Ziai M R, Russek S, Wang H C, Beer B, Blume A J
CNS Research Department, American Cyanamid Company, Pearl River, New York 10965.
J Pharm Pharmacol. 1990 Jul;42(7):457-61. doi: 10.1111/j.2042-7158.1990.tb06595.x.
This review discusses our present knowledge of the structure and activities of the mast cell degranulating peptide (MCDP). This peptide is a basic, 22 amino acid residue component of honey bee venom with striking immunological and pharmacological activities. MCDP is a potent anti-inflammatory agent, but at low concentrations it is a strong mediator of mast cell degranulation and histamine release. MCDP is also an epileptogenic neurotoxin, an avid blocker of the potassium channels and can cause a significant lowering of the blood pressure in rats. Some of the biological activities of MCDP appear to have distinct mechanisms and may represent a good illustration of the structure-function relationship.
本综述讨论了我们目前对肥大细胞脱颗粒肽(MCDP)的结构和活性的了解。这种肽是蜂毒的一种碱性22个氨基酸残基成分,具有显著的免疫和药理活性。MCDP是一种有效的抗炎剂,但在低浓度时,它是肥大细胞脱颗粒和组胺释放的强介质。MCDP也是一种致癫痫神经毒素,是钾通道的强力阻滞剂,可导致大鼠血压显著降低。MCDP的一些生物学活性似乎具有不同的机制,可能很好地说明了结构与功能的关系。