Georgadze A K, Permiakov N K, Penin V A, Titov M I, Titova G P
Farmakol Toksikol. 1986 Nov-Dec;49(6):66-70.
The experiments on 24 dogs with experimental hemorrhagic pancreonecrosis showed that contrykal and 5-fluorouracil insignificantly decrease the area of the damaged parenchyma, fail to cease progression of the pancreas destruction. The peptide drug dalargin in these conditions increased the antitryptic activity and normalized BAEE esterase activity. Dalargin abolished erythrostasis and microthromboses in the vessels of the microcirculation, restored the blood supply throughout the area of the exocrine parenchyma, limited necrotic foci and suspended the development of pancreonecrosis.
对24只患有实验性出血性胰腺坏死的狗进行的实验表明,抑肽酶和5-氟尿嘧啶对受损实质面积的减小作用不显著,无法阻止胰腺破坏的进展。在这些情况下,肽类药物达洛argin增加了抗胰蛋白酶活性并使BAEE酯酶活性恢复正常。达洛argin消除了微循环血管中的红细胞淤滞和微血栓形成,恢复了整个外分泌实质区域的血液供应,限制了坏死灶并中止了胰腺坏死的发展。