Evoked potentials in artificial neural nets

A neural net model of discrete populations of formal neurons have been constructed to study evoked potentials based on our previous simulation studies (Anninos, 1972). Some interesting results came up from the examination of our findings regarding the latencies and the period of the cyclic activity of the evoked potentials. In fact, the different successive latencies for the five identical stimuli and the different periods for each of the cyclic activities, all are consequences of inhibitory and excitatory influences from a large neuronal population. Furthermore, such behavior of the system is not only related to the unknown neuronal population but was also substantially altered by what occurred in other systems at the time of stimulus, or prior to it.Computation assistance was provided by the Health Sciences Computing Facility, UCLA, sponsored by NIH Special Research Resources Grant RR-3. Research was sponsored by NSF Grant GB 30498 and NIH Grant NS-8498.     

Assessment of ether anesthesia in normal and spinal cats using gas--liquid chromatographic analysis of blood

A new gas-liquid chromatographic method was developed for the determination of diethylether in whole blood. Ether was quantitated by peak area ratio analysis with n-propanol as the internal standard using a flame ionization detector. Blood ether concentrations were determined in cats undergoing inhalational anesthesia by ether in oxygen. In normal spontaneously breathing cats, anesthesia began at ether concentrations of about 0.6 g/l, and respiratory arrest occurred at 2.4 g/l and above. Mean arterial blood pressure was well maintained throughout the entire anesthetic range. In spinal artificially respired animals, mean arterial blood pressure correlated inversely with blood ether concentration. The data suggest that decline in blood pressure may be a useful sign of ether toxicity in spinal cats.     

Activated lymphocytes trigger lymphoblast extravasation.

Intraperitoneal stimulation of adoptively sensitized rats with bacterial antigen promotes the localization of lymphoblasts at the site of antigen deposition. Lymphoblast extravasation activity (LEA) is generated only when specifically immune donor lymphocytes and the recipients of these cells share at least on Ag-B haplotype. However, if the specificity criteria for its formation are satisfied, LEA promotes the local development of lymphoblasts of all available specificities and irrespective of their Ag-B genotype. Allogeneic lymphoblasts do not participate actively in the delayed inflammatory reaction even when they are passively recruited into exudates. The results suggest that LEA is a T cell-derived mediator that amplifies the delayed type hypersensitivity reaction by directing recently activated lymphocytes into lesions.