| Grant number: | 16/23829-9 |
| Support Opportunities: | Scholarships abroad - Research Internship - Doctorate |
| Start date: | March 15, 2017 |
| End date: | March 14, 2018 |
| Field of knowledge: | Biological Sciences - Pharmacology |
| Principal Investigator: | Edson Antunes |
| Grantee: | Rita de Cássia de Oliveira Collaço |
| Supervisor: | Edward Gerard Rowan |
| Host Institution: | Faculdade de Ciências Médicas (FCM). Universidade Estadual de Campinas (UNICAMP). Campinas , SP, Brazil |
| Institution abroad: | University of Strathclyde, Scotland |
| Associated to the scholarship: | 16/11319-6 - The somatic and autonomic activities of Tityus bahiensis scorpion venom and its isolated fractions., BP.DR |
Abstract Scorpion envenomation produces local effects at the site of envenomation that can turn into systemic effects predominantly related to massive neurotransmitter release from central and peripheral nervous system. This neurotoxic activity has been attributed to neurotoxic peptides present in theses venoms that have great specificity and affinity for ion channels. Scorpion neurotoxins have been widely used as pharmacological tools to understand ion channel structure and its associated physiological role, as well as to evaluate their contribution to many ion channel related diseases (channelopathies) i.e. epilepsy, facial paralysis, muscular diseases, cardiac arrhythmia and pain syndromes, thus offering an unique insight into underlying cause of the disease and to aid the development of novel strategies for designing new classes of therapeutic drugs. Tityus bahiensis is the second most medically important scorpion specie in Brazil (the most important in the São Paulo State) and is widely distributed in the country with exception of the Northern Region of Brazil. Despite this, its venom and isolated fractions remain scarcely studied, especially with regarding to the peripheral (somatic and autonomic) nervous system and effects on ion channels on excitable tissues. Our preliminary data have shown that T. bahiensis venom is neurotoxic and its pharmacology is more likely due to effects on ion channels on somatic and autonomic nervous systems. This overseas placement's main aim is to improve the understanding of the pharmacology of the venom and associated peptide toxins using electrophysiological techniques i.e membrane potential recordings and patch-clamp recordings in addition to complementary calcium imaging techniques. The results of this research will help provide both physiological data on the pharmacology of the venom/ toxins and data on the isolation of peptides with pharmacological potential as both research tools and therapeutics. | |
| News published in Agência FAPESP Newsletter about the scholarship: | |
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