Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0040822 (tremor)
 18,428 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Folic acid (FA) and certain of its reduced congeners produce excitatory effects when applied to neuronal tissue. Recent evidence has suggested that folates have other biological properties in common with the excitatory amino acids. The purpose of this study was to determine the activity of folate compounds in a system sensitive to excitatory amino acids. Bilateral injection of folic acid into the nucleus accumbens resulted in a marked increase in locomotor activity at doses of 2.5 and 5 micrograms. Larger doses resulted in behavioral responses, such as body tremor and labored breathing, which interfered with the locomotor response. Similarly, 5-formyltetrahydrofolic acid (FTHF) produced a marked hypermotility response after bilateral injection into the nucleus accumbens (2.5-25 micrograms), while dihydrofolic acid, tetrahydrofolic acid, and 5-methyltetrahydrofolic acid were ineffective. Pretreatment with reserpine (10 mg/kg, i.p.) markedly reduced the hypermotility response elicited by folic acid and FTHF as did pretreatment with haloperidol in both peripheral (0.8 mg/kg) and direct (5 micrograms) injection into the nucleus accumbens. In addition, injection of muscimol (30 ng), which depresses hypermotility induced by dopamine and amphetamine, produced a significant decrease in the hypermotility response produced by folic acid. In contrast, pretreatment with phentolamine (5 mg/kg, i.p.) or propranolol (4 mg/kg, i.p.) did not decrease folic acid or FTHF-induced responses. These results suggest that folic acid and FTHF produce an increase in locomotor activity by facilitating dopaminergic neurotransmission in the nucleus accumbens, possibly by inducing the release of dopamine from the nerve terminals. Thus, these folates have effects similar to those of the excitatory amino acids when injected into the nucleus accumbens.
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PMID:Folate induced-hypermotility response after bilateral injection into the nucleus accumbens of the rat. Possible mediation through dopaminergic mechanisms. 302 81

Magnetic resonance imaging (MRI) has been shown to be a very effective tool for monitoring the formation and dissociation of hydrates because of the large intensity contrast between the images of the liquid components and the solid hydrate. Tetrahydrofuran/water hydrate was used because the two liquid components are miscible and form hydrate at ambient pressure. These properties made this feasibility study proceed much faster than using methane/water, which requires high pressure to form the hydrate. The formation and dissociation was monitored first in a THF/water-saturated Berea sandstone plug and second in the bulk. In both cases it appeared that nucleation was needed to begin the formation process, i.e., the presence of surfaces in the sandstone and shaking of the bulk solution. Dissociation appeared to be dominated by the rate of thermal energy transfer. The dissociation temperature of hydrate formed in the sandstone plug was not significantly different from the dissociation temperature in bulk.
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PMID:Monitoring hydrate formation and dissociation in sandstone and bulk with magnetic resonance imaging. 1468 13

Alkyl-capped silicon nanocrystals can be dispersed in aqueous media by shaking or stirring their solutions in organic solvents (DMSO, ether, THF) with excess water. THF is the most straightforward choice with which to prepare stable aqueous dispersions, because the nanocrystals are very soluble in THF and it is also miscible with water. As little as 0.01% v/v tetrahydrofuran is sufficient. DMSO and ether were the preferred choices for subsequent staining of live cells because THF shows some acute toxicity even when very dilute. The luminescence intensity of the aqueous dispersions is linear in particle concentration and independent of pH over the range 5-9. The sols retain their photoluminescence and are stable against flocculation for at least 6 months.
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PMID:Dispersions of alkyl-capped silicon nanocrystals in aqueous media: photoluminescence and ageing. 1893 35

The salt (eta(5)-pentamethylcyclopentadienyl)silicon(II) tetrakis(pentafluorophenyl)borate (5) reacts at -78 degrees C with lithium bis(trimethylsilyl)amide in dimethoxyethane (DME) as solvent to give quantitatively the compound [bis(trimethylsilyl)amino][pentamethylcyclopentadienyl]silicon(II) 6A in the form of a colorless viscous oil. The reaction performed at -40 degrees C leads to the silicon(IV) compound 7, the formal oxidative addition product of 6A with DME. Cycloaddition is observed in the reaction of 6A with 2,3-dimethylbutadiene to give the silicon(IV) compound 8. Upon attempts to crystallize 6A from organic solvents such as hexane, THF, or toluene, the deep yellow compound trans-1,2-bis[bis(trimethylsilyl)amino]-1,2-bis(pentamethylcyclopentadienyl)disilene (6B), the formal dimer of 6A, crystallizes from the colorless solution, but only after several days or even weeks. Upon attempts to dissolve the disilene 6B in the described organic solvents, a colorless solution is obtained after prolonged vigorous shaking or ultrasound treatment. From this solution, pure 6A can be recovered after solvent evaporation. This transformation process can be repeated several times. In a mass spectroscopic investigation of 6B, Si=Si bond cleavage is observed to give the molecular ion with the composition of 6A as the fragment with the highest mass. The X-ray crystal structure analysis of the disilene 6B supports a molecule with a short Si=Si bond (2.168 A) with efficiently packed, rigid sigma-bonded cyclopentadienyl substituents and silylamino groups. The conformation of the latter does not allow electron donation to the central silicon atom. Theoretical calculations at the density functional level (RI-BP86 and B3LYP, TZVP basis set) confirm the structure of 6B and reveal for silylene 6A the presence of an eta(2)-bonded cyclopentadienyl ligand and of a silylamino group in a conformation that prevents electron back-donation. Further theoretical calculations for the silicon(II) compound 6A, the disilene 6B, and the two species 11 and 11* derived from 6A (which derive from Si=Si bond cleavage) support the experimental findings. The reversible phase-dependent transformation between 6A and 6B is caused by (a) different stereoelectronic and steric effects exerted by the pentamethylcyclopentadienyl group in 6A and 6B, (b) some energy storage in the solid state structure of 6B (molecular jack in the box), (c) a small energy difference between 6A and 6B, (d) a low activation barrier for the equilibration process, and (e) the gain in entropy upon monomer formation.
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PMID:Reversible transformation of a stable monomeric silicon(II) compound into a stable disilene by phase transfer: experimental and theoretical studies of the system {[(Me3Si)2N](Me5C5)Si}n with n = 1,2. 1965 48