Sensory reinnervation of muscle spindles after repair of tibial nerve defects using autogenous vein grafts.

Motor reinnervation after repair of tibial nerve defects using autologous vein grafts in rats has previously been reported, but sensory reinnervation after the same repair has not been fully investigated. In this study, partial sensory reinnervation of muscle spindles was observed after repair of 10-mm left tibial nerve defects using autologous vein grafts with end-to-end anastomosis in rats, and functional recovery was confirmed by electrophysiological studies. There were no significant differences in the number, size, or electrophysiological function of reinnervated muscle spindles between the two experimental groups.

Prognostic value of the microRNA-29 family in patients with primary osteosarcomas.

The aim of this study was to facilitate and deepen the understanding of the associations of the microRNA-29 (miR-29) family with tumor progression and patients' prognosis of primary osteosarcoma. We examined expression levels of miR-29a, miR-29b, and miR-29c in tumor tissues and patients' sera of 80 cases of primary osteosarcomas by quantitative real-time reverse transcriptase-polymerase chain reaction. The correlations of their serum levels with clinicopathological characteristics and patient prognosis were also analyzed.

Axon terminals expressing vesicular glutamate transporter VGLUT1 or VGLUT2 within the trigeminal motor nucleus of the rat: origins and distribution patterns.

Little is known about the significance of the two types of glutamatergic neurons (those expressing vesicular glutamate transporter VGLUT1 or VGLUT2) in the control of jaw movements. We thus examined the origin and distribution of axon terminals with VGLUT1 or VGLUT2 immunoreactivity within the trigeminal motor nucleus (Vm) in the rat. The Vm was divided into the dorsolateral division (Vm.

Vesicular glutamate transporter-immunoreactivities in the vestibular nuclear complex of rat.

Objective Aims to delineate the distribution profile of three isoforms of vesicular glutamate transporter (VGluT), viz. VGluT1-3, and their cellular localization within vestibular nuclear complex (VNC). Methods Brain sections from normal Sprague-Dawley rats were processed immunohistochemically for VGluT detection, employing avidin-biotinylated peroxidase complex method with 3-3'-diaminobenzidine (DAB) as chromogen.

Localization of vesicular glutamate transporters in the peripheral vestibular system of rat.

Objective: To examine the vesicular glutamate transporters (VGluTs: VGluT1-VGluT3) in the peripheral vestibular system.

Methods: The vestibular structures, including Scarpa's ganglion (vestibular ganglion, VG), maculae of utricle and saccule, and ampullary cristae, from normal Sprague-Dawley rats were processed immunohistochemically for VGluTs, by avidin-biotinylated peroxidase complex method, with 3-3'-diaminobenzidine (DAB) as chromogen.

Results: (1) VGluT1 was localized to partial neurons of VG and to the putative primary afferent fibers innervating vestibular end-organs.

VGluT1- and GAD-immunoreactive terminals in synaptic contact with PAG-immunopositive neurons in principal sensory trigeminal nucleus of rat.

Aim: To trace the origin of abundant vesicular glutamate transporter 1-like immunoreactive (VGluT1-LI) axon terminals in the dorsal division of the principal sensory trigeminal nucleus (Vpd) and the relationships between VGluT1-LI, as well as the glutamic acid decarboxylase (GAD)-LI axon terminals, and phosphate- activated glutaminase (PAG)-LI thalamic projecting neurons in the Vpd.

Methods: Following unilateral trigeminal rhizotomy, triple-immunofluorescence histochemistry for VGluT1, GAD and PAG and the immunogold-silver method for VGluT1 or GAD, combined with the immunoperoxidase method for PAG were performed, respectively.

Results: After unilateral trigeminal rhizotomy, the density of VGluT1-like immunoreactivity (IR) in the Vpd on the lesion side was reduced compared to its contralateral counterpart.

Medullary dorsal horn neurons providing axons to both the parabrachial nucleus and thalamus.

It has often been suggested that the trigemino- and spino-thalamic pathways are highly implicated in sensory-discriminative aspects of pain, whereas the trigemino- and spino-parabrachial pathways are strongly implicated in affective/emotional aspects of pain. On the other hand, the superficial laminae of the spinal dorsal horn, where many nociceptive neurons are distributed, have been reported to contain projection neurons innervating both the parabrachial nucleus (PBN) and thalamus by way of axon collaterals (Hylden et al., 1989).