Inervación de la cabeza larga del músculo tríceps braquial / Innervation of the long head of triceps brachii muscle

Clásicamente, la inervación del músculo tríceps braquial se atribuye al nervio radial. Sin embargo, reportes clínicos han observado parálisis de la cabeza larga del músculo tríceps braquial posterior a lesiones del nervio axilar, ocurridas luego de una luxación de la articulación glenohumeral, poniendo en duda la inervación de la cabeza larga del músculo tríceps braquial. El objetivo del presente estudio es verificar la inervación de la cabeza larga del músculo tríceps braquial por parte del nervio axilar. Se disecaron 12 regiones posteriores de hombro y brazo, previamente fijadas en solución fijadora conservadora, identificando ramos de inervación del nervio axilar hacia la cabeza larga del músculo tríceps braquial, luego se obtuvieron muestras para estudio histológico con Hematoxilina-Eosina. Fue posible identificar en todos los casos ramos del nervio axilar, penetrando en la mitad superior de la cabeza larga del músculo tríceps braquial. El estudio histológico mostró una imagen compatible con tejido nervioso en todas las muestras analizadas. Estos resultados contrastan con las descripciones realizadas en textos clásicos respecto a la inervación del músculo tríceps braquial, el cual podría presentar una doble inervación proveniente de los nervios radial y axilar, o una inervación diferente para cada cabeza. Los hallazgos presentados aportan información a la hora de analizar las lesiones del nervio axilar post luxaciones de hombro, al realizar procedimientos quirúrgicos en esta región o en la planificación de la rehabilitación de estos pacientes.

Primarily, innervation of the triceps brachii muscle has been attributed to the axillary nerve. However, clinical reports have observed paralysis from the long head of the triceps brachii muscle following axillary nerve lesions which occurred after dislocation of the glenohumeral joint. This has raised questions about the innervation of the long head of triceps brachii muscle. The objective of this study was to verify the innervation of the long head of the triceps brachii muscle by the axillary nerve. Twelve previously fixed posterior areas of shoulder and arm were dissected and branches of innervation of the axillary nerve towards the long head of triceps brachii muscle were identified. Subsequently, samples were taken for histological hematoxylin-eosin study. In all cases, we observed branches of the axillary nerve penetrating the upper half of the long head of the triceps brachii muscle. The histological study showed an image compatible with nerve tissue in each sample analyzed. The results contrast with the description in classic texts regarding innervation of the triceps brachii muscle, which could present with double innervation from the radial and axillary nerves, or a separate innervation for each head. These results provide information for axillary nerve lesion analysis following shoulder dislocation, at the time of performing surgical procedures in the area, or when planning rehabilitation for these patients.

Angiogenic potential of the cerebrospinal fluid (CSF) of patients with high-grade gliomas measured with the chick embryo chorioallantoic membrane assay (CAM)

High-grade gliomas are highly vascularized tumors. Neo-angiogenesis plays a key role in tumor growth and resistance to therapy. A cerebrospinal fluid (CSF) sample could be a useful way to obtain pro-angiogenic predictive or prognostic markers at different stages of the disease. As a first step we looked for pro-angiogenic activity in the CSF of patients with high-grade gliomas. We performed the chicken embryo chorio-allantoic membrane (CAM) assay to study the angiogenic potential of the cerebrospinal fluid (CSF), obtained either by lumbar puncture (LP) or craniotomy from six patients with high-grade brain tumors (three glioblastoma (WHO grade IV), one anaplastic oligodendroglioma (WHO grade III), two anaplastic ganglioglioma (WHO grade III)), and four healthy controls. Significantly increased neo-angiogenesis was observed on the surface of the growing CAM in the 6 patients with high-grade gliomas compared to controls (3.69 ± 1.23 versus 2.16 ± 0.97 capillaries per area (mean ± SD), p<0.005). There was no statistical difference related to the hystological grade of the tumor (WHO grade III or IV), previous treatment (radio-chemotherapy plus temozolomide, temozolomide alone or no treatment), or the site of CSF sample (surgery or lumbar puncture). Our results suggest a pro-angiogenic potential in the CSF of patients with high-grade gliomas.

Betamethasone inhibits tumor development, microvessel density and prolongs survival in mice with a multiresistant adenocarcinoma TA3

Tumor resistance to traditional cancer treatments poses an important challenge to modern science. Thus, angiogenesis inhibition is an important emerging cancer treatment. Many drugs are tested and corticosteroids have shown interesting results. Herein we investigate the effect on microvessel density, survival time and tumoral volume of mice with TA3-MTX-R tumors. Twenty six mice were inoculated with lxlO6 tumor cells, 4-5 days after injection, six mice were injected with PBS (group A) and twenty mice were treated with p-met (group B). All animals from Group A died on day 22. Group B was divided into Bl (treated discontinued) and B2 (treated daily) and observed until day 88. All mice were processed for histo-immunohistochemical analysis and the blood vessels were counted. A decrease in microvessel density and tumoral volume and longer survival times were observed in the treated group. We propose that the antiangiogenic p-met effect explains, at least partially, its tumor inhibitory properties. As an important perspective, we will experimentally combine these strategies with those recently described by us with regard to the important antiangiogenic-antitumor effects of Trypanosoma cruzi calreticulin. Since the molecular targets of these strategies are most likely different, additive or synergic effects are envisaged.