Eysselein V E, Deveney C W, Sankaran H, Reeve J R, Walsh J H
Am J Physiol. 1983 Aug;245(2):G313-20. doi: 10.1152/ajpgi.1983.245.2.G313.
The biological activity of a recently characterized cholecystokinin molecule, canine CCK-58, has been tested using perifused canine gallbladder strips and isolated mouse pancreatic acini. It has been shown that canine CCK-58, purified by affinity chromatography and molecular sieve chromatography, is biologically as potent as canine CCK-39,33 (component II) and synthetic CCK-8. The biological responses were inhibited by dibutyryl cGMP, a known CCK antagonist. CCK-58 is one of the main large molecular forms of CCK in the intestine mucosa. Whether CCK-58 is only an intracellular precursor of other CCK molecules or an important circulating hormone cannot be determined from the data currently available.
最近鉴定出的一种胆囊收缩素分子——犬CCK - 58的生物活性,已通过灌注犬胆囊条和分离的小鼠胰腺腺泡进行了测试。结果表明,通过亲和层析和分子筛层析纯化的犬CCK - 58在生物学活性上与犬CCK - 39、33(组分II)和合成CCK - 8相当。已知的CCK拮抗剂二丁酰环鸟苷酸可抑制这些生物反应。CCK - 58是肠黏膜中CCK的主要大分子形式之一。根据目前可得的数据,尚无法确定CCK - 58仅仅是其他CCK分子的细胞内前体还是一种重要的循环激素。