, 1993 and Sharshar et al., Tyrosine Kinase Inhibitor Library research buy 2005). Moreover, surface electrodes have previously been validated against diaphragm needle EMG (Demoule et al., 2003a) and we were anyway reluctant to use the latter technique because of the risk of pneumothorax during inspiratory effort and in the context of positive pressure

ventilation. A related issue is the possibility that changes in the position of the diaphragm relative to the electrodes during NIV could have influenced the response to TMS although the difference between esophageal pressures was not large. TMS responses were therefore normalized to the response to phrenic nerve stimulation to minimize the impact of any peripheral changes. Ideally we would have performed paired stimulations at a range of interstimulus intervals to produce an interstimulus response curve as described previously (Demoule et al., 2003b, Sharshar et al., 2004a and Sharshar et al., 2004b). However, this would have considerably increased both the number of stimulations and the duration of the study, so we chose to use only the two interstimulus intervals shown previously to produce the greatest inhibition and facilitation (Hopkinson et al., 2004). Again, to reduce the number of stimulations administered we did not formally assess the motor threshold for the rectus abdominis. However, we have found previously that rectus abdominis threshold in response to stimulation at the vertex

is similar to that of the diaphragm both in COPD patients and controls (Hopkinson

et al., 2004). A further consideration is that in contrast to the diaphragm, it is Veliparib research buy not possible to perform peripheral supramaximal stimulation of the abdominal muscles in a manner that is likely to be acceptable to patients (Hopkinson et al., 2010 and Suzuki et al., 1999) so it was not possible to normalize the MEP response to allow for any changes in peripheral conduction that might have occurred. In summary we conclude that a requirement for long-term home NIV in COPD is not associated with changes in the excitability (-)-p-Bromotetramisole Oxalate of corticospinal pathways to the respiratory muscles. However we did find, taking the group as a whole, that the facilitatory and inhibitory properties of the intracortical circuits of the diaphragm motor cortex were strongly correlated with inspiratory muscle strength and hypercapnia respectively. While we are cautious in over interpreting the former result we speculate that prolonged exposure to hypercapnia results in greater intracortical inhibition: this could contribute to the pathogenesis of respiratory failure in COPD. Finally, the acute application of NIV did not, in contrast to our previous findings in healthy subjects, alter the facilitatory and inhibitory properties of the diaphragm motor cortex as judged by the response to paired TMS, indicating likely long-term reorganisation of the cortex as a consequence of COPD. The authors have no conflict of interest.