Photic Response Parameters of Circadian Rhythms in The Spinifex Hopping Mouse, Notomys alexis.

Circadian rhythms are generated endogenously by biological clocks or 'pacemakers', which are responsive to significant environmental stimuli termed zeitgebers. Interactions between pacemakers and zeitgebers provide the basis for synchronisation by light-dark (LD) cycles, and the characteristics of each of these elements determines the phase-relations maintained between an animal's circadian activity rhythms and the natural temporal environment. We report here the basic photic response parameters for an Australian native rodent, Notomys alexis. Under controlled conditions of constant darkness or constant light, N. alexis were found to 'free-run', and with periods different from 24 hours. Under LD cycles N. alexis were strictly nocturnal although, compared to other rodents, entrainment to LD cycles was relatively unstable. This may indicate that N. alexis are not strongly dependent on the LD cycle as a zeitgeber.

Functional role of GABA in cat retina: I. Effects of GABAA agonists

Putative GABAergic mechanisms were studied in perfused cat retina by means of intracellular recording and application of GABA and the GABAA agonists δ-amino valeric acid (dAVA), muscimol, and THIP. In contrast to results reported previously for cold-blooded vertebrates, introduction of 20 mM GABA into the superfusate had no influence upon the response properties of cat retinal horizontal cells (HCs). In common with results reported in cold-blooded vertebrates, introduction of the GABAA agonists dAVA (2–12 mM) and THIP or muscimol (0.2–1 mM) had four consistent reversible influences upon the response properties of cat retinal HCs: (1) they reduced photic-response amplitude, (2) slowed response onset, (3) slowed response offset, and (4) depolarized the dark membrane potential. Both rod and cone signal components were affected. GABAA agonists had similar influences upon both the time course and amplitude of responses recorded from amacrine and ganglion cells. In all cell types examined, the influence upon response kinetics was made particularly apparent with rapidly flickering stimuli. Flicker responses were reduced in amplitude much more than sustained responses. These results suggest that, in addition to other influences, GABAergic action serves to modify the time course of photic responses in both the inner and outer plexiform layer of mammalian retina making responses slower and less phasic.