Increased branching of basal dendrites on pyramidal neurons in the occipital cortex of homozygous Brattleboro rats in standard and enriched environmental conditions: A Golgi study

Abstract As a continuation of our previous reports in a series of studies on the brain of Brattleboro rats, the branching of basal dendrites of pyramidal neurons in the upper layers of the occipital cortex was quantified in three groups of male heterozygous and homozygous Brattleboro rats. One group raised in standard environmental conditions was killed at 60 days of age, and another from standard conditions was killed at 90 days of age. A third group from enriched environmental conditions was killed at 90 days of age after 30 days of enrichment. Comparing the two types of Brattleboro rats, the homozygous rats showed significantly more total dendritic branching segments per neuron in both the 60-day-old standard condition group and the 90-day-old enriched group. A similar measure (segments per primary branch) was also significantly greater in homozygous than in heterozygous rats at 60 days of age. In the 90-day-old enriched group, the homozygous rats showed a trend toward more segments per primary branch than the heterozygous rats. The results suggest that the complete absence of vasopressin produces metabolic effects which, at certain ages or in certain environmental conditions, increase the branching of basal dendrites of pyramidal neurons in the upper layers of the occipital cortex.

[1]  P. Hoffman,et al.  Proposed mechanisms of action of neurohypophyseal peptides in memory processes and possible routes for the biosynthesis of peptides with a C-terminal carboxamide group. , 1977, Advances in biochemical psychopharmacology.

[2]  F. Volkmar,et al.  Effects of rearing complexity on dendritic branching in frontolateral and temporal cortex of the rat. , 1973, Experimental neurology.

[3]  F. Volkmar,et al.  Pattern of dendritic branching in occipital cortex of rats reared in complex environments. , 1973, Experimental neurology.

[4]  M C Diamond,et al.  ENVIRONMENTAL ENRICHMENT IN BRATTLEBORO RATS: BRAIN MORPHOLOGY , 1982, Annals of the New York Academy of Sciences.

[5]  T. W. Greidanus,et al.  Behavioral and endocrine responses of rats with hereditary hypothalamic diabetes insipidus (Brattleboro strain) , 1975, Physiology & Behavior.

[6]  W. Krieg Connections of the cerebral cortex. I. The albino rat. A. Topography of the cortical areas , 1946 .

[7]  R. Buijs,et al.  The distribution of vasopressin and oxytocin in the rat brain , 1978, Neuroscience Letters.

[8]  Masatoshi Tanaka,et al.  Catecholamine concentration and turnover in discrete regions of the brain of the homozygous Brattleboro rat deficient in vasopressin. , 1978, Endocrinology.

[9]  M. Diamond,et al.  Increase in thickness of cerebral cortex in response to environmental enrichment in brattleboro rats deficient in vasopressin , 1981, Experimental Neurology.

[10]  T. Powell,et al.  The basic uniformity in structure of the neocortex. , 1980, Brain : a journal of neurology.

[11]  E. Bennett,et al.  Effects of differential experience on neuronal nuclear and perikarya dimensions in the rat cerebral cortex. , 1975, Behavioral biology.

[12]  K. Kuypers,et al.  Effects of differential environments on plasticity of dendrites of cortical pyramidal neurons in adult rats , 1978, Experimental Neurology.

[13]  H. Valtin Hereditary hypothalamic diabetes insipidus in rats (Brattleboro strain). A useful experimental model. , 1967, The American journal of medicine.

[14]  D. Wied,et al.  Memory deficit in rats with hereditary diabetes insipidus , 1975, Brain Research.

[15]  C. P. Leblond,et al.  Response of the three main types of glial cells of cortex nad corpus callosum in rats handled during suckling or exposed to enriched, control and impoverished environments following weaning , 1977, The Journal of comparative neurology.

[16]  M. Tanaka,et al.  Arginine8-vasopressin affects catecholamine metabolism in specific brain nuclei. , 1977, Life sciences.

[17]  A. Moses,et al.  Accumulation and release of pituitary vasopressin in rats heterozygous for hypothalamic diabetes insipidus. , 1970, Endocrinology.

[18]  M. Diamond Anatomical Brain Changes Induced by Environment , 1976 .

[19]  W. Greenough,et al.  Environmental complexity modulates growth of granule cell dendrites in developing but not adult hippocampus of rats , 1978, Experimental Neurology.

[20]  Uylings Hb,et al.  Ordering methods in quantitative analysis of branching structures of dendritic trees. , 1975 .

[21]  M. Diamond,et al.  Effect of age and enrichment on certain brain dimensions in Brattleboro rats deficient in vasopressin , 1982, Experimental Neurology.

[22]  D. Wied,et al.  Inferior quality of RSA during paradoxical sleep in rats with hereditary diabetes insipidus , 1975, Brain Research.

[23]  J. Pettigrew,et al.  Restoration of visual cortical plasticity by local microperfusion of norepinephrine , 1979, The Journal of comparative neurology.

[24]  Edward L. Bennett,et al.  Chemical and Anatomical Plasticity of Brain: Replications and Extensions, 1970 , 1972 .

[25]  G. Kovacs,et al.  The interaction of posterior pituitary neuropeptides with monoaminergic neurotransmission: significance in learning and memory processes. , 1980, Progress in brain research.