The cholinergic system in the cerebellum: from structure to function

The cerebellar cholinergic system belongs to the third type of afferent nerve fiber system (after the climbing and mossy fibers), and has important modulatory effects on cerebellar circuits and cerebellar-mediated functions. In this report, we review the cerebellar cholinergic system, including cholinergic origins and innervations, acetylcholine receptor expression and distributions, cholinergic modulations of neuronal firing and synaptic plasticity, the cholinergic role in cerebellar-mediated integral functions, and cholinergic changes during development and aging. Because some motor and mental disorders, such as cerebellar ataxia and autism, are accompanied with cerebellar cholinergic disorders, we also discuss the correlations between cerebellar cholinergic dysfunctions and these disorders. The cerebellar cholinergic input plays an important role in the modulation of cerebellar functions; therefore, cholinergic abnormalities could induce physiological dysfunctions.

Neural Photoreception in a Lamellibranch Mollusc

The pallial nerves of Spisula solidissima each contain a single afferent nerve fiber which responds directly to illumination of the nerve, and apparently mediates the "shadow" response of siphon retraction. These units show constant-frequency spontaneous activity in the dark; illumination abruptly inhibits this discharge, and cessation of the light stimulus then evokes a prolonged burst of impulses at high frequency (the off-response). Impulses are initiated at a point near the visceral ganglion, and propagated unidirectionally toward it. Stimulation with monochromatic light has revealed that more than one photoreceptor pigment is involved, since the discharge patterns evoked are wavelength-specific. Inhibition is relatively prominent at short wavelengths, excitation at long wavelengths. Following selective adaptation with blue light, "on" responses can be produced with red stimuli, demonstrating the unmasking of an excitatory event which takes place during illumination. The two photoreceptor pigments may be segregated in two or more cells presynaptic to the recorded unit, or,—more likely—may both be contained in the same cell. The spectral sensitivity function for inhibition shows a single maximum at 540 mµ, and is probably dependent upon a carotenoid pigment. No photoreceptor function has been demonstrated for a hemoprotein, apparently identical with cytochrome h, which occurs in high concentration in Spisula nerve.