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  • 1980-1984  (5)
  • 1
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: An ontogenetic survey of the basic protein of myelin, common to both central and peripheral nervous systems, was carried out on normal C57B1 and five dysmyelinating mutant mice. Myelin basic protein (MBP) was quantified by radioimmunoassay in the optic and sciatic nerves of mice from birth to adult stages, giving special attention to the premyelinating and early myeli-nation periods. In the optic nerves of normal mice, MBP was already detectable at birth but the active period of myelin deposition was shown to occur after day 10 postnatal. The timing and rate of accumulation of MBP were normal in Trembler. In contrast, they were abnormal in the other mutants. In the quaking mouse, the active period of MBP deposition was delayed, and its final concentration represented no more than 12% of normal in the adult. No active period of MBP deposition was observed in the other mutants. In the jimpy mouse, a slow accumulation of MBP resulted in a final concentration reaching 2% of the normal value at 25 days. In mid and shiverer mice, the MBP was hardly detectable. In the sciatic nerves of normal mice, the active period of MBP deposition occurred between days 3 and 12 postnatal. No substantial changes occurred in the period of 2 months-2 years. Deposition of MBP was normal in jimpy. In quaking, it was not only delayed but also reduced, leading to a concentration as low as 40% of normal adult. In mid and shiverer PNS, MBP concentrations were very low but noticeably higher than in the optic nerve. In the sciatic nerve of Trembler a myelination-demyelination process was strongly suggested by MBP determination. After a delayed but active period of deposition from days 5–11 postnatal, the MBP content was found to decline within a few days and remained almost undetectable until old age.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The particulate material of aquaeous homogenate of forebrain was separated by zonal centrifugation in a continuous 0.4-1.2 m-sucrose gradient after sedimentation at 100,000 g to eliminate the soluble material. Based on the absorbance at 280 nm, four major peaks were obtained from adult normal mice corresponding to 1.1 m (A), 0.68 m (B), 0.35 m (C), and 0.12 m (D) sucrose. The two smaller and lighter peaks, C and D, were not present when purified myelin was separated by the same procedure. B consisted of pure compact myelin; A was made of vesicles, sometimes with a double membrane. Throughout development, the myelin peak shifted from 0.58 m in young animals to 0.70 m in very old ones. Moreover, the myelin peak B drastically increased during development, as compared with peak A.-In the Trembler, the profile was close to normal, with a slightly higher yield of myelin which also peaked at a higher density. In the quaking, there were only two shoulders in the myelin density range at 0.68 m and 0.75 m; in the Jimpy only a faint shoulder was seen, at approximatively 0.67 m. In the shiverer, B was absent and only an A peak was present, at approximatively 0.85-0.90 m, which contained non-compact lamellar membranes and myelin figures with an abnormal major dense line. In the mid (an allele of shiverer) the density profile resembled the one obtained in the shiverer (one peak in the 0.88 m region). When considering myelin basic protein (MBP) content in the normal developing animal, it was minimum in fraction A, mainly found in the B myelin peak, but also present in the light fraction (C + D). In young animals this latter peak was prominent, in contrast to the adult. In the Trembler mutant, the profile was close to normal; in the quaking, MBP was mainly found in peak A (0.85 m), and in the Jimpy MBP was very low and nearly constant throughout the gradient (with faint quantities in light C + D fraction). In mid, the content was very low, with a peak in the 0.88 m region, in contrast with its shiverer allele, where MBP is hardly detected. More meaningful myelin studies can be carried out by using zonal centrifugation in continuous sucrose gradient, to determine the density of mutant myelin and the degree of myelin maturation in animals.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Intrauterine growth retardation (IUGR) induced by ligation of one uterine artery on day 17 of pregnancy in the rat lead to major abnormalities in the fatty acid content of neurons and oligodendrocytes but not in astrocytes. In neurons from IUGR rats, monounsaturated fatty acids were decreased; in the polyunsaturated series, ω-3 fatty acids were increased and Ω-6 fatty acids were decreased. In oligodendrocytes, monounsaturated fatty acids were also decreased, but the modifications in polyunsaturated fatty acids were the opposite of those in neurons: Ω-3 being decreased and w-6 increased. Although the animals received a normal diet after birth, the alterations were still present in adulthood. In addition, fatty acid composition of brain cells is a very indicative criterion of brain maturation.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 42 (1984), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Total polyribosomes were isolated from the brains of 16–20-day C57BL/6 mice, four neurological mutants (qk/qk, shi/shi, mld/mld, and jp/Y), and four heterozygote or littermate controls (qk/+, shi/+, mld, and jp littermates) and translated in a homologous, cell-free system. No differences were observed among the nine genotypes in either the yield of polysomes (32.2 ± 0.6 A260/g brain) or in the incorporation of [35S]methionine into trichloroacetic acid-precipitable protein. However, when the four myelin basic proteins (BPs) were isolated from the translation mixtures little incorporation of [35S]methionine into the BPs was noted in those assays directed by polysomes from mld/mld or from shi/shi animals. Compared with C57BL/6 polysomes, mld littermate and shi/+ polysomes incorporated approximately half the levels of label into the four BPs while qk/+ and qk/qk incorporated normal and close-to-normal levels. Polysomes from jp littermates and jp/Y brains synthesized 66% and 〈 15% of the levels of the 14K BP compared with C57BL/6 polysomes. Incorporation of label into the other three BPs was normal with jp littermate polysomes and about half the control levels with jp/Y polysomes. The data indicate that shi/shi and mld/mld mutants either produce altered BPs not recognized by our antibody or synthesize very low levels of BP. The data provide additional support for the notion that the qk/qk mutant synthesizes much higher levels of MBP than are incorporated into myelin. They also indicate that in the jimpy mutant the synthesis of the four BPs is affected to differing extents; thus, the mutant cannot be easily characterized as either an “assembly” or “synthesis” defect.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 320 (1982), S. 26-33 
    ISSN: 1432-1912
    Keywords: Convulsions ; Noradrenaline release ; Cerebral cortex ; Brain stem ; MOPEG levels ; Quaking mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The Quaking mouse is a genetically determined model of convulsive disorders. We investigated the modulation of noradrenergic neurotransmission through α2-adrenoceptors in the occipital cortex and the brain stem of this mutant. The endogenous levels of noradrenaline were similar in the cerebral cortex of the Quaking mice and their corresponding controls, while a significant increase of endogenous noradrenaline was found in the brain stem of the mutants. The rate of disappearance of noradrenaline in the cerebral cortex and the brain stem after injection of FLA 63 was identical in control and Quaking mice. The calciumdependent electrically evoked overflow of 3H-noradrenaline from slices of occipital cortex was inhibited by clonidine and enhanced by yohimbine in Quaking as well as in normal mice. The negative feed-back mechanism mediated by presynaptic α2-adrenoceptors operates to a similar extent in both strains of mice. In contrast to the occipital cortex, in the brain stem, the amount of neurotransmitter released by electrical stimulation was significantly increased in Quaking mice when compared with the controls. However, in the brain stem, the negative feed-back regulation of noradrenaline release operates to a similar extent in both strains of mice. When the endogenous levels of MOPEG were determined in the brain stem, they were found to be significantly higher in the Quaking mice when compared to the controls. The results suggest that an increase in noradrenergic neurotransmission in the brain stem, rather than in the cerebral cortex, could contribute to the behavioural abnormalities exhibited by the Quaking mice.
    Type of Medium: Electronic Resource
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