Komada F, Okumura K, Hori R
J Pharmacobiodyn. 1985 Jan;8(1):33-40. doi: 10.1248/bpb1978.8.33.
We compared the in vitro degradation of porcine and human insulin in the subcutaneous tissue of rat. The insulin degrading activity was largely confined to the 160000 X g supernatant fraction of subcutaneous tissue. The degradation of human insulin was approximately half that of porcine insulin in the supernatant fraction. The degradation of porcine insulin in subcutaneous tissue was inhibited by bacitracin, leupeptin, phosphoramidon, and Z-Gly-Pro-Leu-Gly, though the human insulin degradation was not. The degradation of both insulins was accelerated by glutathione. While the proteolytic enzyme activities of cathepsin-B and collagenase-like peptidase were detectable in subcutaneous tissue, chymotrypsin, elastase, kallikrein, alpha-thrombin, and trypsin activities were almost negligible. These in vitro studies suggest that human insulin is comparatively stable against proteolytic enzymes, probably collagenase-like peptidase or cathepsin-B, in the subcutaneous tissue, which support the in vivo evidence.
我们比较了猪胰岛素和人胰岛素在大鼠皮下组织中的体外降解情况。胰岛素降解活性主要局限于皮下组织160000×g超速离心后的上清组分中。在上清组分中,人胰岛素的降解速度约为猪胰岛素的一半。杆菌肽、亮抑酶肽、磷酰胺素和Z - 甘氨酰 - 脯氨酰 - 亮氨酰 - 甘氨酸可抑制皮下组织中猪胰岛素的降解,但对人胰岛素降解无抑制作用。谷胱甘肽可加速两种胰岛素的降解。虽然在皮下组织中可检测到组织蛋白酶B和类胶原酶肽酶的蛋白水解酶活性,但糜蛋白酶、弹性蛋白酶、激肽释放酶、α - 凝血酶和胰蛋白酶的活性几乎可忽略不计。这些体外研究表明,人胰岛素在皮下组织中对蛋白水解酶(可能是类胶原酶肽酶或组织蛋白酶B)具有相对稳定性,这支持了体内实验证据。