کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2572370 1561193 2014 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The renal effects and initial characterization of venom from Philodryas nattereri Steindachner, 1870
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
The renal effects and initial characterization of venom from Philodryas nattereri Steindachner, 1870
چکیده انگلیسی


• We investigated the effect of P. nattereri venom on the isolated perfused kidney.
• We study the mechanism of cytotoxicity of venom on renal epithelial cells.
• We demonstrated P. nattereri venom is composed for 86.3% of proteins.
• The venom of is capable of changing the kidney functional parameters.

The venom of the snake Philodryas nattereri is a mixture of proteins and toxic peptides with several important local and systemic actions, which are similar to those occurring in Bothrops snake bites. The mechanisms involved in the local and systemic actions of this venom are unknown. The aims of the work were to initial characterization of P. nattereri venom and investigate the effects of the poison in the renal perfusion system and in cultured renal tubular cells of the type MDCK (Madin–Darby canine kidney). The P. nattereri venom is composed majority of proteins (86.3%) and this poison promoted changes in all the evaluated renal parameters, mainly decreasing renal perfusion pressure (PP) and renal vascular resistance (RVR) and increasing urine flow (UF) and glomerular filtration rate (GFR). The most relevant result was that this venom was highly detrimental to the renal tubules independent of the PP reduction, which was shown by a decrease in sodium (Na+), potassium (K+) and chloride (Cl−) electrolyte transport in the studied concentrations. The glomeruli and tubules contain protein bodies and blood extravasation, which were observed by histological analysis. The venom of P. nattereri reduced viability of the MDCK cells only at high concentrations (50 and 100 μg/mL) with an IC50 of 169.5 μg/mL.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology Reports - Volume 1, 2014, Pages 812–819
نویسندگان
, , , , , , , , ,