Stimulation increases incorporation of [3H]lysine into rat brain and liver proteins.

Exposure of rats to electric footshocks or merely to the footshock apparatus increased the incorporation of [3H]lysine into brain and liver protein. The effect was present in both fore-and hindbrain. The footshock treatment was the more effective stimulus, producing larger and more significant changes. These results resemble those previously observed in C57Bl/6J mice, and thus suggest that altered protein or amino acid metabolism is a general response to stress in rodents.

Effects of handling and etherization on incorporation of [3H] lysine into protein of mouse brain and liver.

A standardized handling experience of 20 sec duration elevated the amount of radioactive lysine incorporated into brain total proteins during a 10 min labeling period begun either 10 min or 30 min after the handling. Etherization for 20 sec produced similar metabolic changes. Incorporation of [3H] lysine into liver proteins was minimally affected by handling, while slightly altered by etherization. The metabolic changes detected in the brain after handling did not appear to be side-effects of changes in blood-borne radioactivity. The results indicate that laboratory stresses often thought to be of minor importance can have large effects on ordinary assays of protein metabolism in brain.

Effect of sensory stimulation on the uptake and incorporation of radioactive lysine into protein of mouse brain and liver.

Alterations in incorporation of tritiated lysine into protein of mouse brain and liver were observed following brief exposure to a variety of sensory stimuli. During a 15-min session, subjects were trained to perform a one-way active avoidance response or else were exposed to one of the stimulus components of the situation, including shocks, buzzers, lights, handling, and the apparatus alone. Twenty min after these behavioral treatments, tritiated lysine was injected subcutaneously, and its incorporation into total protein during a 10-min pulse was measured. Quiet mice, undisturbed until injection of the precursor, constituted the baseline group for biochemical comparisons. Most behavioral treatments increased the total amount of radioactivity in brain and liver. The treatments increased the incorporation of radioactivity into protein of both organs even more, thereby producing elevations of relative radioactivity (RR) of protein, a measure of the amount of radioactivity incorporated into protein relative to that in the acid-soluble pools. The RR increases following most of the behavioral experiences were approximately equal; however, exposure to lights or to the apparatus were less effective than the other treatments in eliciting these metabolic changes. The responses were greatly diminished in mice previously exposed to the treatments. Thus, the effectiveness of a stimulus in producing these metabolic alterations may depend upon its apparent magnitude and its novelty. The total radioactivity increases were larger in brain than in liver, while the RR increases were smaller in brain than in liver. Brain RR increases were of equal magnitude when the precursor was injected 5, 20, or 35 min after behavioral treatment, whereas the liver RR responses declined markedly over this period. Despite these differences, strong positive correlations between brain and liver across the various behavioral treatments existed. The RR changes occurred about equally in the cerebellum-brain stem, basal ganglia, hippocampus-septum, and ventral cortex, while the thalamus-hypothalamus and dorsal cortex showed smaller differences.