The 'inflammatory reflex' acts through efferent neural connections from the central nervous system to lymphoid organs, particularly the spleen, that suppress the production of inflammatory cytokines. Stimulation of the efferent vagus has been shown to suppress inflammation in a manner dependent on the spleen and splenic nerves. The vagus does not innervate the spleen, so a synaptic connection from vagal preganglionic neurons to splenic sympathetic postganglionic neurons was suggested. We tested this idea in rats. In a preparatory operation, the anterograde tracer DiI was injected bilaterally into the dorsal motor nucleus of vagus and the retrograde tracer Fast Blue was injected into the spleen. On histological analysis 7-9 weeks later, 883 neurons were retrogradely labelled from the spleen with Fast Blue as follows: 89% in the suprarenal ganglia (65% left, 24% right); 11% in the left coeliac ganglion; but none in the right coeliac or either of the superior mesenteric ganglia. Vagal terminals anterogradely labelled with DiI were common in the coeliac but sparse in the suprarenal ganglia, and confocal analysis revealed no putative synaptic connection with any Fast Blue-labelled cell in either ganglion. Electrophysiological experiments in anaesthetized rats revealed no effect of vagal efferent stimulation on splenic nerve activity or on that of 15 single splenic-projecting neurons recorded in the suprarenal ganglion. Together, these findings indicate that vagal efferent neurons in the rat neither synapse with splenic sympathetic neurons nor drive their ongoing activity.

Summary. Pollimyrus isidori's electric organ discharge (EOD) is of the pulse type. Patterns of EOD intervals were investigated prior to, during and following spawning behaviors as related with overt behaviors, and with the sound production by the nestbuilding male. Prior to the time of reproduction, isolated and socially interacting fish (n = 15) showed characteristic discharge interval patterns for resting, swimming, probing, hovering and hiding activities. Males (n = 8) and females (n = 6) did not differ in their mean EOD repetition rates during resting (11.6+2.5 Hz), nor Short Bursts/rain (less than 20 intervals of 8-13 ms). In interacting fish Long Bursts (greater than 20 intervals of 8-13 ms, lasting for more than 300 ms) were observed only during the attack and bite sequence.

The retinal fiber layer and the juxtaretinal portion of the optic nerve of goldfish have been studied with light and electron microscopy in order to determine whether the age-related order of fibers in the nerve originates in the retina.In the retina, no patent spaces (channels) were noted. The fibers ran in fascicles and consisted of two classes: nonmyelinated fibers, which ran superficially (close to the vitreal surface), and "myelinated" fibers, which ran more deeply and were loosely wrapped by processes presumed to be glial. The myelinated fibers were larger and presumably older. The nonmyelinated fibers are believed to be the young ones, from the peripheral, more recently generated, ganglion cells, for the following reasons.(1) Their size and cytoskeletal elements were typical of young axons. (2) They were the only axons in peripheral retina. (3) They were continuous with the nonmyelinated fibers in the nerve, previously shown to be the young ones. (4) When retinal axons were cut peripherally, the degenerating axons were in the superficial part of the fiber layer. (5) Growth cones, presumably from the newest ganglion cells, were always observed at the most superficial position in the fiber layer, in direct contact with the basal lamina of the inner limiting membrane superficially and nonmyelinated fibers deeply. The nonmyelinated fibers always clustered together in the retinal fiber layer and occupied the most central portion in the cross-section of the optic nerve head. Thus, the age-related organization of fibers in the nerve is established in the retina.These results are discussed in the context of growth, with the aim of evaluating the relative importance of four factors that might influence the intraretinal course of the growth cone. Its interactions with other fibers and with the basal lamina of the inner limiting membrane seem to be more important than interactions with the glial end feet or guidance into open, preformed channels.

Vagal nerve stimulation is widely used therapeutically but the fiber groups activated are often unknown. Aim: To establish a simple protocol to define stimulus thresholds for vagal A, B and C fibers. Methods:The intact left or right cervical vagus was stimulated with 0.1 ms pulses in spontaneously breathing anesthetized rats. Heart and respiratory rate responses to vagal stimulation were recorded. The vagus was subsequently cut distally, and mass action potentials to the same stimuli were recorded. Results: Stimulating at either 50 Hz for 2 s or 2 Hz for 10 s at experimentally determined strengths revealed A, B and C fiber thresholds that were related to respiratory and heart rate changes. Conclusion: Our simple protocol discriminates vagal A, B and C fiber thresholds in vivo.