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Caffeine targets

When a nerve impulse reaches the synaptic knob the neurotransmitter is ejected into the synaptic cleft and serves as a stimulus to the next adjacent neuron. The vast majority of all impulses transmitted occur at the synaptic gaps, although recent research indicates that chemical transmission can occur at other points along the axon. Many neurological diseases and psychiatric disorders result from a disturbance or alteration of synaptic activity. Drugs such as tranquilizers, anesthetics, nicotine, and caffeine target the synapse and can cause an alteration of impulse transmission. [Pg.526]

Beyond Viagra, there are a number of other PDE inhibitors that are used clinically. In fact, the classic drugs papaverine and dipyridamole were used clinically before their effects on PDEs were known. Caffeine and theophylline (a compound found in tea) are also PDE inhibitors. However, all of these drugs most likely have multiple targets, making conclusions regarding the roles of PDEs in processes that are sensitive to these agents difficult to interpret. Certainly, some of their effects are due to their actions on adenosine receptors. [Pg.965]

Affinity of MIP towards the target analyte should be examined prior to fabrication of the chemosensor. Batch binding assays are used to test selectivity of suitable MIPs. Especially, affinity of MIP to compounds, which are structurally related to the target analyte, should be tested. If MIP binds similarly with these compounds as the template, then cross-reactivity is manifested [156], This effect was exploited for determination of adenine and its derivatives with the use of MIP templated with 9-ethyladenine. Nevertheless, the cross-reactivity, if undesired, can be avoided by suitable sample pretreatment, e.g. by interferant extraction with a supported liquid membrane (SLM) coupled to the MIP-PZ chemosensor. The Fluoropore membrane filter of submicrometre porosity can serve that purpose. That way, this membrane holds interferants, thus eliminating the matrix effect. The SLM-involving determination procedure is cheaper than traditional laborious sample pretreatment used to remove the interfering substances. For instance, caffeine [143] and vanillin [157] in food samples have been determined using this procedure. [Pg.228]

Teenagers are the target of many beverage makers who produce drinks that carry an extra caffeine kick. [Pg.45]

In the study described the time-dependence and reversibility of the enzyme induction was not studied. Also the enzyme substrate used as a marker for the CYP 1A2 activity was caffeine, which although frequently encountered in the target population and commonly used as a marker for CYP 1A2 activity, is not a drug with a narrow therapeutic index used by the target population. The enzyme substrate used as a marker for the CYP 3A4 activity, urinary 6- 3-hydroxy-cortisol and free cortisol, although readily amenable to inclusion in studies, is not a drug and is also known to be a relatively insensitive marker for CYP 3A4 induction. Also urinary 6- 3-hydroxy-cortisol and free cortisol does not differentiate between intestinal and liver CYP 3A4 activities. [Pg.685]

As can be seen from Table I a substantial number of alkaloids display significant insect toxicity, including nicotine, pipeline, lupine alkaloids, caffeine, gramine, strychnine, berberine, ephedrine, and steroidal alkaloids. Only the specialists can tolerate the respective alkaloids. The tobacco homworm (Manduca sexto), for example, can grow on a diet with more than 1% nicotine without any adverse effects. Most of the nicotine is either degraded or directly eliminated via the Malpighian tubules and in feces 182). Because nicotine binds to the acetylcholine (ACH) receptor, it is likely that in Manduca this receptor has been modified in such a way that ACH can still bind, but not nicotine (so-called target site modification). [Pg.22]

Purine receptors Adenosine, AMP, ADP and ATP can act extracellularly as hormones or transmitters, too In particular, adenosine receptors that occur in the heart, the brain, and the lung are the targets of theophylline and caffeine. Adenosine itself is being used for the treatment of a special type of cardiac arrhythmia. [Pg.68]

Adenosine receptors are targeted by drags such as theophylline and caffeine. [Pg.75]

The toxic concentrations for theophylline in neonates have not been well defined, and can vary from infant to infant. Other pharmacokinetic factors, such as low plasma protein binding and limited capacity for excretion could make neonates prone to aminophylline toxicity. Fetuses and neonates can develop theophylline toxicity even with plasma concentrations in the target range, since they can metabolize theophylline to caffeine, adding to the methyl-xanthine load. [Pg.3363]

SPME can also be used to extract target analytes from food and drug samples. Thus, it has been employed for the extraction of caffeine from coffee and tea [225], and for that of volatile impurities in drugs. Headspace SPME has also been tested for flavour analysis in foods. Thus, the SPME/GC/TOF-MS tandem was successfully used for the rapid analysis of volatile flavour compounds in apple fruit. The sample (300-450 g of apple) was subjected to static headspace sampling for 4 6 h in order to allow the volatiles... [Pg.171]


See other pages where Caffeine targets is mentioned: [Pg.345]    [Pg.109]    [Pg.420]    [Pg.14]    [Pg.263]    [Pg.266]    [Pg.267]    [Pg.282]    [Pg.45]    [Pg.213]    [Pg.229]    [Pg.102]    [Pg.325]    [Pg.227]    [Pg.439]    [Pg.540]    [Pg.177]    [Pg.418]    [Pg.446]    [Pg.74]    [Pg.408]    [Pg.423]    [Pg.59]    [Pg.397]    [Pg.165]    [Pg.189]    [Pg.119]    [Pg.525]    [Pg.721]    [Pg.706]    [Pg.151]    [Pg.155]    [Pg.258]    [Pg.345]    [Pg.86]    [Pg.183]    [Pg.185]    [Pg.39]    [Pg.77]    [Pg.326]   
See also in sourсe #XX -- [ Pg.45 ]




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