Pharmacokinetics of HLDF-6-AA Peptide in the Organism of Experimental Animals
- Autores: Zolotarev Y.1, Dadayan A.1, Kozik V.1, Shram S.1, Azev V.2, Bogachouk A.3, Lipkin V.3, Myasoedov N.1
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Afiliações:
- Institute of Molecular Genetics, Russian Academy of Sciences
- Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry, Pushchino Branch, Russian Academy of Sciences
- Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences
- Edição: Volume 45, Nº 6 (2019)
- Páginas: 514-521
- Seção: Article
- URL: https://journals.rcsi.science/1068-1620/article/view/229243
- DOI: https://doi.org/10.1134/S1068162019050145
- ID: 229243
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Resumo
Pharmacokinetics of the promising antitumor peptide HLDF-6-AA (Ac-ThrGlyGluAsnHisArg-NH2) was studied using its uniformly tritiated derivative. Experiments were performed on male Wistar rats, Balb/c mice and Chinchilla rabbits. The tritium labeled peptide [3H]HLDF-6-AA with the molar radioactivity of 50 Ci/mmol was obtained by the reaction of high-temperature solid-state catalytic isotope exchange (HSCIE). Under intravenous bolus administration of HLDF-6-AA peptide to rats and rabbits, the characteristics of its pharmacokinetic profile in the blood were obtained and the values of the main pharmacokinetic parameters of HLDF-6-AA peptide, and its active metabolite HisArg-NH2 were calculated. It was shown that parameters of the retention time in the body and the rate of elimination for peptides HLDF-6-AA and HisArg-NH2 in rats and rabbits are close and in rats they are about 7 and 21 min, respectively. It was shown that repeated administration of the drug does not lead to a change in its regular cumulation and does not cause a change in its pharmacokinetics compared with a single administration. The linearity of the dependence of pharmacokinetic parameters on the amount of administered peptide in the range of 2–22 mg/kg was proved in experiments in rats. As a result of the study of the distribution of HLDF-6-AA peptide and its metabolite HisArg-NH2 between the blood and peripheral tissues of mice, it was shown that the maximum concentration of HLDF-6-AA peptide is observed in the kidney tissues and a somewhat smaller concentration in the omentum. It was found that 15–20 min after intraperitoneal administration of HLDF-6-AA to mice, the concentration of HisArg-NH2 peptide begins to exceed the concentration of HLDF-6-AA peptide, which is caused by its greater resistance to proteolytic hydrolysis. The highest concentration of HisArg-NH2 peptide is observed in the kidney and liver tissues.
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Sobre autores
Yu. Zolotarev
Institute of Molecular Genetics, Russian Academy of Sciences
Autor responsável pela correspondência
Email: zolya@img.ras.ru
Rússia, Moscow, 123182
A. Dadayan
Institute of Molecular Genetics, Russian Academy of Sciences
Email: zolya@img.ras.ru
Rússia, Moscow, 123182
V. Kozik
Institute of Molecular Genetics, Russian Academy of Sciences
Email: zolya@img.ras.ru
Rússia, Moscow, 123182
S. Shram
Institute of Molecular Genetics, Russian Academy of Sciences
Email: zolya@img.ras.ru
Rússia, Moscow, 123182
V. Azev
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry, Pushchino Branch, Russian Academy of Sciences
Email: zolya@img.ras.ru
Rússia, Pushchino, Moscow oblast, 142290
A. Bogachouk
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences
Email: zolya@img.ras.ru
Rússia, Moscow, 117997
V. Lipkin
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences
Email: zolya@img.ras.ru
Rússia, Moscow, 117997
N. Myasoedov
Institute of Molecular Genetics, Russian Academy of Sciences
Email: zolya@img.ras.ru
Rússia, Moscow, 123182