Neurorestoratology evidence in an animal model with cervical spondylotic myelopathy

published_or_final_versio

A combination of functional magnetic resonance imaging and diffusion tensor image to explore structure-function relationship in healthy and myelopathic spinal cord

published_or_final_versio

Proton Density-weighted Spinal fMRI Comparison between Sensorimotor Task and Acupoint Stimulation

Proton density-weighted fMRI studies have been carried out in spinal cord in the current study. We compared the spinal cord activation produced by handgripping sensorimotor task and electro-acupuncture stimulation. Activation was detected in both cases localized at spinal levels C6-C7 (11/14 in sensorimotor and 7/11 in acupuncture stimulation). It was observed that the amount of activation in sensorimotor task was in general greater than in electroacupuncture stimulation. The percentage signal changes were found to be similar. Our results indicate that proton density-weighted fMRI in low field MRI system can be used for sensorimotor and acupuncture pathway research.published_or_final_versio

Is the speed of chronic compression an important factor for chronic spinal cord injury rat model?

postprin

Measurement of Cosmic-ray Muons and Muon-induced Neutrons in the Aberdeen Tunnel Underground Laboratory

We have measured the muon flux and production rate of muon-induced neutrons at a depth of 611 m water equivalent. Our apparatus comprises three layers of crossed plastic scintillator hodoscopes for tracking the incident cosmic-ray muons and 760 L of gadolinium-doped liquid scintillator for producing and detecting neutrons. The vertical muon intensity was measured to be $I_{\mu} = (5.7 \pm 0.6) \times 10^{-6}$ cm$^{-2}$s$^{-1}$sr$^{-1}$. The yield of muon-induced neutrons in the liquid scintillator was determined to be $Y_{n} = (1.19 \pm 0.08 (stat) \pm 0.21 (syst)) \times 10^{-4}$ neutrons/($\mu\cdot$g$\cdot$cm$^{-2}$). A fit to the recently measured neutron yields at different depths gave a mean muon energy dependence of $\left\langle E_{\mu} \right\rangle^{0.76 \pm 0.03}$ for liquid-scintillator targets.Comment: 14 pages, 17 figures, 3 table

Switchable genome editing via genetic code expansion

Multiple applications of genome editing by CRISPR-Cas9 necessitate stringent regulation and Cas9 variants have accordingly been generated whose activity responds to small ligands, temperature or light. However, these approaches are often impracticable, for example in clinical therapeutic genome editing in situ or gene drives in which environmentally-compatible control is paramount. With this in mind, we have developed heritable Cas9-mediated mammalian genome editing that is acutely controlled by the cheap lysine derivative, Lys(Boc) (BOC). Genetic code expansion permitted non-physiological BOC incorporation such that Cas9 (Cas9BOC) was expressed in a full-length, active form in cultured somatic cells only after BOC exposure. Stringently BOC-dependent, heritable editing of transgenic and native genomic loci occurred when Cas9BOC was expressed at the onset of mouse embryonic development from cRNA or Cas9BOC transgenic females. The tightly controlled Cas9 editing system reported here promises to have broad applications and is a first step towards purposed, spatiotemporal gene drive regulation over large geographical ranges

Effect Of Combined Aerobic And Resistance Training On HPA Axis Reactivity In HIV+ Women Undergoing Treatment For Substance Abuse

Substance abuse and infection with human immunodeficiency virus (HIV) are chronic stressors that affect hypothalamic-pituitary-adrenal (HPA) axis function. The purpose of this study was to investigate the effect of combined aerobic and resistance training on HPA axis reactivity in women with HIV undergoing treatment for substance abuse. Sixteen women (mean ± SD; 41 ± 9 years, 164 ± 6 cm, 78.1 ± 17.1 kg, 36 ± 10 % body fat) infected with HIV and enrolled in an intensive 60-day in-patient substance addiction/abuse treatment program were recruited shortly after admission to the treatment facility. Participants were assigned to one of two groups using randomization: (1) supervised combined aerobic and resistance exercise sessions 3 times per week (EX) for six weeks or (2) no exercise training (Control) for six weeks. Before (PRE) and after (POST) the 6-week period participants completed a 10-min public speaking task (Trier Social Stress Test). Saliva samples were obtained before (baseline), immediately after, and every 10 min for 50 min after the task. Saliva samples were analyzed for cortisol. HPA axis reactivity was determined as the difference between the highest values after the test minus the baseline value. HPA axis reactivity did not differ between groups at PRE (EX: 1.9 ± 2.0 nmol•L-1; Control: 1.1 ± 2.7 nmol•L-1) or POST (EX: 1.7 ± 2.1 nmol•L-1; Control: 0.0 ± 1.3 nmol•L-1). Similarly no differences were found between PRE and POST although the reactivity for the Control group appeared to be reduced at POST. HIV+ women in early recovery from substance abuse appear to display blunted HPA axis reactivity. A combined aerobic and resistance training intervention did not affect this reactivity; although, the exercise intervention might have prevented a further decline in reactivity

Clinical correlation of nuclear survivin in esophageal squamous cell carcinoma

To examine the correlation of survivin (both total and nuclear survivin) with clinicopathological parameters of esophageal squamous cell carcinoma (ESCC) patients. Tumors and non-tumor tissues near the proximal resection margins were resected from ESCC patients undergone esophagectomy. Quantitative polymerase chain reaction (qPCR) was performed to detect survivin mRNA expression level in the 10 paired tumor and adjacent non-tumor tissues. To confirm with the clinical situation, survivin mRNA and protein expression were measured by qPCR and immunoblot, respectively, in 5 ESCC cell lines and a non-neoplastic esophageal epithelial cell line. Immunohistochemistry was employed to reveal the cellular localization of survivin in tumor tissues isolated from the 64 ESCC patients undergone surgery alone. Up-regulation of survivin mRNA and protein was found in 5 ESCC lines (HKESC-1, HKESC-2, HKESC-3, HKESC-4, and SLMT-1) when compared to a non-neoplastic esophageal epithelial cell line NE-1. In particular, HKESC-3, HKESC-4, and SLMT-1 cells demonstrated ~50-fold increase in survivin mRNA. High level of survivin mRNA in tumor tissues when compared to non-tumor tissues was found in 70 % (7 of 10) of clinical cases. The increase in expression ranged from ~twofold to ~16-fold. Immunohistochemistry results showed that survivin was found at the cell nuclei in all specimens examined. Nuclear expression of survivin was inversely associated with the likelihood of developing nodal metastasis (p = 0.021) and significantly associated with early-stage ESCC (p = 0.039). Nuclear survivin could serve as a marker for indicating disease status in ESCC patients. © 2012 The Author(s).published_or_final_versio