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dc.creatorSaravia Otten, Patricia
dc.creatorRobledo, Bárbara
dc.creatorEscalante Muñoz, Teresa
dc.creatorBonilla, Llira
dc.creatorRucavado Romero, Alexandra
dc.creatorLomonte, Bruno
dc.creatorHernández, Rosario
dc.creatorFlock, Jan-Ingmar
dc.creatorGutiérrez, José María
dc.creatorGastaldello, Stefano
dc.date.accessioned2017-06-09T16:19:17Z
dc.date.available2017-06-09T16:19:17Z
dc.date.issued2013-02
dc.identifier.citationhttp://onlinelibrary.wiley.com/doi/10.1002/mus.23489/abstract
dc.identifier.issn1097-4598
dc.identifier.urihttps://hdl.handle.net/10669/30080
dc.description.abstractIntroduction: Viperid snakebite envenomings are characterized by muscle necrosis and a deficient regenerative response. Methods: Homogenates from gastrocnemius muscles of mice injected with the venom of the snake Bothrops asper or with 2 tissue-damaging toxins were added to cultures of C2C12 myogenic cells. Myoblasts proliferation and fusion were assessed. Venom was detected by immunoassay in mouse muscle during the first week after injection. Results: Homogenates from venom-injected muscle induced a drop in the number of proliferating myoblasts and a complete elimination of myotube formation. The inhibitory effect induced by homogenates from venom-injected mice was abrogated by preincubation of the homogenate with antivenom antibodies but not with control antibodies. This finding provides evidence that the effect is due to the action of venom in the tissue. Conclusions: Our observations suggest that traces of venom in muscle tissue might inhibit myotube formation and preclude a successful regenerative response.es_ES
dc.language.isoen_USes_ES
dc.sourceMuscle & Nerve; Volumen 47, Número 2. 2013es_ES
dc.subjectAnimalses_ES
dc.subjectBothropses_ES
dc.subjectCell Differentiationes_ES
dc.subjectCrotalid Venomses_ES
dc.subjectMatrix Metalloproteinase 14es_ES
dc.subjectMicees_ES
dc.subjectMuscle, Skeletales_ES
dc.subjectMyoblastses_ES
dc.subjectNecrosises_ES
dc.titleHomogenates of skeletal muscle injected with snake venom inhibit myogenic differentiation in cell culturees_ES
dc.typeartículo original
dc.identifier.doi10.1002/mus.23489
dc.description.procedenceUCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias de la Salud::Instituto Clodomiro Picado (ICP)es_ES
dc.identifier.pmid23169301


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