Binding sites of vasopressin (VP) have been characterized in the hippocampal synaptic plasma membranes of developing normal and hypothyroid rats using a highly specific tritiated VP antagonist, d(CH,),Tyr(Me)VP (V, type). This antagonist bound to an apparently homogeneous population of specific site
Effects of neonatal hypothyroidism on cerebral and cerebellar synaptosome development
β Scribed by M. Anthony Verity; W. J. Brown; M. Cheung; H. Huntsman; R. Smith
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 761 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0360-4012
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β¦ Synopsis
Abstract
The effect of hypothyroidism on cerebral and cerebellar synaptosome development has been studied. Neonatal hypothyroidism was induced following addition of 0.3% propylthiouracil to the diet of nursing mothers. Maturation profiles of total synaptosome fraction and specific activities of lactate dehydrogenase, Na+K ATPase, cytochrome c oxidase, and protein were obtained from days 6 to 32 on synaptosomes isolated from Ficollβsucrose gradients. The greatest changes were found in the total activities of enzymes isolated from the cerebellum. Hypothyroidism induced a retardation of LDH and cytochrome c oxidase in cerebellar synaptosomes, but no change in corresponding specific activities. Maximum rates of ^14^Cβleucine incorporation into cerebellar synaptosome protein was found at 16β20 days, after which a rapid decline occurred to adult levels at 32 days. In neonatal hypothyroidism, synthesis was significantly reduced at 8 and 14 days, but reached control levels or above at 21β32 days. In the cerebrum, maximum rates of ^14^Cβleucine incorporation into synaptosome protein were identified at 8β12 days in normal with a rapid drop to adult levels at approximately 20 days. In neonatal hypothyroidism, peak activities were identified at 14 days and increased activities over control were noted at 14, 20 and 30 days.
These observations demonstrate the sensitivity of the developing cerebellar synaptic apparatus to neonatal hypothyroidism, with a protraction in the peak levels of synaptosome protein synthesis in cerebrum and cerebellum.
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