PubMed Health⌕ Search

Biomedical subjects

R M Ridley

Publications and source records attributed to R M Ridley.

146 records · Page 9Linked to original sources

Variable expression in the functional psychoses. A comparison with Huntington's disease.

The variability in presentation and the interaction between age of onset, symptomatology and the calculation of penetrance in Huntington's disease is used as a framework within which to consider whether the various presentations of the functional psychoses could be different manifestations of the effects of a single gene. The phenomenon of the biotype, i.e., the tendency for family members to resemble each other in symptomatology in a manner which is too variable within families to be explained by either genetic or allelic heterogeneity but which is too stable within families to be explained by random variation, is clearly demonstrable in Huntington's disease. In families with multiple cases of psychosis, the tendency for the diagnosis in the proband to prevail in other affected individuals together with the possible occurrence in yet other individuals of different diagnostic categories at above chance levels may also be an example of the biotype phenomenon. While genetic heterogeneity in the functional psychoses probably also occurs, the possible variation in expression of single genes predicts that the correspondence between different genes and diagnostic subtypes would be limited.

Bipolar Disorder↗

Survival of nigral grafts within the striatum of marmosets with 6-OHDA lesions depends critically on donor embryo age.

The study examined the importance of embryonic donor age for the survival of nigral grafts in 6-OHDA-lesioned marmosets. The issue as to whether donor age is critical for the survival of nigral grafts in primates is controversial, because several early reports suggested that relatively old tissue could survive transplantation and produce functional benefits in monkeys, in contrast to the restrictive time dependence observed in rodents. Embryonic marmoset donors embryos of three different ages were employed: 1) E74 (Carnegie stage 18-19); 2) E83-84 (Carnegie stage 23+); 3) E92-93 (foetal period). The nigral neurons derived from the ventral mesencephalon in the two older donor age groups did not survive well when grafted to the striatum of adult marmosets with unilateral 6-OHDA lesions. Although a few tyrosine hydroxylase (TH+) neurons could be identified by immunohistochemistry at graft sites in all recipients in older donor age groups, the numbers of surviving neurons in these were small, on average typically less than 100 TH+ cells. These small grafts were not sufficient to affect amphetamine-induced rotation. In contrast, many more TH+ cells typically survived transplantation in the recipients of graft tissue derived from the youngest donors and amphetamine-induced rotation was significantly reduced in this group alone. The time course and extent of the reduction in rotation was remarkably similar to that observed in previous marmoset nigral graft studies, confirming the utility of amphetamine-induced rotation as a sensitive and reliable indicator of nigral graft function in this species. Considering these results and other recent evidence from monkey to monkey, human to rat, and human to human graft studies, the survival of embryonic nigral tissues derived from primate donors transplanted into the striatum does appear to be critically dependent on the age of the donor tissue.

Animals↗