Manganese is absorbed mainly via ingestion, but can also be inhaled. It binds to alpha-2-macroglobulin, albumin, or transferrin in the plasma and is distributed to the brain and all other mammalian tissues, though it tends to accumulate more in the liver, pancreas, and kidney. Manganese is capable of existing in a number of oxidation states and is believed to undergo changes in oxidation state within the body. Manganese oxidation state can influence tissue toxicokinetic behavior, and possibly toxicity. Manganese is excreted primarily in the faeces. (L228)
Manganese is a cellular toxicant that can impair transport systems, enzyme activities, and receptor functions. It primarily targets the central nervous system, particularily the globus pallidus of the basal ganglia. It is believed that the manganese ion, Mn(II), enhances the autoxidation or turnover of various intracellular catecholamines, leading to increased production of free radicals, reactive oxygen species, and other cytotoxic metabolites, along with a depletion of cellular antioxidant defense mechanisms, leading to oxidative damage and selective destruction of dopaminergic neurons. In addition to dopamine, manganese is thought to perturbations other neurotransmitters, such as GABA and glutamate. In order to produce oxidative damage, manganese must first overwhelm the antioxidant enzyme manganese superoxide dismutase. The neurotoxicity of Mn(II) has also been linked to its ability to substitute for Ca(II) under physiological conditions. It can enter mitochondria via the calcium uniporter and inhibit mitochondrial oxidative phosphorylation. It may also inhibit the efflux of Ca(II), which can result in a loss of mitochondrial membrane integrity. Mn(II) has been shown to inhibit mitochondrial aconitase activity to a significant level, altering amino acid metabolism and cellular iron homeostasis. (L228)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
致癌物分类
对人类无致癌性(未列入国际癌症研究机构IARC清单)。
No indication of carcinogenicity to humans (not listed by IARC).
Manganese mainly affects the nervous system and may cause behavioral changes and other nervous system effects, which include movements that may become slow and clumsy. This combination of symptoms when sufficiently severe is referred to as
Manganese mainly affects the nervous system and may cause behavioral changes and other nervous system effects, which include movements that may become slow and clumsy. This combination of symptoms when sufficiently severe is referred to as
The subcellular distribution of The subcellular distribution of manganese in brains of mice chronically administered manganese in different chemical forms with food was examined using gel chromatography. Male ddY-mice were divided into five groups of six animals each, and Groups 1 to 4 were given 2 g/kg manganese of standard laboratory mouse chow) in the form of manganese chloride, manganese acetate, manganese carbonate, or manganese oxide, in the diets for 12 months, while Group 5 served as control. Twenty four hours after the last feed, animals were decapitated and brains were rapidly removed for study of the different regions (corpus striatum, hypothalamus, midbrain, cerebral cortex, hippocampus, cerebellum, and medulla oblongata). Subcellular fractions (mitochondrial, microsomal and cytosolic) and gel chromatography fractions were analyzed for manganese contents using flame atomizer absorption spectrophotometry. Results showed that cerebral cortex levels of manganese in mice exposed to the nearly insoluble manganese carbonate and manganese oxide were higher than in controls, while manganese concentrations in the corpus striatum were similar to those in controls. Microsomal manganese in treated mice was also higher than in controls. The gel chromatographic profile of corpus striatum showed that 20% manganese was in the high molecular weight fractions, 45% was in the middle molecular weight fractions, while 32% was in the low molecular weight fractions. The percent manganese in high molecular weight fractions was higher (29% to 49%) in the manganese treated groups, than in controls. The percentage of manganese in low molecular weight fractions of the manganese oxide exposed group (9%) was lower than in the manganese chloride, manganese acetate, and manganese carbonate exposed groups (42%, 36%, and 38%, respectively).
Process for preparing transition metal cyclopentadienyl carbonyl
申请人:Ethyl Corporation
公开号:US05026885A1
公开(公告)日:1991-06-25
Transition metal cyclopentadienyl carbonyl compounds of the formula: [R.sub.x C.sub.p M(CO).sub.y ].sub.n wherein R is hydrocarbyl, C.sub.p is cyclopentadienyl, M is a transition metal, x is 0 or an integer from 1 to 5, y is an interger from 1 to 7, provided that when x is 2 to 5, R can represent two or more different hydrocarbyl groups and any two R groups can together form a fused ring with the cyclopentadienyl moiety, and n is 1 or 2, are prepared in one step by carbonylating a mixture of (i) a transition metal salt of an organic carboxylic acid a .beta.-diketone, or a .beta.-keto ester (ii) a cyclopentadiene compound (iii) and a metal alkyl reducing agent.
Additives and lubricant formulations for improved antioxidant properties
申请人:Esche K. Carl
公开号:US20060205615A1
公开(公告)日:2006-09-14
A method and compositions for lubricating surfaces with lubricating oils exhibiting increased antioxidant properties. The lubricated surface includes a lubricant composition containing a base oil of lubricating viscosity and an amount of at least one hydrocarbon soluble metal compound effective to provide a reduction in oxidation of the lubricant composition greater than a reduction in oxidation of the lubricant composition devoid of the hydrocarbon soluble metal compound. The metal of the metal compound is selected from the group consisting of titanium, zirconium, and manganese.
Metal complexes of the formula 1 [L.sub.n M.sub.m X.sub.p ].sup.z Y.sub.q (1) where M is manganese in oxidation state II, III, IV, V and/or VI or cobalt in oxidation state II and/or III or iron in oxidation state II and/or III, X is a coordinating or bridging group, Y is a counterion in the appropriate stoichiometric amount to compensate an existing charge z, where z as the charge of the metal complex can be positive, zero or negative, n and m independently of one another are integers from 1 to 4, p is an integer from 0 to 15, q is z/charge of Y, and L is a ligand of the formula (2), (3) or (4) ##STR1## and A and R.sup.1 to R.sup.8 are as defined in the description.
COMPOSITE OF METAL OXIDE NANOPARTICLES AND CARBON, METHOD OF PRODUCTION THEREOF, ELECTRODE AND ELECTROCHEMICAL ELEMENT EMPLOYING SAID COMPOSITE
申请人:Naoi Katsuhiko
公开号:US20130095384A1
公开(公告)日:2013-04-18
A composite powder in which highly dispersed metal oxide nanoparticle precursors are supported on carbon is rapidly heated under nitrogen atmosphere, crystallization of metal oxide is allowed to progress, and highly dispersed metal oxide nanoparticles are supported by carbon. The metal oxide nanoparticle precursors and carbon nanoparticles supporting said precursors are prepared by a mechanochemical reaction that applies sheer stress and centrifugal force to a reactant in a rotating reactor. The rapid heating treatment in said nitrogen atmosphere is desirably heating to 400° C.-1000° C. By further crushing the heated composite, its aggregation is eliminated and the dispersity of metal oxide nanoparticles is made more uniform. Examples of a metal oxide that can be used are manganese oxide, lithium iron phosphate, and lithium titanate. Carbons that can be used are carbon nanofiber and Ketjen Black.
Composite of metal oxide nanoparticles and carbon, method of production thereof, electrode and electrochemical element employing said composite
申请人:Naoi Katsuhiko
公开号:US09287553B2
公开(公告)日:2016-03-15
A composite powder in which highly dispersed metal oxide nanoparticle precursors are supported on carbon is rapidly heated under nitrogen atmosphere, crystallization of metal oxide is allowed to progress, and highly dispersed metal oxide nanoparticles are supported by carbon. The metal oxide nanoparticle precursors and carbon nanoparticles supporting said precursors are prepared by a mechanochemical reaction that applies sheer stress and centrifugal force to a reactant in a rotating reactor. The rapid heating treatment in said nitrogen atmosphere is desirably heating to 400° C.-1000° C. By further crushing the heated composite, its aggregation is eliminated and the dispersity of metal oxide nanoparticles is made more uniform. Examples of a metal oxide that can be used are manganese oxide, lithium iron phosphate, and lithium titanate. Carbons that can be used are carbon nanofiber and Ketjen Black.