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Chronic pain is common in our population, and most of these patients are inadequately treated, making the development of safer analgesics a high priority. Knee osteoarthritis (OA) is a primary cause of chronic pain and disability worldwide, and lower extremity OA is a major contributor to loss of qualityadjusted life-years. In this study we tested the hypothesis that a novel JDNI8 replication-defective herpes simplex-1 viral vector (rdHSV) incorporating a modified carbonic anhydrase-8 transgene (CA8*) produces analgesia and treats monoiodoacetate-induced (MIA) chronic knee pain due to OA. We observed transduction of lumbar DRG sensory neurons with these viral constructs (vHCA8*) (~40% of advillin-positive cells and ~ 50% of TrkA-positive cells colocalized with V5-positive cells) using the intra-articular (IA) knee joint (KJ) route of administration. vHCA8* inhibited chronic mechanical OA knee pain induced by MIA was dose- and time-dependent. Mechanical thresholds returned to Baseline by D17 after IA KJ vHCA8* treatment, and exceeded Baseline (analgesia) through D65, whereas negative controls failed to reach Baseline responses. Weightbearing and automated voluntary wheel running were improved by vHCA8*, but not negative controls. Kv7 voltage-gated potassium channel-specific inhibitor XE-991 reversed vHCA8*-induced analgesia. Using IHC, IA KJ of vHCA8* activated DRG Kv7 channels via dephosphorylation, but negative controls failed to impact Kv7 channels. XE-991 stimulated Kv7.2-7.5 and Kv7.3 phosphorylation using western blotting of differentiated SH-SY5Y cells, which was inhibited by vHCA8* but not by negative controls. The observed prolonged dose-dependent therapeutic effects of IA KJ administration of vHCA8* on MIA-induced chronic KJ pain due to OA is consistent with the specific activation of Kv7 channels in small DRG sensory neurons. Together, these data demonstrate for the first-time local IA KJ administration of vHCA8* produces opioid-independent analgesia in this MIA-induced OA chronic pain model, supporting further therapeutic development. [ABSTRACT FROM AUTHOR]

To improve the low-load stable combustion capacity of a low-grade coal-fired boiler, this study proposed to reform C-layer secondary air, which was then used to improve the ignition and combustion stability of coal/airflow of a 600 MWe Foster Wheeler down-fired boiler. Cold airflow experiments and industrial measurements were carried out to investigate the influence of the new C-layer secondary air on the aerodynamic and combustion characteristics at low load under different C-layer secondary air ratios and damper openings, respectively. The flow and mixing characteristics of the C-layer secondary air and coal/airflow, the flue gas temperature and NOx, O2, and CO concentration distributions in the furnace at low load were examined. With increase in the C-layer secondary air ratio, the flow range of coal/airflow gradually expanded. The mixing distance first increased and then decreased. At an air ratio of 25%, the mixing distance was the longest. Industrial measurements showed that compared with that at the C-layer secondary air damper opening of 0%, the coal/airflow ignited earlier at 40% (corresponding to the C-layer secondary air ratio of 23.73%), and the flue gas temperature in the furnace increased substantially. At C-layer secondary air damper opening of 0%, 20%, and 40%, carbon content in the fly ash was 4.62%, 5.32%, and 4.20%, respectively. The respective NOx emissions at the furnace exits were 450 mg/Nm3, 378 mg/Nm3, and 427 mg/Nm3, (O2 = 6%). In actual operation, 40% is recommended as the optimal C-layer secondary air damper opening. [ABSTRACT FROM AUTHOR]

Mutations in superoxide dismutase 1 (SOD1) are responsible for 20% of familial ALS. Given the gain of toxic function in this dominantly inherited disease, lowering SOD1 mRNA and protein is predicted to provide therapeutic benefit. An early generation antisense oligonucleotide (ASO) targeting SOD1 was identified and tested in a phase I human clinical trial, based on modest protection in animal models of SOD1 ALS. Although the clinical trial provided encouraging safety data, the drug was not advanced because there was progress in designing other, more potent ASOs for CNS application. We have developed next- generation SOD1 ASOs that more potently reduce SOD1 mRNA and protein and extend survival by more than 50 days in [SOD1.sup.G93A] rats and by almost 40 days in [SOD1.sup.G93A] mice. We demonstrated that the initial loss of compound muscle action potential in [SOD1.sup.G93A] mice is reversed after a single dose of SOD1 ASO. Furthermore, increases in serum phospho-neurofilament heavy chain levels, a promising biomarker for ALS, are stopped by SOD1 ASO therapy. These results define a highly potent, new SOD1 ASO ready for human clinical trial and suggest that at least some components of muscle response can be reversed by therapy., Introduction Amyotrophic lateral sclerosis (ALS) is caused by the loss and dysfunction of neurons in motor pathways and leads to severe weakness, stiffness, and ultimately death in 3-5 years. Approximately [...]