Regional brain variations of cytochrome oxidase activity in spontaneously hypertensive mice.

To explore the central disturbances resulting from blood pressure changes, spontaneously hypertensive mice (SHM) were compared to normotensive controls for cytochrome oxidase (CO) activity, an index of oxidative capacity in the central nervous system and a marker of long-term regional brain metabolism and neuronal activity. In all brain areas presenting significant enzymatic variations, only increases in CO activity were found in SHM, particularly the central autonomic network. However, only specific regions were affected, namely the insular cortex and the hypothalamic nuclei principally involved in high-order autonomic control. Altered limbic structures included the lateral septum, various hippocampal subregions, as well as prelimbic cortex. CO activity was also elevated in several forebrain regions, including those directly connected to the limbic system, such as the nucleus accumbens, the claustrum, and dorsomedial and reticular thalamic nuclei, as well as subthalamic and ventrolateral thalamic nuclei. In the brainstem, the only regions affected were the locus coeruleus, site of noradrenergic cell bodies, the trigeminal system, and four interconnected regions: the inferior colliculus, the paramedial reticular formation, the medial vestibular, and the cerebellar fastigial nuclei. These data show that specific regions modulating sympathetic nerve discharge are activated in young adult SHM, possibly due to mitochondrial dysfunction and excitotoxicity.

Comparisons between C57BL/6J and A/J mice in motor activity and coordination, hole-poking, and spatial learning.

The C57BL/6J (B6) inbred mouse strain was compared to the A/J inbred strain for motor activity in an open-field, exploration of a hole-board, motor coordination in the coat-hanger test, and spatial learning in the Morris water maze. B6 mice displayed a higher number of segment crossings in the open-field and of hole-poking responses than A/J mice. The performance of B6 mice was superior to that of A/J mice not only in the submerged but also in the visible platform version of the Morris water maze. By contrast to their hypoactivity, the A/J strain had shorter movement times in the coat-hanger test, indicating faster motor speed, although the groups did not differ in latencies before falling. These results indicate that recombinant inbred or congenic strains derived from B6 and A/J mice offer considerable potential for discerning the genetic basis of several behavioral phenotypes.

Longitudinal analysis of motor activity and coordination, anxiety, and spatial learning in mice with altered blood pressure.

Mice with either high or low blood pressure (BP) were compared to normotensive controls at 2 and 12 months of age for motor activity, equilibrium, anxiety, and spatial learning. Irrespective of age, high BP mice were more active in an open field than normotensive controls, whereas low BP mice were hypoactive at 2 months of age. High BP mice had a higher number of entries and a longer duration of visits in the open arms, a higher open arm/total arm ratio, a longer duration for the first visit into an open arm, and lower latencies before entering the first open arm than controls in the elevated +-maze, indicative of reduced anxiety. Reduced levels of anxiety were also displayed by low BP mice for the duration of the first open arm visit (both age groups) and for the time spent in the open arms (older group). In the motor coordination test (coat-hanger), high BP mice had higher two-paw movement time and reached the top of the apparatus on fewer occasions than controls. Both groups with abnormal BP values were deficient during visuomotor guidance in the water maze. These results indicate strain-, age-, and test-specific abnormalities in mice with uncontrolled hypertension or hypotension.

Effects of bilateral electrolytic lesions of the medial nucleus accumbens on exploration and spatial learning.

Rats with electrolytic lesions of the medial part of the nucleus accumbens, comprising the shell region, were compared to sham-operated rats in tests of exploration in a T-maze, in a hole-board, and in an elevated (+)-maze and in a test of water maze spatial learning. Rats with medial nucleus accumbens lesions had higher choice latencies than sham-operated controls during the beginning of the spontaneous alternation test. A higher number of hole pokes was found in the lesioned group, but only during the beginning of the second day of testing. In the elevated (+)-maze, lesioned rats had a higher number of closed and total arm entries and spent more time in the center region. The lesioned group did not differ from the control group for the number of alternations in the T-maze, for horizontal and vertical motor activity in the hole-board, and for acquisition or reversal of spatial learning in the Morris water maze. These results indicate that lesions of the medial nucleus accumbens slowed down decision time during spontaneous alternation testing and increased exploration in a time and test-specific manner without altering acquisition of a reference memory task.

Beam sensorimotor learning and habituation to motor activity in lurcher mutant mice.

Lurcher mutant mice lose cerebellar granule cells and Purkinje cells. The mutants were compared to normal mice in a beam-walking task. Normal mice were placed on a slippery bridge while lurchers, because of their severe ataxia, were placed on a bridge with the same diameter, but enveloped with surgical tape to improve traction. The performance of both groups improved with repeated trials. In an activity box, lurcher mutants were as active as normal mice, showed normal intrasession habituation, and emerged from a toy object as easily as normal mice. These results indicate that the cerebellar damage in lurchers does not prevent the acquisition of a motor skill task requiring balance in an immobile apparatus. Ataxia was not accompanied by hypoactivity, inhibition or disturbances in intrasession habituation.

Climbing sensorimotor skills in Lurcher mutant mice.

Lurcher mutant mice, characterized by massive degeneration of cerebellar granule and Purkinje cells, were compared to normal mice of the same background strain in three sensorimotor learning tasks requiring climbing skills. In the coat-hanger test, Lurcher mutants were deficient in forepaw contact time and four paw latencies. Improvement over time was weak for both groups. For latencies before reaching the halfway point or the top of the diagonal bar in the same apparatus, Lurcher mutants showed gradual improvement while normal mice appeared to lose motivation to perform the task. In a rope-climbing test, a slight reduction in movement time was detected in Lurcher mutants with repeated trials, whereas the performance of normal mice was stable over time. In a water escape pole-climbing test, Lurcher mutants were impaired relative to controls. Both groups decreased the time required before grasping the pole across days of testing. The number of segments climbed was increased in Lurcher mutants across days. These results illustrate that massive cerebellar damage does not eliminate the possibility of acquiring climbing skills, but under some conditions limit performance.

Absence of an association between motor coordination and spatial orientation in lurcher mutant mice.

Lurcher mutant mice were impaired in spatial orientation and motor coordination in comparison to normal mice. Both groups improved across days in both invisible and visible water maze platform conditions. Contrary to normal mice, lurcher mutants did not improve over days in terms of the time taken to reach a side-bar in a motor coordination test, an indication of defective motor learning. However, lurchers were able to stay on the bar longer across days. These results indicate that motor learning deficits in this cerebellar-damaged animal are not absolute but dependent on the type of measurement attempted. There was no correlation between motor coordination and spatial orientation for normal mice. A similar absence of correlation was noted for lurcher mutants, except for falling latencies in the coat-hanger test during the middle of training.