Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.4.16.2 (PCP)
 3,761 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1. In electrophysiological experiments in spinalized, alpha-chloralose anaesthetized rats, opioids and anaesthetics were tested intravenously (i.v.) on the responses of individual motoneurones to alternating noxious (heat or pinch) and non-noxious (tap or vibration) stimuli. 2. On cells that were sensitive to low doses of mu-opioids, both fentanyl (0.5-4 micrograms kg-1 i.v.) and morphine (0.5 mg kg-1 i.v.) selectivity reduced reflexes to noxious stimuli to a greater degree than the higher doses required to reduce nociceptive reflexes (fentanyl 8 micrograms kg-1 i.v.; morphine 1-8 mg kg-1 i.v.) depressed non-nociceptive reflexes to a similar degree. 3. A similar spectrum of selectivity was seen with U-50,488 (0.5-16 mg kg-1 i.v.) although statistically significant selective depression of reflexes was only evident at the lowest dose tested (0.5 mg kg-1 i.v.). All effects of U-50,488 were readily reversed by low doses of the opioid antagonist, naloxone (10-100 micrograms kg-1 i.v.). 4. The dissociative anaesthetic/PCP ligand ketamine (0.5-4 mg kg-1 i.v.) was similar in having selective actions at low doses on sensitive cells but non-selective actions when higher doses were required. In contrast, the general anaesthetics methohexitone (4 mg kg-1 i.v.) and alphadolone/alphaxalone (1 mg kg-1 i.v.) were consistently non-selective between reflexes to noxious and non-noxious stimuli. alpha-Chloralose (20-40 mg kg-1 i.v.) had very little effect on reflexes to any of the synaptic inputs tested.
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PMID:On the selectivity of intravenous mu- and kappa-opioids between nociceptive and non-nociceptive reflexes in the spinalized rat. 255 13

The involvement of NMDA-type glutamate receptors in caffeine's locomotor stimulant effects and the development of tolerance to these effects was examined in rats. Caffeine and the noncompetitive NMDA receptor antagonists, MK-801 and phencyclidine (PCP), were examined alone and in combination. Caffeine produced a biphasic dose-effect curve. Both MK-801 and PCP increased locomotor activity at the highest doses tested. MK-801 and PCP shifted the caffeine curve upward, but only with the highest doses that increased locomotor activity when given alone. For the tolerance experiment, osmotic pumps containing either MK-801 or nothing at all and were implanted in rats that were given either caffeinated or drug-free tap water to drink. All rats drinking caffeine showed tolerance to its locomotor stimulant effects, whereas rats drinking drug-free tap water did not. Chronic infusion of MK-801 (0.1 and 0.3 mg/kg/day) failed to block the development of tolerance to caffeine. The 0.3 mg/kg/day infusion of MK-801 appeared to slightly delay the development of tolerance to caffeine, but this effect was probably due to the locomotor stimulant effects of this infused dose of MK-801 alone. These data provide no evidence that NMDA-type glutamate receptors play a crucial role in mediating caffeine's locomotor stimulant effects or tolerance to these effects.
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PMID:Lack of NMDA receptor involvement in caffeine-induced locomotor stimulation and tolerance in rats. 947 92

Simultaneous dispersive liquid-liquid microextraction (DLLME) and derivatization combined with gas chromatography-electron-capture detection (GC-ECD) was used to determine chlorophenols (CPs) in water sample. In this derivatization/extraction method, 500 microL acetone (disperser solvent) containing 10.0 microL chlorobenzene (extraction solvent) and 50 microL acetic anhydride (derivatization reagent) was rapidly injected by syringe in 5.00 mL aqueous sample containing CPs (analytes) and K(2)CO(3) (0.5%, w/v). Within a few seconds the analytes derivatized and extracted at the same time. After centrifugation, 0.50 microL of sedimented phase containing enriched analytes was determined by GC-ECD. Some effective parameters on derivatization and extraction, such as extraction and disperser solvent type and their volume, amount of derivatization reagent, derivatization and extraction time, salt addition and amount of K(2)CO(3) were studied and optimized. Under the optimum conditions, enrichment factors and recoveries are in the range of 287-906 and 28.7-90.6%, respectively. The calibration graphs are linear in the range of 0.02-400 microg L(-1) and limit of detections (LODs) are in the range of 0.010-2.0 microg L(-1). The relative standard deviations (RSDs, for 200 microg L(-1) of MCPs, 100 microg L(-1) of DCPs, 4.00 microg L(-1) of TCPs, 2.00 microg L(-1) of TeCPs and PCP in water) with and without using internal standard are in the range of 0.6-4.7% (n=7) and 1.7-7.1% (n=7), respectively. The relative recoveries of well, tap and river water samples which have been spiked with different levels of CPs are 91.6-104.7, 80.8-117.9 and 83.3-101.3%, respectively. The obtained results show that simultaneous DLLME and derivatization combined with GC-ECD is a fast simple method for the determination of CPs in water samples.
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PMID:Determination of chlorophenols in water samples using simultaneous dispersive liquid-liquid microextraction and derivatization followed by gas chromatography-electron-capture detection. 1751 36

The solid-phase extraction (SPE) joined with the dispersive liquid-liquid microextraction (DLLME) has been developed as an ultra preconcentration technique for the determination of chlorophenols in water samples. Chlorophenols (CPs) were employed as model compounds to assess the extraction procedure and were determined by gas chromatography-electron-capture detection (GC-ECD). In solid-phase extraction-dispersive liquid-liquid microextraction (SPE-DLLME), CPs were adsorbed from a large volume of aqueous samples (100 mL) into 100 mg functionalized styrene-divinylbenzene polymer (PPL) sorbent. After the elution of the desired compounds from the sorbent by using acetone, DLLME technique was performed on the obtained solution. Some important extraction parameters, such as sample solution flow rate, breakthrough volume, sample pH, type and volume of the elution solvent as well as the salt addition, were studied and optimized. The new method (SPE-DLLME) provided an ultra enrichment factor (4390-17,870) for 19 CPs. The calibration graphs were linear in the range of 0.001-20 microg L(-1) and the limits of detection (LODs) ranged from 0.0005 to 0.1 microg L(-1). The relative standard deviations (RSDs, for 10.0 microg L(-1) of MCPs, 5.00 microg L(-1) of DCPs, 0.200 microg L(-1) of TCPs, 0.100 microg L(-1) of TeCPs and PCP) with and without the internal standard varied from 1.1 to 6.4% (n=7) and 2.5-9.7% (n=7), respectively. The relative recoveries of the well, tap and river water samples, spiked with different levels of CPs, were 71-110%, 73-115% and 88-121%, respectively.
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PMID:Solid-phase extraction combined with dispersive liquid-liquid microextraction-ultra preconcentration of chlorophenols in aqueous samples. 1790 May 97