Characterizing Neutron-Proton Equilibration in Nuclear Reactions with Subzeptosecond Resolution.

We study neutron-proton equilibration in dynamically deformed atomic nuclei created in nuclear collisions. The two ends of the elongated nucleus are initially dissimilar in composition and equilibrate on a subzeptosecond time scale following first-order kinetics. We use angular momentum to relate the breakup orientation to the time scale of the breakup.

Sensing muscle ischemia: coincident detection of acid and ATP via interplay of two ion channels.

Ischemic pain--examples include the chest pain of a heart attack and the leg pain of a 30 s sprint--occurs when muscle gets too little oxygen for its metabolic need. Lactic acid cannot act alone to trigger ischemic pain because the pH change is so small. Here, we show that another compound released from ischemic muscle, adenosine tri-phosphate (ATP), works together with acid by increasing the pH sensitivity of acid-sensing ion channel number 3 (ASIC3), the molecule used by sensory neurons to detect lactic acidosis.

A molecular sensor for the baroreceptor reflex?

The reflex that provides rapid neural control of blood pressure is triggered by an unknown molecular pressure sensor. ASIC2, an ion channel in a family that includes a mechanosensor from C. elegans, is shown by Lu et al.

Cutaneous sensory neurons expressing the Mrgprd receptor sense extracellular ATP and are putative nociceptors.

Sensory neurons expressing the Mrgprd receptor are known to innervate the outermost living layer of the epidermis, the stratum granulosum. The sensory modality that these neurons signal and the stimulus that they respond to are not established, although immunocytochemical data suggest they could be nonpeptidergic nociceptors. Using patch clamp of dissociated mouse dorsal root ganglion (DRG) neurons, the present study demonstrates that Mrgprd+ neurons have several properties typical of nociceptors: long-duration action potentials, TTX-resistant Na(+) current, and Ca(2+) currents that are inhibited by mu opioids.