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      Comparative compositional and functional venomic profiles among venom specimens from juvenile, subadult and adult Russell’s viper ( Daboia siamensis ): correlation with renal pathophysiology in experimental rabbits

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          Abstract

          Background:

          Eastern Russell’s viper ( Daboia siamensis) is one of the most medically significant snakes responsible for the development of acute renal failure. However, variation of the clinical picture and renal pathophysiology following bites by young and adult D. siamensis have not been elucidated.

          Methods:

          In this study, we analyzed the venomic profiles of D. siamensis at different maturation stages of juvenile, subadult and adult groups. The same pooled venom from each group was subjected to enzymatic, electrophoretic and proteomic analysis, including sublethal toxicity (0.1 mg/kg iv.) examined on bodily functions by comparing the venom compositional and functional profiles among venom specimens from juvenile, subadult and adult D. siamensis by correlating them with the renal pathophysiology in experimental rabbits.

          Results:

          The comparative studies revealed that juvenile venom possessed higher phospholipase A 2, metalloproteinase and serine proteinase levels, while subadult and adult venoms contained more L-amino acid oxidase, phosphodiesterase, the Kunitz-type serine protease inhibitor, disintegrin families and endothelial growth factor. An in vivo study revealed that the adult and subadult venoms caused persistent hypotension and bradycardia, while thrombocytopenia was a more characteristic effect of juvenile venom. All venom age groups showed significant reductions in renal hemodynamics and electrolyte excretions. The juvenile venom caused a higher tubulonephrosis lesion score than adult and subadult venoms.

          Conclusions:

          The D. siamensis venom shows an ontogenetic shift in its compositions and activities. Renal function alterations after envenomation depend on either the synergistic actions of different venom components or the disproportionate expression between the concentrations of enzymatic and non-enzymatic proteins in each age venom group. The high proportion of enzymatic toxin proteins in the juvenile venom results in greater nephrotoxicity.

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            Mechanisms and regulation of endothelial VEGF receptor signalling.

            Vascular endothelial growth factors (VEGFs) and their receptors (VEGFRs) are uniquely required to balance the formation of new blood vessels with the maintenance and remodelling of existing ones, during development and in adult tissues. Recent advances have greatly expanded our understanding of the tight and multi-level regulation of VEGFR2 signalling, which is the primary focus of this Review. Important insights have been gained into the regulatory roles of VEGFR-interacting proteins (such as neuropilins, proteoglycans, integrins and protein tyrosine phosphatases); the dynamics of VEGFR2 endocytosis, trafficking and signalling; and the crosstalk between VEGF-induced signalling and other endothelial signalling cascades. A clear understanding of this multifaceted signalling web is key to successful therapeutic suppression or stimulation of vascular growth.
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              Vascular endothelial growth factor: basic science and clinical progress.

              Vascular endothelial growth factor (VEGF) is an endothelial cell-specific mitogen in vitro and an angiogenic inducer in a variety of in vivo models. Hypoxia has been shown to be a major inducer of VEGF gene transcription. The tyrosine kinases Flt-1 (VEGFR-1) and Flk-1/KDR (VEGFR-2) are high-affinity VEGF receptors. The role of VEGF in developmental angiogenesis is emphasized by the finding that loss of a single VEGF allele results in defective vascularization and early embryonic lethality. VEGF is critical also for reproductive and bone angiogenesis. Substantial evidence also implicates VEGF as a mediator of pathological angiogenesis. In situ hybridization studies demonstrate expression of VEGF mRNA in the majority of human tumors. Anti-VEGF monoclonal antibodies and other VEGF inhibitors block the growth of several tumor cell lines in nude mice. Clinical trials with various VEGF inhibitors in a variety of malignancies are ongoing. Very recently, an anti-VEGF monoclonal antibody (bevacizumab; Avastin) has been approved by the Food and Drug Administration as a first-line treatment for metastatic colorectal cancer in combination with chemotherapy. Furthermore, VEGF is implicated in intraocular neovascularization associated with diabetic retinopathy and age-related macular degeneration.
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                Author and article information

                Journal
                J Venom Anim Toxins Incl Trop Dis
                J Venom Anim Toxins Incl Trop Dis
                jvatitd
                The Journal of Venomous Animals and Toxins Including Tropical Diseases
                Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP)
                1678-9199
                04 April 2022
                2022
                : 28
                : 20210111
                Affiliations
                [1 ]Queen Saovabha Memorial Institute, The Thai Red Cross Society, Pathumwan, Bangkok, Thailand.
                [2 ]Center of Excellence for Companion Animal Cancer, Department of Veterinary Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.
                [3 ]Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University, Ratchathewi, Bangkok, Thailand.
                Author notes
                [* ] Correspondence: Narongsak.C@ 123456chula.ac.th

                Competing interests: All authors have no competing interests to disclose.

                Author Contributions: NC, LC, TV, PL, OK, AR and VS designed the study. NC, LC, TV and PL conducted data curation. NC, LC, TV, PL, OK, AR and VS carried out formal analysis. NC and VS were in charge of funding acquisition. NC, LC, TV, PL, OK, AR and OR carried out investigation. NC, OK and OR were responsible fot methodology. NC and VS administred the project. NC, LC, TV, PL, OK, AR and OR were responsible for the resources. NC, LC, TV, PL and OR conducted software analysis. NC, LC, TV, PL, OK, AR and OR validated the study. NC and LC carried out original draft writing. NC, LC, OK and OR reviewed and edited the manuscript. All authors read and approved the final manuscript.

                Author information
                http://orcid.org/0000-0002-3207-0885
                http://orcid.org/0000-0003-2425-5000
                http://orcid.org/0000-0001-8197-0356
                http://orcid.org/0000-0002-2963-4811
                http://orcid.org/0000-0002-0950-2045
                http://orcid.org/0000-0001-6137-969X
                http://orcid.org/0000-0002-1154-6485
                http://orcid.org/0000-0002-4885-0405
                Article
                00309
                10.1590/1678-9199-JVATITD-2021-0111
                8978910
                35432494
                125b9f36-198c-465a-87b5-258c992fdaae

                This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/ ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/ ) applies to the data made available in this article, unless otherwise stated.

                History
                : 21 October 2021
                : 15 December 2021
                Page count
                Figures: 10, Tables: 2, Equations: 0, References: 103
                Categories
                Research

                daboia siamensis,venomics,snake age,renal pathophysiology,rabbit

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