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Título : | A mouse model to study the alterations in haemostatic and inflammatory parameters induced by Lonomia achelous caterpillar haemolymph |
Autor : | Barrios, M. Taylor, P Rodríguez-Acosta, Alexis Sánchez, E.E. Arocha-Piñango, Carmen L. Gil, A. Salazar, A.M. Carvajal, Z. Abad, M.J. Guerrero, B |
Palabras clave : | Haemostasis Inflammation Lonomia achelous TNF Nitric oxide Haemorrhagic syndrome |
Fecha de publicación : | 28-Nov-2013 |
Citación : | Toxicon;59: 547–554 (2012) |
Resumen : | A mouse model was established to reproduce the haemorrhagic syndrome which occurs in
humans after accidental contact with the hairs of the caterpillar Lonomia achelous (LA) and
measures the haemostatic and inflammatory alterations that occur as a result of this
contact. Mice were injected intradermally with different doses (0.4, 0.8 and 1.6 mg/animal)
of L. achelous haemolymph (LAH). Haematological (haemoglobin, haematocrit, platelet
count, differential leukocyte count), haemostatic (fibrinogen, plasminogen, factor XIII
[FXIII], fibrinolytic activity) and inflammatory parameters (tumour necrosis factor alpha
[TNF-a], nitric oxide [NO]) were measured at different times up to 48 h. C57BL/6 mice
responded to LAH injection, in terms of these parameters, in a manner similar to that seen
in humans, whereas the BALB/c mice were unresponsive. In C57BL/6 mice injected with
LAH, time course measurements showed: a) a reduction in the haemoglobin, haematocrit,
fibrinogen, FXIII and plasminogen levels, b) no effect on the platelet count and c) immediate
leukocytosis and an increase in the fibrinolytic activity in plasma. An inflammatory
response (TNF-a) was observed within 1 h post-injection, followed by a more persistent
increase in serum NO. These findings suggest that C57BL/6 mice represent a useful model
of the haemorrhagic syndrome observed in humans who have suffered contact with the
caterpillar, permitting a deeper understanding of the role of the inflammatory response in
the haematological and haemostatic manifestations of this syndrome. |
URI : | http://hdl.handle.net/10872/5124 |
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