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Query: EC:3.1.1.7 (acetylcholinesterase)
 28,390 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The observed equilibrium constant (Kobs) for the reaction of choline acetyltransferase (EC 2.3.1.6) has been determined under physiological conditions. Using sigma and square brackets to indicate total concentrations of all ionic species present: (see article). The value of Kobs has been determined to be 12.3 plus or minus 0.6 at 38 degrees, pH 7.0 and ionic strength 0.25 M. The value at 25 degrees is not significantly different, and the constant has been found to be insensitive to variations in ionic strength (0.03 to 0.375 M), pH (6.5 TO 7.5) OR FREE [Mg-2+] (0 to 5 mM). The Kobs of this reaction reflects the difference between the observed standard free energy change (delta G-oobs) for the hydrolysis of acetylcholine and the delta G-oobs for the hydrolysis of acetyl-CoA. Since the delta G-oobs for the hydrolysis of acetyl-CoA has been previously determined to be minus 8.54 kcal/mol (minus 35.75 kJ/mol under the same physiological conditions, the delta G-oobs for the reaction of acetylcholinesterase (EC 3.1.1.7): (SEE ARTICLE). Can be calculated to be minus 6.99 kcal/mol (minus 29.26 kJ/mol) at pH ionic strength 0.25 M and 38 degrees, taking the standard state of liquid water to have unit activity ([H2O] equals 1). The pKa for acetic acid under the same conditions, has been determined to be 4.60 plus or minus 0.01, allowing the Kobs for the pH-independent reaction (see article). To be calculated to be 3.28 times 10-2 M. Choline and carnitine are chemical analogues. The Kobs for the corresponding reaction of carnitine acetyltransferase (EC 2.3.1.7). (SEE ARTICLE). Under the same physiological conditions of pH (7.0), ionic strength (0.25 M), and temperature (38 degrees) has been determined to be 1.73 plus or minus 0.05, making the delta G-oobs for the hydrolysis of acetylcholine only 1.21 kcal/mol (5.06 kJ) less negative than that for the hydrolysis of acetylcarnitine.
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PMID:Equilibrium constants of the reactions of choline acetyltransferase, carnitine acetyltransferase, and acetylcholinesterase under physiological conditions. 23

(2-Benzoylethyl)trimethylammonium chloride (BETA), a keto analog of acetylcholine, was synthesized and studied as an inhibitor of human placental choline acetyltransferase (ChA). It is a potent inhibitor of ChA with an 150 of 3.1 X 10(-6) M. The inhibition was rapid in onset and was slowly reversible. Upon dialysis of the inhibited ChA, 50% activity was recovered within about 4.90 hours. BETA was noncompetitive with respect to both substrates of ChA, acetyl-CoA and choline. BETA was selective for inhibiting ChA. It was about 100, and 50, times more potent for inhibiting ChA than acetylcholinesterase, and cholinesterase, respectively. Its activities at muscarinic and nicotinic receptors were negligible at the concentrations where complete inhibition of ChA was obtained. In contrast to the other ChA inhibitors, the styrylpyridines and halogenoacetylcholines, BETA is stable in solution. On prolonged storage (several days at 37 degrees C and pH 7.4), solutions of BETA decomposed partially into trimethylamine and vinylphenylketone. Beta was considerably more stable and more selective than other inhibitors of ChA.
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PMID:(2-Benzoylethyl)trimethylammonium chloride: a new, selective and stable inhibitor of human placental choline acetyl transferase. 30 58

A dynamic analysis of acetylcholine (ACh) level during nervous signal transmission was performed by means of computer simulation. The rate equation expressed in a system of non-linear ordinary differential equations represents the dynamic aspects of the fundamental metabolic processes in the chemical transmission at the synapse in terms of the relevant metabolite fluxes and the reactions of choline acetyltransferase, ACh receptor and acetylcholinesterase functioning in two putative homogeneous and open compartments. After a transmitter release, the ACh level in the presynaptic terminal cannot be restored by supplying the substrates of acetyl-CoA (AcCoA) and choline (Ch) at constant influx rates for ACh synthesis. A simple regulatory mechanism of linear feedback of the ACh level for variation of the substrate influx rates can accomplish the desired replenishment of ACh, in which the influx rate of AcCoA characterizes the response speed and its ratio to that of Ch governs the maintenance of the ACh level. The CoA level is ineffective for this regulatory mechanism.
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PMID:Linear feedback control of acetylcholine level in the presynaptic terminal. 196 56

In order to identify non-invasive, biochemical indicators of di(2-ethylhexyl)phthalate (DEHP) exposure, we have compared the effects in blood serum with biochemical effects in liver in rats fed a diet containing 0, 0.25, 0.75 and 2% DEHP for 2 weeks. After 3 days of treatment serum arylesterase activity levels and serum triglycerides were decreased to 60% and 20% of control values, respectively. After a 2-week treatment with DEHP the effects were generally stronger. Compared to a control group, serum arylesterase activity levels, serum triglycerides and serum cholesterol were decreased to 40%, 20% and 50%, respectively. Serum cholinesterase activity levels and serum albumin concentrations were increased by the DEHP treatment to 290% and 135% of control values, respectively. In the livers a hepatomegaly, an induction of cytochrome P-450 IVA1 and induction of the activity of palmitoyl-CoA oxidase and carnitine acetyl-CoA transferase was found to be 180%, 1080%, 1300% and 1700% of control values, respectively. The liver is a more sensitive target for DEHP exposure compared to the biochemical effects in serum, but determination of the serum parameters can be used to determine early biological effects of exposure to DEHP.
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PMID:Effect of di(2-ethylhexyl)phthalate on enzyme activity levels in liver and serum of rats. 227 65

Choline acetyltransferase (Acetyl-CoA:choline O-acetyltransferase, EC 2.3.1.6, abbreviated ChAT), the biosynthetic enzyme for acetylcholine and acetylcholinesterase (EC 3.1.1.7, abbreviated AChE) are expressed in a human cholinergic neuroblastoma cell line, MC-IXC. We have shown that ChAT activity can be regulated in culture by retinoic acid, an active metabolite of vitamin A, and by sodium butyrate, an organic fatty acid. Optimal concentrations of these agents produce 4.3-fold and 1.6-fold increases in ChAT activity, respectively. The effects of retinoic acid are statistically significant after 24 h, whereas for sodium butyrate significant differences are seen only after 48 h. Since retinoic acid stimulation of ChAT activity was reversed only by trypsin treatment and not by removal of retinoic acid from the medium, this suggests that this agent may be acting at the level of the cell surface. Other differentiating conditions, such as culture in serum-free medium or addition of 1-2% dimethylsulfoxide did not increase ChAT activity. Acetylcholinesterase activity was shown to increase only in the presence of sodium butyrate, suggesting that retinoic acid and sodium butyrate may be acting via different pathways. Retinoic acid and sodium butyrate both seem to be permissive rather than instructive in regulating ChAT activity in that they are unable to induce ChAT expression de novo in cell lines which do not already express ChAT activity.
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PMID:Stimulation of choline acetyltransferase activity by retinoic acid and sodium butyrate in a cultured human neuroblastoma. 292 23

The proposed system of continuous monitoring of enzyme activities is based primarily on the electrochemical behaviour of thiol compounds, and the experimental equipment is extremely simple. The determination of cholinesterase (EC 3.1.1.8) activity is described. The normal values obtained for men (73.9, s +/- 10.3 microkat/l) and for women (71.1, s +/- 10.2 microkat/l), lie within the usual range of analogous photometric methods. Systems for determination of the activities of alkaline phosphatase (EC 3.1.3.1) and adenosylhomocysteinase (EC 3.3.1.1) are described. The activity of aspartate aminotransferase (EC 2.6.1.1) is determined by a combination of enzyme reactions, in which CoA is released from acetyl-CoA. Analogous procedures are discussed for determinations of alanine aminotransferase (EC 2.6.1.2), lactate dehydrogenase (EC 1.1.1.27), lipase (EC 3.1.1.2), and phospholipase A2 (EC 3.1.1.4) activities, and for determination of substrates, e.g., acetate and carnitine. Possible determinations of an additional 199 enzyme activities and of some of substrates are suggested. By determining electrochemically active groups other than thiols this method becomes almost universally applicable.
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PMID:New system of continuous monitoring of enzyme activities and determination of some substrates. 344 Aug 58

Choline acetyltransferase (ChAT, acetyl-CoA-choline-O-acetyltransferase, EC 2.3.1.6) activity was measured in homogenates prepared from wild type (Canton S) and two temperature-sensitive presumed ChAT structural gene mutants (Chats1 and Chats2; originally described by Greenspan, R. (1980) J. Comp. Physiol. 137: 83-92) of Drosophila melanogaster. Wild type flies grown at 32 degrees C for 12 or 24 hr showed increased ChAT activity, whereas Chats1 and Chats2 flies showed a progressive decrease in enzyme activity at 32 degrees C (restrictive temperature) when compared to flies reared at 18 degrees C (permissive temperature). Acetylcholine (ACh) and choline levels were determined in formic acid-acetone extracts of individual fly heads, and the ACh levels showed the same variation with time at 32 degrees C as did the ChAT activity. In contrast, choline levels did not vary in any regular pattern. Acetylcholinesterase (EC 3.1.1.7) activity did not vary during heat treatment (except for Chatts2 flies held at 32 degrees C for 24 hr, where a decrease was observed) indicating that this treatment may be specific for ChAT. We conclude that ChAT activity is strongly correlated with ACh levels in Drosophila heads and may thus have an important regulatory role in determining the levels of ACh available for physiological function. We also report on the preliminary characterization of ChAT in both Chats mutants and compare the biochemical properties to those of wild type enzyme. Isoelectric focusing profiles of ChAT from both Chats mutants revealed enzymes with altered patterns compared to wild type, indicating that the mutations are most probably in the structural gene.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Choline acetyltransferase and acetylcholine levels in Drosophila melanogaster: a study using two temperature-sensitive mutants. 392 Mar 60

1. The methods for the assay of choline acetyltransferase were based on the reaction between labelled acetyl-CoA and unlabelled choline to give labelled acetylcholine. 2. Both synthetic acetyl-CoA and acetyl-CoA formed from sodium [1-(14)C]acetate or sodium [(3)H]acetate by incubation with CoA, ATP, Mg(2+) and extract from acetone-dried pigeon liver were used. 3. [1-(14)C]Acetylcholine was isolated by extraction with ketonic sodium tetraphenylboron. 4. [(3)H]Acetylcholine was precipitated with sodium tetraphenylboron to remove a ketone-soluble contaminant in sodium [(3)H]acetate and then extracted with ketonic sodium tetraphenylboron. 5. The values of choline acetyltransferase activity obtained in the presence of sodium cyanide or EDTA and synthetic acetyl-CoA were similar to those obtained with acetyl-CoA synthesized in situ. 6. The assay of acetylcholinesterase was based on the formation of labelled acetate from labelled acetylcholine. The labelled acetylcholine could be quantitatively removed from the acetate by extraction with ketonic sodium tetraphenylboron. 7. The methods were tested with samples from central and peripheral nervous tissues and purified enzymes. 8. The blank values for choline acetyltransferase and acetylcholinesterase corresponded to the activities in 20ng. and 5ng. of brain tissue respectively.
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PMID:Radiochemical micro assays for the determination of choline acetyltransferase and acetylcholinesterase activities. 498 85

1. Unilateral lesions were made in the fimbria of adult rats with a stereotaxically-applied, radio-frequency current. After 3-23 days survival, fresh, unfixed, transverse sections were cut of the forebrain. Half the sections were stained histochemically to show the distribution of acetylcholinesterase (AChE) activity. From the other sections, small, anatomically defined areas were dissected out and assayed for choline acetylase (ChAc) activity (acetyl-CoA: choline-O-acetyltransferase EC2.3.1.6).2. In the fimbria, anterior to the lesion, ChAc activity rises sharply and is still approximately twice the normal after 7 days. In the hippocampus, ChAc activity falls: in most experiments activity on the operated side was 20-40% of that on the control side, but in some experiments values below 10% were obtained. These changes closely parallel those observed in the staining for AChE.3. The results go far towards proving that the hippocampus receives a massive cholinergic innervation via the fimbria. The fibres concerned appear to be those which stain characteristically for AChE and it seems likely that other pathways showing the same histochemical behaviour are also cholinergic.
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PMID:Confirmation from choline acetylase analyses of a massive cholinergic innervation to the rat hippocampus. 605 Jun 20

Neurons in the rat central nervous system (CNS) were examined for their content of both the acetylcholine-synthesizing enzyme, choline acetyltransferase (ChAT; acetyl-CoA, choline O-acetyl-transferase, EC 2.3.16), and the transmitter-degrading enzyme, acetylcholinesterase (AChE). ChAT was localized immunohistochemically and AChE was localized histochemically in normal, colchicine-treated, or diisopropylfluorophosphate (DFP)-treated rats, either in neighboring sections by standard procedures or simultaneously in the same sections by immunofluorescence for ChAT, followed by photography, followed by histochemistry for AChE, followed by brightfield rephotography of the same neurons. This combination of fluorescence and brightfield procedures allows both to be carried out at maximum intensity without fear of interference and enables the unambiguous visualization of all neurons that might be expected with either procedure. Based on previous examination of singly stained neighboring sections, five CNS areas were examined in detail in DFP-treated rats using the simultaneous procedure for localizing both ChAT and AChE in the same neurons in the same sections. Several hundred neurons were thus examined in each area. These areas were the caudate putamen, nucleus basalis of Meynert, medial septum, nucleus of the diagonal band of Broca (vertical and horizontal limbs), and zona incerta. In the caudate putamen and nucleus basalis magnocellularis of Meynert, all ChAT-positive neurons contained AChE and vice versa. In the medial septum and nucleus of the diagonal band of Broca, all ChAT-positive neurons contained AChE, but these neurons containing both ChAT and AChE were intermingled with neurons positive only for AChE.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Identification of central cholinergic neurons containing both choline acetyltransferase and acetylcholinesterase and of central neurons containing only acetylcholinesterase. 635 2


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