The anatomical record : advances in integrative anatomy and evolutionary biology
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Postinjury inflammation has been implicated in secondary degeneration following injury to the spinal cord. The cellular inflammatory response to injury has not been described in the lateral compression injury model, although various types of compression injuries account for ∼20% of human spinal cord injuries (SCI). Here, we used forceps to induce a moderate compression injury to the thoracic spinal cord of female Sprague-Dawley rats. ⋯ The expression of MHC class II antigens is necessary for the initiation of adaptive immunity and was accompanied by an influx of T cells. T cells were initially restricted to gray matter at the injury epicenter but were later observed throughout the lesioned parenchyma. In summary, we demonstrate that lateral forceps compression of the spinal cord produces a neuroinflammatory response similar to that described in human spinal cord trauma and in other experimental models of spinal cord trauma, thus is an appropriate model to study secondary neurodegeneration in SCI.
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This study concerns the morphological differentiation between double outlet right ventricle (DORV) and aortic dextroposition (AD) defects, namely tetralogy of Fallot and Eisenmenger anomaly. Indeed, despite the similar condition in terms of sequential ventriculo-arterial connections, DORV and AD are two distinct morphological entities. ⋯ Emphasis is also given to the association of straight parallel great arteries conotruncal malformations, DORV and transposition of the great arteries, with the asplenia type of heterotaxy laterality defects. Within this context, the absence of subaortic ventricular septal defect and concomitantly of spiraliform great arteries in the asplenia group of heterotaxy anomalies, as detected by this study, further substantiates our belief of not mixing collectively the ADs with the DORV in clinico-pathological diagnosis.
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Comparative Study
Comparative study of trans-oral and trans-tracheal intratracheal instillations in a murine model of acute lung injury.
Animal model is of importance to further elucidate the pathogenesis of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). We envisioned a possibility that there might be the differences in lipopolysaccharide (LPS)-induced acute lung inflammation by the trans-oral and trans-tracheal intratracheal instillations. We compared the LPS-induced early inflammatory responses by these two methods. ⋯ More IL-8 is produced from A549 cells than from NCI-H292 cells under the treatment of LPS. The increased IL-8 release in the BAL fluid and enhanced inflammatory responses caused by LPS may be due to more LPS delivered into the alveolar spaces by the trans-tracheal intratracheal instillation compared to the trans-oral one. The trans-tracheal intratracheal instillation is proved to be more suitable to establish the murine model of ALI than the trans-oral one and helpful to further elucidate the pathogenesis of ALI/ARDS.
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Dorsal sagittal venous sinus (DSVS) is an encephalic structure located in the midline of brain dorsal surface, starting behind the frontal venous sinus and following the brain falx in its extension. Knowing DSVS morphology and cranial-cerebral relationships it is very important for surgeon when he is planning the placement of craniotomies, in order to prevent the damage of this structure. The main purpose of this study were to establish craniometric points that can be used as key points of neurosurgical importance providing an anatomic framework to brain access regarding the localization of DSVS, and to characterize the morphology of DSVS in the three groups considered in study according their type of skull (brachycephalic-B, dolychocephalic-D and mesocephalic-M). ⋯ From the three groups, DSVS length and width were different, his geometry in B assumed a triangular appearance and in D, M a "butterfly" shape. From all craniometric points considered, only bregma (br) can be useful as a landmark to delimitate DSVS morphology in all three groups. Asterion in M, stephanion in B, glabella and pterion in all three groups, can not be used to compose a framework that help to understand skull surface projection of DSVS morphology, since their measurements were not uniform.
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The mechanisms underlying neuropathic pain induction are very complex but might involve abnormal spontaneous activity in the sensory dorsal root ganglion (DRG). Voltage-gated sodium channels in the DRG are essential for the genesis of abnormal spontaneous neuronal activity. In this study, we examined the changes in expression of the voltage-gated sodium channel Nav1.1 in the DRG after peripheral nerve injury. ⋯ Immunohistochemical study further confirmed a marked increase in the percentage of Nav1.1-positive cells in the ipsilateral DRG on Day 3 after fifth lumbar spinal nerve ligation. Similarly, on Day 7 after sciatic nerve axotomy, the amount of Nav1.1 protein and the percentage of Nav1.1-positive cells in the ipsilateral L5 DRG were also significantly increased. Our results suggest that an early increase in DRG Nav1.1 expression after peripheral nerve injury might be involved in the induction of neuropathic pain.