Nervio interóseo posterior: origen, localización y trayecto nervioso: una revisión / Posterior interosseous nerve: origin, location and nerve path: a review

RESUMEN: El nervio interóseo posterior (NIP) ha sido utilizado como sinónimo ocontinuación inmediata del ramo profundo del nervio radial (RPNR) al emerger en el compartimiento posterior del antebrazo. Su origen tampoco es claro, describiéndose como nervio interóseo posterior a su trayecto proximal, intermedio o distal al músculo supinador. El objetivo de esta revisión es detallar la visión de diversos autores respecto al origen y trayecto del NIP, proponiendo una correcta terminología para estas estructuras. Se realizó una revisión bibliográfica de varios textos y de algunos artículos utilizados para la enseñanza de la anatomía humana, publicados entre los años 1800 y la actualidad. En la búsqueda, se determinaron criterios de inclusión que consideraban, anatomía humana, escritos en español, francés o inglés y que aludieran al NIP. Tras la exploración inicial se localizaron 18 libros, procedentes de Francia, Rusia, España, Argentina, Estados Unidos, Canadá, Reino Unido, Alemania, India y México. Una descripción del NIP más precisa, en cuanto al origen, trayecto y función, es aquella postulada por la vertiente francesa, correspondiendo a un origen terminal del ramo profundo del nervio radial, luego de emitir sus ramos musculares. Este delgado nervio transcurre adosado a la membrana interósea para luego avanzar por el cuarto compartimiento extensor, distribuyéndose en las articulaciones dorsales del carpo a quienes inerva sensitiva y propioceptivamente.

SUMMARY: The posterior interosseous nerve (PIN) has been used as a synonym or immediate continuation of the deep branch of the radial nerve as it emerges in the posterior compartment of the forearm. Its origin is not clear either, being described as a posterior interosseous nerve to its proximal, intermediate or distal path to the supinator muscle. The objective of this review is to detail the vision of various authors regarding the origin and path of the PIN, proposing a correct terminology for these structures. A bibliographic review of several texts and some articles used for the teaching of human anatomy, published between the 1800s and the present day, was carried out. In the search, inclusion criteria were determined that considered human anatomy, written in Spanish, French or English and that alluded to the PIN. After the initial exploration, 18 books were located, coming from France, Russia, Spain, Argentina, the United States, Canada, the United Kingdom, Germany, India and Mexico. A more precise description of the PIN, in terms of origin, path and function, is that postulated by the French literature, corresponding to a terminal origin of the deep branch of the radial nerve, after emitting its muscular branches. This thin nerve runs attached to the interosseous membrane to then advance through the fourth extensor compartment, distributing itself in the dorsal carpal joints to which it innervates sensitively and proprioceptively.

Inervación del músculo braquiorradial en individuos brasileños: aspectos anatomo-clínicos de la biometría de origen y distribución nerviosa / Innervation of the brachioradialis muscle in Brazilian individuals: anatomo-clinical aspects of the biometry of origin and nervous distribution

El nervio para el músculo braquiorradial (BR) ha sido utilizado en transferencias nerviosas para recuperaciones en funciones de la mano como consecuencias de lesiones que afectan el plexo braquial. Con el propósito de investigar el número y localización biométrica de los ramos primarios provenientes del nervio radial y puntos motores respecto un punto de referencia ubicado en la región del codo, se estudiaron 30 miembros superiores de individuos adultos brasileños, de la Universidad Estadual de Ciencias da Saúde de Alagoas, Maceió, Brasil. Las muestras se encontraban fijadas en solución de formaldehído al 10 %, de los cuales 15 miembros eran derechos y 15 izquierdos. Como punto de referencia se utilizó una línea que pasó a través de las partes más prominentes de los epicóndilos humerales, línea bi-epicondilea (LBE). Con respecto al origen nervioso para el músculo BR, todos los ramos se originaron a partir del nervio radial (NR). El promedio de la cantidad de Ramos Primarios (RP) fue de 1,53 (DS 0,73). En 18 muestras (60 %) se observó sólo un RP; en 8 casos (26,7 %) se encontraron 2 RP, mientras que en 4 casos (13,3 %) de la muestra se observaron 3 RP. Sobre la localización biométrica de los orígenes de los RP, es importante mencionar que todos se ubicaron proximal a la LBE. En promedio, estos se ubicaron a 38 mm (DS 0,9); 29 mm (DS 1,2) y 22 mm (DS 1,0) para el primer, segundo y tercer RP, respectivamente. En relación a los puntos motores (PM), en 4 casos (13 %) se observó 1 PM dado por la penetración directa de un ramo primario, en 13 casos (43 %) existieron 2 PM, en 8 casos (27 %) se encontraron 3 PM y en 5 casos (17 %) se observaron 4 PM. En tres casos (10 %) la inervación hacia el músculo BR emitió filetes nerviosos hacia el músculo extensor radial largo del carpo. Los resultados expuestos en esta investigación son un importante aporte para bloqueos nerviosos, estimulaciones eléctricas y transferencias nerviosas.

The nerve for the brachioradialis muscle (BR) has been used in nerve transfers for recoveries in functions of the hand as a consequence of lesions affecting the brachial plexus. With the purpose of investigating the number and biometric location of the primary branches coming from the radial nerve and motor points with respect to a reference point located in the elbow region, thirty upper limbs of Brazilian adult individuals from the State University of Sciences of Saúde de Alagoas, Maceió, Brazil were used. The samples were fixed in 10 % formaldehyde solution, of which 15 were right and 15 left. As a reference point, a line was used that passed through the most prominent parts of the humeral epicondyls, bi-epicondilar line (BEL). With respect to the nervous origin for the BR muscle, all the branches originated from the radial nerve (RN). The average number of primary branches (PB) was 1.53 (SD 0.73). In 18 samples (60 %) only one PB was observed; in 8 cases (26.7 %) 2 PB were found, while in 4 cases (13.3 %) of the sample 3 PB were observed. Regarding the biometric location of the origins of PB, it is important to mention that all were located proximal to the BEL. On average, these were located at 38 mm (SD 0.9); 29 mm (DS 1.2) and 22 mm (DS 1.0) for the first, second and third PB, respectively. In relation to the motor points (MP), in 4 cases (13 %) 1 MP was observed as direct penetration of the PB, in 13 cases (43 %) there were 2 MP, in 8 cases (27 %) they found 3 MP and in 5 cases (17 %) 4 MP were observed. In three cases (10 %) the innervation towards the BR muscle emitted nerve fillets towards the extensor carpi radialis longus muscle. The results presented in this investigation are an important contribution to nerve blocks, electrical stimulations and nerve transfers.

Inervación del músculo extensor radial largo del carpo en individuos brasileños: biometría de su origen y distribución / Innervation of the extensor carpi radialis longus muscle in Brazilian individuals: biometry of its origin and distribution

El músculo extensor radial largo del carpo (MERLC) es un músculo localizado en el compartimiento posterior (extensor-supinador) del antebrazo y tiene gran importancia en el cierre del puño. Hay pocos estudios biométricos con respecto al punto de origen de sus ramos de inervación, así como sobre la distribución de los mismos. Basado en lo anterior, se estudiaron 30 miembros superiores, formolizados, de individuos adultos Brasileños, de la Facultad de Medicina de la Universidad Estadual de Ciencias da Saúde de Alagoas, Maceió, Brasil. Luego de localizar el nervio, se midió la distancia entre el origen del ramo primario y el de los puntos motores respecto a la línea biepicondílea (LBE), los cuales fueron visualizados y disecados utilizando una lupa. El nervio en cuestión, se observó a nivel del brazo o proximal a LBE en 28 casos (93 %) y los 2 restantes a nivel de esta línea (7 %). Los ramos para el ERLC se originaron a partir del nervio radial, observando un ramo primario en 20 miembros (80 %), y en los restantes 10 (20 %) se observaron 2 ramos primarios, promediando 1,3 ramos (DS 0,5). El origen más proximal del primer ramo primario (RP) independiente de que si existían 1 o 2 fue en promedio 3 cm (DS 1,0) proximal a LBE. El PM más distal, se ubicó distal a LBE en 24 casos con un promedio de 1,9 cm (DS 1,0); localización a nivel de LBE en 3 casos. Sólo en 3 casos el PM más distal se encontró proximal a LBE, en un promedio de 0,8 cm (DS 0,5). La distribución de puntos motores fue variable, ya que muchas veces los RP se bifurcaban en ramos secundarios y éstos, a su vez se dividían hasta 6 veces en ramos terciarios que penetraban en el músculo. El conocimiento biométrico del origen del nervio del MERLC, así como su distribución, es un aporte importante al área anátomo-quirúrgica, así como, su utilización en bloqueos nerviosos, transferencias nerviosas y zonas de ubicación de electrodos con propósitos de estimulación eléctrica en pacientes que necesiten rehabilitar la acción de musculatura extensora radial lesionada.

The extensor carpi radialis longus muscle (ECRLm) is located in the posterior compartment (extensorsupinator) of the forearm and has great importance in the closure of the hand. There are few biometric studies with respect to the point of origin of their branches of innervation, as well as on the distribution of them. For this study, 30 upper limbs, formalized, of Brazilian adult individuals were used, from the Faculty of Medicine of the Universidad Estadual de Ciencias da Saúde de Alagoas, Maceió, Brazil. After locating the nerve, we measured the distance between the origin of the primary branch and that of the motor points with respect to biepicondilar line (BEl), which were visualized and dissected using a magnifying glass. The nerve in question was observed at the level of the arm or proximal to BEl in 28 cases (93 %) and the remaining 2 at the level of this line (7 %). The branches for the ECRLm originated from the radial nerve, observing a primary branch in 20 limbs (80 %), and in the remaining 10 (20 %) two primary branches were observed, averaging 1.3 branches (SD 0.5). The most proximal origin of the first primary branch (PB) independent of whether there was 1 or 2 was on average 3 cm (SD 1.0) proximal to BEl. The most distal MP was distal to BEl in 24 cases with an average of 1.9 cm (SD 1.0); location at the BEl level in 3 cases. Only in 3 cases was the most distal MP found proximal to BEl, an average of 0.8 cm (SD 0.5). The distribution of motor points was variable, since many times the PB bifurcated into secondary branches and these, in turn, could divide up to 6 times in tertiary branches that penetrated in the muscle. The biometric knowledge of the origin of the nerve of the ECRLm, as well as its distribution, is an important contribution to the anatomo-surgical area, as well as its use in nerve blocks, nerve transfers and electrode placement areas for purposes of electrical stimulation in patients they need to rehabilitate the action of injured radial extensor musculature.

Inervación del músculo extensor radial corto del carpo en individuos brasileños: biometría de su origen y distribución / Innervation of the extensor carpi radialis brevis muscle in Brazilian individuals: biometry of its origin and distribution

El ramo de inervación para el músculo extensor radial corto del carpo (MERCC) ha sido utilizado para restablecer funciones de la musculatura del miembro superior en pacientes con lesiones medulares, del plexo braquial o de sus ramos terminales. El origen del nervio para el MERCC es variable, pudiendo originarse desde el tronco del nervio radial (NR), del ramo profundo de este nervio (RPNR) o del ramo superficial del mismo (RSNR). Con el propósito de complementar la anatomía sobre el origen y distribución del ramo para el MERCC, se utilizaron 30 miembros superiores, formolizados, de cadáveres de individuos Brasileños, localizados en los laboratorios de Anatomía de la Universidad Estadual de Ciencias da Saude, Maceió, Brasil. A través de disección se localizó el músculo y su inervación, determinando su origen, así como su distribución. Para efectuar la biometría, se consideró como referencia una línea transversal que pasaba entre las partes más prominentes de los epicóndilos lateral y medial del húmero (LBE), registrando la distancia entre esta línea y el punto de origen de este ramo muscular, así como la distancia entre la LBE y los puntos motores. El nervio para el MERCC se originó del RPNR en 50 % de los casos; desde el tronco principal del NR en 26, 7 % y desde el RSNR en 23, 3 %. La distancia entre el origen del ramo en estudio y la LBE fue en promedio de 23 ± 12 mm; la distancia entre el 1º, 2º y 3º punto motor respecto a la LBE fue de 55 ± 17 mm, 66 ± 17 mm y 79 ± 11 mm, respectivamente. La distribución de la inervación fue clasificada en 4 tipos en relación a sus puntos motores. Los resultados obtenidos son un importante aporte al conocimiento anatómico, así como a la neurocirugía en las transferencias nerviosas con propósitos de restauración de las funciones de músculos lesionados en el miembro superior.

The branch of the innervation for the extensor carpi radialis brevis muscle (ECRBm), has been used to reestablish muscle functions in the upper limbs of patients who have spinal cord injury, of the brachial plexus or its terminal branches. The origin of the ECRBm varies, and can originate from the trunk of the radial nerve (RN), from the deep branch of the radial nerve (DBRN), or from the superficial branch of the radial nerve (SBRN). In order to further complement the anatomy related to the origin and distribution of the ECRBm branch, 30 formolized upper limbs from Brazilian individuals, from the Universidad Estadual de Ciencias da Saude, Maiceió, Brazil were used. Through dissection, the muscle and its innervations was located, determining the origin of the branch as well as distribution. To determine biometry, a transversal reference line, which passed through the most prominent areas of the epicondyles of the humerus (BEL) was considered. The nerve for ECRBm originated from DBRN in 50 % of cases; from the main trunk of RN in 26.7 % and from SBRN in 23.3 %. The distance from the origin of the branch studied and the BEL was an average of 23 ± 12 mm; the distance from the first, second and third motor point to the BEL was 55 ± 17 mm, 66 ± 17 mm and 79±11 mm, respectively. The distribution of the innervation was classified in four types in relation to the motor points. The results are an important contribution to anatomical knowledge, as well as neurosurgery during nerve transfers to restore functions of damaged muscles in the upper limb.

Breaking the glass ceiling: structural, cultural, and organizational barriers preventing women from achieving senior and executive positions.

The business case for gender diversity in senior and executive positions is compelling. Studies show that companies that have the best records for promoting women outstrip their competition on every measure of profitability. Yet women disproportionately are failing to attain high-level positions. Reviewing current data on women in the workplace, findings of studies on the relationship between gender diversity in senior management and company performance, and the literature on gender behavioral differences and the workplace, this article explores the possible reasons for the persistent wage and gender gap between women and men in senior leadership positions and discusses possible remedies.

Exostosis costal como causa de hemoptisis / No disponible

No disponible

Hemorragia digestiva alta en varón homosexual con infección por el virus de la inmunodeficiencia humana / No disponible

No disponible

Hypertrophy of vascularized bone isograft in rats treated with cyclosporine A.

The aim of this study was to investigate the effects of cyclosporine A (CsA) on vascularized tibio-fibula isograft between 12-week-old male Lewis rats. After transplantation, 45 rats were randomly allocated to one of the following 7 treatment groups: (1) 4-week vehicle (n = 5), (2) 4-week CsA (n = 5), (3) 8-week vehicle (n = 10), (4) 8-week CsA (n = 10), (5) 4-week CsA followed by 4-week vehicle (n = 5), (6) 16-week vehicle (n = 5), or (7) 4-week CsA followed by 12-week vehicle (n = 5). In soft X-ray and micro-computed tomography examination, hypertrophic change of the grafted bones was apparent in the 4- and 8-week CsA groups. Mineral apposition rate and bone formation rate of the grafted bones in the 4-week CsA group were markedly higher than those in the 4-week vehicle group. In the 4- and 8-week CsA groups, however, bone mineral density (BMD) of the grafted bones was lower and strength of the reconstructed bones was weaker than the 4- and 8-week vehicle groups. Urinary deoxypyridinoline (DPD) level was higher in the 4- and 8-week CsA groups than in the 4- and 8-week vehicle groups. The group of 4-week CsA followed by 4-week vehicle had a level of urinary DPD equal to the 8-week vehicle group, but their BMD of the grafted bones was lower and strength of the reconstructed bones was weaker than the 8-week vehicle group. By contrast, the group of 4-week CsA followed by 12-week vehicle had BMD of the grafted bones and strength of the reconstructed bones similar to the 16-week vehicle group. These findings demonstrate that short-term CsA treatment induces hypertrophic change of vascularized bone graft with high-turnover bone loss, and strength of the reconstructed bone is gradually restored after the cessation of CsA treatment.

Effects of vitamin D analog, 22-oxa-1,25-dihydroxyvitamin D(3), on bone reconstruction by vascularized bone allograft.

We previously reported that vascularized bone allograft using immunosuppressants, such as cyclosporine A (CsA), is one approach for reconstruction of large bone defects in both experimental animals (Microsurgery 15:663; 1994) and clinically in humans (Lancet 347:970, 1996). Because immunosuppressive agents such as CsA induce significant side effects, including bone loss, other therapeutic agents supporting successful vascularized bone allografts have been sought after. We investigated the effects of 22-oxa-1,25-dihydroxyvitamin D(3) (OCT) on vascularized bone allograft, and compared its effects with CsA. Twelve-week-old DA rats with the major histocompatibility antigen (MHC) RT-1(a) were used as donors and age-matched Lewis rats with MHC RT-1(l) used as recipients. Allografted bones in rats treated with vehicle were rejected completely. Soft X-ray examination demonstrated that administration of OCT (0.5 microg/kg per day) for 12 weeks after bone graft induced bone union as effective as treatment for 12 weeks with CsA (10 mg/kg per day). Transplanted bones in OCT-treated rats showed higher bone mineral density than that in CsA-treated rats. Histologically, transplanted bones in OCT-treated rats at 12 weeks were nonvital, but these bones united with recipient vital bones. After cessation of 12 week treatment with OCT, new bone formation occurred around the grafted nonvital bones during a 9 month period. Transplanted bones in CsA-treated rats were vital and formed union with recipient bones, whereas cortical bones became thin when compared with nonvital bones in OCT-treated rats. Urinary deoxypyridinoline levels in rats treated with CsA were significantly higher than levels in rats treated with OCT, suggesting accelerated bone resorption in CsA-treated rats. These results suggest that OCT exerts an anabolic action on bone reconstruction by allogeneic bone transplantation.

Regulation of Cbl molecular interactions by the co-receptor molecule CD43 in human T cells.

CD43, one of the most abundant glycoproteins on the T cell surface, has been implicated in selection and maturation of thymocytes and migration, adhesion, and activation of mature T cells. The adapter molecule Cbl has been shown to be a negative regulator of Ras. Furthermore, it may also regulate intracellular signaling through the formation of several multi-molecular complexes. Here we investigated the role of Cbl in the CD43-mediated signaling pathway in human T cells. Unlike T cell receptor signaling, the interaction of the adapter protein Cbl with Vav and phosphatidylinositol 3-kinase, resulting from CD43-specific signals, is independent of Cbl tyrosine phosphorylation, suggesting an alternative mechanism of interaction. CD43 signals induced a Cbl serine phosphorylation-dependent interaction with the tau-isoform of 14-3-3. protein. Protein kinase C-mediated Cbl serine phosphorylation was required for this interaction, because the PKC inhibitor RO-31-8220 prevented it, as well as 14-3-3 dimerization. Moreover, mutation of Cbl serine residues 619, 623, 639, and 642 abolished the interaction between Cbl and 14-3-3. Overexpression of Cbl in Jurkat cells inhibited the CD43-dependent activation of the mitogen-activated protein kinase (MAPK) pathway and AP-1 transcriptional activity, confirming nevertheless a negative role for Cbl in T cell signaling. However, under normal conditions, PKC activation resulting from CD43 engagement was required to activate the MAPK pathway, suggesting that phosphorylation of Cbl on serine residues by PKC and its association with 14-3-3 molecules may play a role in preventing the Cbl inhibitory effect on the Ras-MAPK pathway. These data suggest that by inducing its phosphorylation on serine residues, CD43-mediated signals may regulate the molecular associations and functions of the Cbl adapter protein.

T cell activation through the CD43 molecule leads to Vav tyrosine phosphorylation and mitogen-activated protein kinase pathway activation.

CD43, the most abundant membrane protein of T lymphocytes, is able to initiate signals that lead to Ca2+ mobilization and interleukin-2 production, yet the molecular events involved in signal transduction pathway of the CD43 molecule are only beginning to be understood. We have shown recently that cross-linking CD43 on the cell surface of human T lymphocytes with the anti-CD43 monoclonal antibody L10 leads to CD43-Fyn kinase interactions and to Fyn phosphorylation on tyrosine residues. This interaction seems to be mediated by the SH3 domain of Fyn and a proline-rich sequence located in the cytoplasmic domain of CD43. Here we show that CD43-specific activation of human T lymphocytes induced tyrosine phosphorylation of the adaptor protein Shc and of the guanine exchange factor Vav, as well as the formation of a macromolecular complex that comprises Shc, GRB2, and Vav. CD43 ligation resulted in enhanced formation of Vav.SLP-76 complexes and in the activation and nuclear translocation of ERK2. Cross-linking of the CD43 molecule in 3T3-CD43(+) cells induced luciferase activity from a construct under the control of the Fos serum responsive element. Altogether, these data suggest that the mitogen-activated protein kinase pathway is involved in CD43-dependent interleukin-2 gene expression.

CD43-specific activation of T cells induces association of CD43 to Fyn kinase.

CD43, the most abundant membrane protein of T lymphocytes, is able to initiate signal transduction pathways that lead to Ca2+ mobilization and interleukin-2 production, yet the molecular events involved in CD43's signal transduction pathway are poorly understood. In the present report we show that activation of both purified T lymphocytes and Jurkat cells, through CD43 cross-linking with the anti-CD43 L10 monoclonal antibody, induced CD43 association to Fyn kinase. This association is mediated by the Src homology 3 (SH3) domain of Fyn, since a glutathione S-transferase-Fyn SH3 fusion protein was able to precipitate CD43 from lysates of CD43-activated T cells. A synthetic peptide containing the SH3 binding sites of p85, located within the amino acid sequence 300ERQPAPALPPKPPKP314, was able to inhibit binding of CD43 to Fyn as well as to the glutathione S-transferase-Fyn SH3 fusion protein. We also provide evidence that upon CD43 cross-linking, Fyn is tyrosine-phosphorylated in a time-dependent manner. Our results suggest that CD43 cross-linking on the T cell surface induces the interaction between CD43 and Fyn, presumably through the Fyn SH3 domain and a putative SH3 binding site in CD43, leading to Fyn tyrosine phosphorylation and signal propagation.