67,70 Other brainstem nuclei are sensitive to pH and have been implicated in pll-mediated ventilatory control; these regions include the medullary raphe nuclei, nucleus of the tractus solitarius, and locus coeruleus.67,69,71 Thus, multiple chemosensitive sites are possible. The CO2 sensitivity in panic patients, and the associations MK-1775 purchase between panic and ventilation, make it tantalizing to speculate that abnormalities in these chemosensitive neurons and receptors might contribute to panic attacks. Knowledge of pH-sensitive molecules in the brain and their physiological roles is rapidly growing, but much remains

to be learned. Inhibitors,research,lifescience,medical pH-sensitive receptors and respiratory chemosensation Understanding the molecules that underlie pH effects on ventilatory control Inhibitors,research,lifescience,medical could pave the way for understanding pH sensitivity in the brain in general. Thus far no single molecule has been found to be responsible for respiratory chemosensation. A number of molecules have the potential to detect falling pH and stimulate breathing.72 Members of the TWIK family are pH-sensitive73; a

subset, the TASK channels, have garnered attention as potential respiratory chemoreceptors. Because TASK channels help maintain membrane voltage near the resting potential, inhibiting these channels increases excitability and the likelihood of generating action potentials. Inhibitors,research,lifescience,medical TASK channels can be inhibited by small reductions in extracellular pH. For example, reducing pH by just 1/10th of a unit from pH 7.4 to pH 7.3 inhibits TASK-1.73 TASK-1 and TASK-3 are widely expressed in brain,74 while TASK-2 expression in brain is limited Inhibitors,research,lifescience,medical to a few brain stem nuclei, including the retrotrapezoid nucleus (RTN), which has been implicated in pH control of ventilation. Nevertheless, disrupting the genes encoding TASK-1, TASK-2, or TASK-3 in mice failed Inhibitors,research,lifescience,medical to eliminate the centrally mediated hypercapnic ventilatory response,74-76 suggesting that the

TASK channels are not required. However, some pH-sensitive responses were affected. Loss of TASK-1, TASK-3, or both reduced the pH sensitivity of cultured raphe neurons, but not that of RTN neurons.74 TASK-1 GBA3 disruption also reduced peripheral chemosensitivity to hypercapnia in the carotid body.75 Additionally, TASK-2 disruption in mice increased the respiratory response to mild hypercapnia (1.5 and 2% CO2), suggesting a modulatory role.76. pH-sensitive ion channels, G-protein coupled receptors, and intracellular signaling molecules Besides the TASK channels, a wide number of additional molecules might sense pH in the brain. Examples of pH-sensitive ion channels include transient receptor potential (TRP) channels,77 P2X receptors,78,79 voltage-dependent Ca2+ channels,80 N-methyl-D aspartate (NMDA) receptors,81 acid-sensing ion channels (ASICs),82-84 and inward rectifier K channels.