Literature DB >> 16125866

Minor disturbances in central nervous system function in familial neurohypophysial diabetes insipidus.

J Bruins1, G L Kovács, A P Abbes, J P H Burbach, E L T van den Akker, H Engel, A A M Franken, D de Wied.   

Abstract

Familial neurohypophysial diabetes insipidus (FNDI) is caused by a defect in vasopressin synthesis and release as a result of a heterozygous mutation in the gene for the vasopressin prohormone. The predominant characteristic of FNDI is excessive thirst and urine production. However, vasopressin not only has peripheral endocrine effects, but also regulates numerous brain functions. We investigated whether central functions are affected in FNDI, by studying neuropsychological functioning of 23 affected members (15 males, 8 females) of a large family carrying a T/G transition mutation at nucleotide 2110 (codon 116) of the vasopressin prohormone gene (Cys116Gly). The relatively large number of family members with FNDI made it possible to compare cognitive and other CNS effects in these subjects with those of family members without FNDI. Thirty-seven adult volunteers (20 males, 17 females) from the same family and 11 non-family members (2 males, 9 females) from northern part of The Netherlands were tested. The mean age of the subjects was 35+/-12 years. Of the 63 quantified neuropsychological parameters few were statistically different between the subjects with FDNI and control subjects. Memory retrieval processes and sustained attention were worse in the subjects with FDNI. Moreover, these individuals reported significantly fewer symptoms of agoraphobia and miscellaneous symptoms, and had significantly lower scores on a scale measuring anger. The performance of FNDI subjects on an auditory verbal learning test (the 15-word test learning trial) was worse, but not significantly so, than that of the subjects without FDNI. There were subjective complaints of forgetfulness and slow recalls and those were observed in daily life by non-affected family members. These moderate differences in neuropsychological performance indicate that in human FNDI parvocellular vasopressin systems that supply the brain may be less affected or give no such serious disabilities, than the magnocellular hypothalamo-neurohypophysial system that provides vasopressin for endocrine regulation of water homeostasis.

Entities:  

Mesh:

Year:  2005        PMID: 16125866     DOI: 10.1016/j.psyneuen.2005.06.001

Source DB:  PubMed          Journal:  Psychoneuroendocrinology        ISSN: 0306-4530            Impact factor:   4.905


  4 in total

Review 1.  The challenge of translation in social neuroscience: a review of oxytocin, vasopressin, and affiliative behavior.

Authors:  Thomas R Insel
Journal:  Neuron       Date:  2010-03-25       Impact factor: 17.173

2.  Impact of sleep, neuroendocrine, and executive function on health-related quality of life in young people with craniopharyngioma.

Authors:  Kristin A Niel; Kimberly L Klages; Thomas E Merchant; Merrill S Wise; Donna Hancock; Mary Caples; Belinda N Mandrell; Heather M Conklin; Valerie Mclaughlin Crabtree
Journal:  Dev Med Child Neurol       Date:  2021-03-22       Impact factor: 4.864

3.  Viral rescue of magnocellular vasopressin cells in adolescent Brattleboro rats ameliorates diabetes insipidus, but not the hypoaroused phenotype.

Authors:  K C Schatz; L M Brown; A R Barrett; L C Roth; V Grinevich; M J Paul
Journal:  Sci Rep       Date:  2019-06-03       Impact factor: 4.379

4.  A hypomorphic vasopressin allele prevents anxiety-related behavior.

Authors:  Mirjam Bunck; Ludwig Czibere; Charlotte Horvath; Cornelia Graf; Elisabeth Frank; Melanie S Kessler; Chris Murgatroyd; Bertram Müller-Myhsok; Mariya Gonik; Peter Weber; Benno Pütz; Patrik Muigg; Markus Panhuysen; Nicolas Singewald; Thomas Bettecken; Jan M Deussing; Florian Holsboer; Dietmar Spengler; Rainer Landgraf
Journal:  PLoS One       Date:  2009-04-09       Impact factor: 3.240

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.