Faculty Bibliography

With the Vibratome modification of the Falck-Hillarp technique, and with the indirect immunofluorescence technique for visualizing the first three enzymes in catecholamine synthesis, evidence has been obtained that in the rat olfactory bulb several periglomerular cells are dopaminergic. Both tyrosine hydroxylase and dopadecarboxylase, converting tyrosine to DOPA and DOPA to dopamine (DA), respectively, but not dopamine-beta-hydroxylase, converting DA to noradrenaline, are present in periglomerular cell bodies, as well as in their intraglomerular dendrites. These findings suggest that DA may be active at dendrodentritic synapses known to be present between periglomerular and mitral and/or tufted cells.

1. The activity of single units was recorded from the striate cortex (area 17) of anaesthetized, paralysed cats. Responses to stimuli moving at different velocities were examined. 2. Peak evoked firing frequency, rather than fotal evoked spikes, is used throughout as a measure of response. The former mea-ure gives curves of response vs. velocity that correlate well with curves of contrast sensitivity vs. velocity, wheras the latter does not. 3. Cortical receptive fields were classified according to the criteria of Hubel & Wiesel. Simple cells were found to prefer lower velocities (mean 2-2 deg sec-1) than complex cells( mean 18-8 deg sec-1). The response of simple cells to stimuli moving faster than 20 deg sec-1 is generally poor; complex cells usually discharge briskly to these speeds. 4. Cells classified as hypercomplex by the end-inhibition criterion were further chara-terized as type I or type II, according to the suggestion of Dreher (1972). Type I units are indistinguishable from simple cells in their velocity tuning, and type II units equally clearly resemble complex cells. These results are therefor consistent with Dreher's sbudivision. 5. Teh selectivity of cells for velocity is variable but can be quite marked. The average selectivities of simple and complex cells are not significantly different. There is an inverse correlation between preferred velocity and the sharpness of velocity selectivity for simple cells; no trend is apparent for other cell types. 6. No clear correlation is observed between the velocity preferances of units and their degree of direction selectivity, or receptive field arrangement. Simple cells with 'sustainef' temporal responses to flashed stimuli tend to prefer slower rates of movement than 'transient' ones, and to be less selective for velocity. 7. The results for different cortical cell-types are compared with the velocity tuning of X- and Y-cells in the lateral geniculate nucleus

We studied the influence of Mn, La, and D600 on action potentials and plateau currents in cardiac Purkinje fibers. The Ca antagonists each abolished the second inward current, but they failed to act selectively. Voltage clamp experiments revealed two additional effects: decrease of slow outward current (iotachi) activation, and increase of net outward time-independent plateau current. These effects occurred at inhibitor concentrations used in earlier studies, and were essential to the reconstruction of observed Ca antagonist effects on electrical activity. The inhibitory influence of Mn, La, and D600 on iotachi suggested that iotachi activation might depend upon prior Ca entry. This hypothesis was not supported, however, when [Ca]omicron was varied: elevating [Ca]omicron enhanced Ca entry, but iotachi was nevertheless depressed. Thus, the results suggested instead that Ca antagonists and Ca ions have rather similar effects on iotachi, possibly mediated by changes in membrane surface charge

Acetylcholinesterase (AChE) has been localized in the rabbit cornea by light and electron microscopy histochemical techniques. In the stroma, the enzyme is concentrated in nerves. In the epithelium, the enzyme is concentrated in intercellular spaces devoid of nerves. The morphologic appearance of the enzyme staining by light and electron microscopy in the epithelium is similar; consequently, the staining demonstrated with light microscopy examination does not always represent epithelial nerves. A significant portion of corneal acetylcholinesterase therefore appears unrelated to nerves. Considerably smaller deposits of enzyme reaction product were present in cells in every layer of the cornea, using electron microscopy histochemistry; they were not identified by light microscopy