天时形成肌管,5天时形成小的、未成熟的肌纤维。到21天时再生基本完成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12bb/2068749/1b0ce045a1fb/brjpharm00628-0062-a.jpg

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