Neurochemical pathology最新文献

{"title":"Partial proceedings of the scientific program of the 17th annual meeting of the American Society for Neurochemistry: Neurochemical consequences of hepatic disease. Montreal, March 16-21, 1986.","authors":"","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"6 1-2","pages":"1-166"},"PeriodicalIF":0.0,"publicationDate":"1987-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14747583","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The role of astrocytes in hepatic encephalopathy.","authors":"M D Norenberg","doi":"10.1007/BF02833599","DOIUrl":"https://doi.org/10.1007/BF02833599","url":null,"abstract":"<p><p>The Alzheimer type II astrocyte change is the distinctive morphologic alteration in brain of humans and experimental animals succumbing to hepatic encephalopathy (HE). Whether this change is a primary event in the pathogenesis of HE or whether it is secondary to injury of some other component(s) of the CNS has not been clarified. Studies in a rat model of HE have revealed early reactive changes in astrocytes characterized by cytoplasmic hypertrophy. During the later phases, degenerative changes ensue corresponding to the Alzheimer type II change observed by light microscopy. In view of the role of astrocytes in ammonia detoxification and the importance of ammonia in the pathogenesis of HE, we have suggested that the initial astrocytic changes are the morphological correlates of ammonia detoxification. We have speculated that the later degenerative alterations could lead to failure by astrocytes to carry out key functions (e.g., neurotransmitter uptake, ion regulation, and the like) and contribute the development of the encephalopathy. Recently, the potential involvement of astrocytes in HE has been further investigated, using primary astrocyte cultures. Exposure of cultures to ammonia at clinically relevant concentrations has shown morphologic changes closely resembling those observed in experimental HE in vivo. These deleterious effects can partly be prevented by raising cyclic AMP levels in cells. Other potential toxins (octanoic acid, phenol) have shown pathologic changes as well. Although some alterations were common to all three, they each possessed distinctive pathological effects. A synergistic interaction has also been demonstrated with these toxins. Functional studies of ammonia-treated astrocytes have shown the following: With low doses or short-term exposure, the uptakes of K+, glutamate, and GABA remained unchanged or slightly increased, whereas with higher doses or longer treatment, those activities diminished. A fall in ATP values occurred with prolonged ammonia treatment. Preliminary findings have shown no significant derangements in the beta-adrenergic receptor, except for a slight decrease in receptor affinity. However, cyclic AMP production was diminished following stimulation with isoproterenol. A slight rise in the number of benzodiazepine receptors was found. These studies indicate that profound changes occur in astrocytes following exposure to ammonia and other putative toxins. It is proposed that toxins and factors involved in the precipitation of HE do so by affecting astroglial properties. Derangements in such properties may lead to glial dysfunction (primary gliopathy), resulting in an encephalopathic state.</p>","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"6 1-2","pages":"13-33"},"PeriodicalIF":0.0,"publicationDate":"1987-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF02833599","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14433235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Reformation of specific synaptic connections by regenerating sensory axons in the spinal cord of the bullfrog.","authors":"E Frank,&nbsp;D W Sah","doi":"10.1007/BF02842934","DOIUrl":"https://doi.org/10.1007/BF02842934","url":null,"abstract":"<p><p>The regrowth of sensory axons into the spinal cord of juvenile bullfrogs was studied after disruption of these fibers in the dorsal root. Within 9 d after the root had been frozen, regenerating sensory axons had reached the spinal cord, as revealed by labeling with horseradish peroxidase. Growth into the spinal cord, however, was much slower. Even several months after denervation, very few fibers had reestablished any of their normal longitudinal projections within the dorsal funiculus. Eventually, however, sensory axons grew across the region and into the dorsal horn. Intracellular recordings from motoneurons revealed that these axons made functional reconnections with spinal neurons. Muscle sensory axons established direct, monosynaptic inputs to motoneurons, whereas cutaneous fibers innervated these neurons polysynaptically. Moreover, sensory afferents from a particular muscle distinguished among different classes of motoneurons, just as in normal frogs. Thus, specific synaptic pathways can be reestablished by regenerating sensory axons if they can reach their appropriate target region within the spinal cord.</p>","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"5 3","pages":"165-85"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF02842934","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14620484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Presynaptic elements on artificial surfaces. A model for the study of development and regeneration of synapses.","authors":"R W Burry","doi":"10.1007/BF02842943","DOIUrl":"https://doi.org/10.1007/BF02842943","url":null,"abstract":"<p><p>Recently a model has been developed to study the synapse formation in which the components of a synapse can be isolated and examined independently. The observation of neurites forming presynaptic elements on polylysine-coated surfaces is a model for which the formation of presynaptic elements can be studied independently of a cellular postsynaptic element. Studies with neurons from both cell cultures and the intact cerebellum have shown that beads coated with poly-basic proteins can serve as a \"postsynaptic element.\" With use of this system, observation have shown that the presynaptic element can form quickly, within 3 h, and contain many of the characteristics of a mature presynaptic element, such as synaptic vesicle antigens. Additional studies have shown that astrocytes appear to be involved in the loss or removal of the presynaptic elements on beads. Thus, synaptogenesis may involve the development of inappropriate synaptic contacts, which are eliminated by astrocytes. The lack of regeneration in the central nervous system (CNS) also may involve the astrocyte's ability to remove immature and/or inappropriate presynaptic elements and growth cones as they attempt to cross the lesion site.</p>","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"5 3","pages":"345-60"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF02842943","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14433229","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Specificity of neuromuscular connections during early development and following regeneration of motor axons in the bullfrog.","authors":"P B Farel","doi":"10.1007/BF02842935","DOIUrl":"https://doi.org/10.1007/BF02842935","url":null,"abstract":"<p><p>The specificity of neuromuscular connectivity was examined in unoperated bullfrog (Rana catesbeiana) tadpoles and in tadpoles that had undergone transection of the three ventral roots that normally innervate the hindlimb. The specificity of motoneuron projections was assessed by applying small amounts of horseradish peroxidase to circumcribed hindlimb regions and mapping the locations of retrogradely labeled motoneurons within the lumbar lateral motor column (LMC). In unoperated tadpoles, the locations of retrogradely labeled motoneurons in the LMC were as circumscribed at early stages of development as in tadpoles examined after motoneuron number in the LMC had stabilized. Six to eight weeks after ventral root transection in young tadpoles, localization of retrogradely labeled motoneurons was almost as circumscribed as found in unoperated tadpoles. However, localization following regeneration became less precise in more advanced tadpoles. If the ventral roots of adult frogs were crushed rather than transected, motor axon regeneration was considerably more precise, confirming previous reports (Westerfield and Powell, 1983). The implications of these results for hypotheses of neuromuscular specificity are discussed.</p>","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"5 3","pages":"187-203"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF02842935","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14620485","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Papers from a symposium: Neural Development, Plasticity, and Regeneration. April 19-21, 1985, Columbus, OH.","authors":"","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"5 3","pages":"153-368"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14747577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Reactive synaptogenesis in the CNS. A comparison of regenerating and sprouting systems.","authors":"M Murray","doi":"10.1007/BF02842936","DOIUrl":"https://doi.org/10.1007/BF02842936","url":null,"abstract":"<p><p>Lesion-induced synaptogenesis was compared in the goldfish retinotectal system, which readily regenerates after optic nerve crush, and in the cat spinal cord, in which collateral sprouting has been demonstrated after dorsal rhizotomy. Quantitative electron microscopic methods were used. Reinnervation of the tectum was complete, but was characterized by a prolonged time course. Reinnervation appeared to be achieved by retinal axons and not by sprouting from nonretinal axons. Reinnervation in the cat spinal cord was also virtually complete, but was very rapid and may be mediated by some axons that are similar to those destroyed and by other axons that are different.</p>","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"5 3","pages":"205-20"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF02842936","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14747578","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Dorsal root axonal regeneration in the adult frog spinal cord. A model of vertebrate CNS regeneration.","authors":"F J Liuzzi,&nbsp;R J Lasek","doi":"10.1007/BF02842938","DOIUrl":"https://doi.org/10.1007/BF02842938","url":null,"abstract":"<p><p>The frog dorsal root provides a useful model for the study of axonal regeneration in an adult vertebrate CNS. We have used the model to compare the regeneration of two very different types of axons within the same CNS environment and have found that regenerating dorsal root, as well as rerouted motoneuron axons, display similar growth patterns in the spinal cord. Both sensory and motor axons grow preferentially in some regions and not in others. They both regenerate effectively longitudinally as well as radially within the dorsolateral fasciculus (DLF). By contrast, fewer sensory and motor axons regenerate longitudinally or radially in the dorsal funiculus (DF). This similar preferential growth of two very different populations of axons suggests that the growth patterns reflect regional differences in the cellular environment of the cord. The DLF has fascicles of unmyelinated axons separated by radial glial processes and, after dorsal root injury, is mildly gliotic. By contrast, DF has very large myelinated axons, which widely separate the radial glial processes that traverse the region. After dorsal root injury, this region is markedly gliotic and contains myelin, debris and oligodendroglia, and microglial macrophages. Our data suggest that unmyelinated axons and radial glial processes are more preferred substrates for axonal growth than myelin debris, oligodendroglia and macrophages. It is not surprising, then, that regions of the adult mammalian CNS that are characterized by large myelinated axons fail to support axonal growth. Moreover, there is some evidence that regions of the adult mammalian CNS that are characterized by unmyelinated axons support axonal growth.</p>","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"5 3","pages":"237-53"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF02842938","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14434082","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Structural protein transport in elongating motor axons after sciatic nerve crush. Effect of a conditioning lesion.","authors":"I G McQuarrie","doi":"10.1007/BF02842933","DOIUrl":"https://doi.org/10.1007/BF02842933","url":null,"abstract":"<p><p>In elongating motor axons of the rat sciatic nerve, the maximum outgrowth rate increased from 4.6 to 5.3 mm/d (5.3-6.1 X 10(-8) m/s) when a testing lesion of spinal nerves L4 and L5 was preceded 2 wk earlier by a conditioning lesion of the sciatic nerve. Axonal outgrowth was examined by measuring the transport of 35[S]methionine-labeled structural proteins (tubulin, actin, and neurofilament triplet) from \"parent\" axon stumps into \"daughter\" axon sprouts. Since these proteins are conveyed by the slow component of axonal transport at 1-5 mm/d (1.2-6.0 X 10(-8) m/s), the isotope was injected into the spinal cord 1 wk before the testing lesion. Nerves were removed 8 d after the testing lesion, sectioned into 3-mm segments, and homogenized; soluble proteins were separated by polyacrylamide gel electrophoresis. Fluorographs were used as templates to identify gel segments for removal, solubilization, and liquid scintillation counting. Distributions of mean radioactivity for tubulin, actin, and neurofilament triplet were plotted for animals receiving a conditioning vs sham-conditioning lesion. Greater amounts of tubulin and actin were transported into daughter axons in the conditioned group. Tubulin was mainly increased in axon shafts, whereas actin was mainly increased in axon tips. These findings suggest that the axonal transport of tubulin and actin governs the rate of elongation.</p>","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"5 3","pages":"153-64"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF02842933","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13591192","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Control of neuron shape during development and regeneration.","authors":"M J Cohen,&nbsp;G F Hall","doi":"10.1007/BF02842942","DOIUrl":"https://doi.org/10.1007/BF02842942","url":null,"abstract":"<p><p>We have examined the ability of Mueller reticulospinal neurons in the CNS of the larval sea lamprey to sprout following axonal and dendritic injury. Axotomy induces regenerative sprouting exclusively from the axon stump if it occurs at a site distant from the soma in the spinal cord. However, axotomy within the hindbrain at a site close to the soma results in profuse neuritic sprouting from the dendrites. The gross morphology and trajectories of these \"dendritic\" sprouts resemble those of regenerating axons. Amputation of Mueller cell dendrites (dendrotomy) without axotomy does not result in neuritic sprouting from either the axon or dendrites, indicating that axotomy is specifically required for sprouting to occur. However, dendrotomy is capable of altering the distribution of sprouting in a previously axotomized Mueller cell by inducing sprouting at the site of the dendrotomy lesion. Sprouts of both dendritic and axonal origin tend to follow linear, rostrocaudally oriented paths along or near the ventral surface of the hindbrain. Some sprouts form very large, palmate growth cones on the marginal surface, which in turn give rise to many branches that continue to grow either rostrally or caudally along the surface of the brain. We discuss the possibility that both dendritic and axonal sprouts evoked by axotomy of Mueller neurons are recapitulating initial axonal development during embryogenesis, and that their trajectories are determined by developmental guidance cues persisting in the ventral hindbrain.</p>","PeriodicalId":77753,"journal":{"name":"Neurochemical pathology","volume":"5 3","pages":"331-43"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF02842942","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14434086","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}