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Epinephrine, effect

Kidney decreases glomerular filtration rate Lung, intestine, genital system inhibited Metabolic effects, weak epinephrine effect... [Pg.788]

When monkeys have low serotonin levels, they become aggressive. This response is thought to be a model for violence against oneself or family members, possibly related to a failure to counteract epinephrine effects. High aggressiveness in monkeys was correlated with low levels of metabolic products of serotonin in spinal fluid. In humans, low levels of serotonin metabolites in spinal fluid also correlate with the severity of physical aggression. [Pg.4]

Chemicals known as beta blockers are sometimes used to counteract epinephrine effects in patients suffering from heart disease as discussed in Section 15.11. [Pg.437]

Izgi C, Cevik C, Nugent K. Severe myocardial ischemia after concentrated epinephrine use for the treatment of anaphylaxis Kounis syndrome or epinephrine effect Heart Lung 2010 39(2) 160-3. [Pg.249]

Epinephrine is also known as adrenaline and is a hormone with profound physiological effects designed to prepare the body for fight or flight... [Pg.688]

Catecholamines. The catecholamines, epinephrine (EPl adrenaline) (85), norepinephrine (NE noradrenaline) (86) (see Epinephrine and norepinephrine), and dopamine (DA) (2), are produced from tyrosine by the sequential formation of L-dopa, DA, NE, and finally EPl. EPl and NE produce their physiological effects via CC- and -adrenoceptors, a-Adrenoceptors can be further divided into CC - and a2-subtypes which in turn are divided... [Pg.533]

Desflurane is less potent than the other fluorinated anesthetics having MAC values of 5.7 to 8.9% in animals (76,85), and 6% to 7.25% in surgical patients. The respiratory effects are similar to isoflurane. Heart rate is somewhat increased and blood pressure decreased with increasing concentrations. Cardiac output remains fairly stable. Desflurane does not sensitize the myocardium to epinephrine relative to isoflurane (86). EEG effects are similar to isoflurane and muscle relaxation is satisfactory (87). Desflurane is not metabolized to any significant extent (88,89) as levels of fluoride ion in the semm and urine are not increased even after prolonged exposure. Desflurane appears to offer advantages over sevoflurane and other inhaled anesthetics because of its limited solubiHty in blood and other tissues. It is the least metabolized of current agents. [Pg.409]

The modern usage of P2" go Asts for the treatment of asthma dates to 1903 when the effect of injected epinephrine [51-43-4] (adrenaline) C2H23NO2, (1 R = CH3) was investigated (see Epinephrine and norepinephrine) (33). As in some other modem treatments, eg, xanthines and anticholinergics, the roots of P2" go Ast therapy for asthma can be found in historical records which document the use of herbal extracts containing ephedrine [299-42-3] C qH NO, (2) as bronchodilators. Epinephrine and ephedrine are stmcturaHy related to the catecholamine norepinephrine [51-41-2] CgH NO, (1, R = H), a neurotransmitter of the adrenergic nervous system (see Neuroregulators). [Pg.438]

Because of the widespread nature of adrenoceptors, nonselective P-agonists can produce many undesirable side effects. Therefore, before adrenergic agonists could become widely used in the treatment of asthma, some selectivity in action was needed. Whereas epinephrine and ephedrine have significant agonist activity at both a and P adrenoceptors, isoproterenol is a selective agonist at the P receptor (39). However, isoproterenol does not distinguish between the P and receptors and it is not active orally. [Pg.439]

These agents are often combined with a vasoconstrictant such as epinephrine [51-43-4]. By using such a combination, the local anesthetic is held in the area for a longer period of time and its effect extended hemorrhage is minimized, blood loss prevented, and a better surgical repair obtained. [Pg.405]

Removal of one of the aromatic hydroxyl groups gives an agent similar to epinephrine in its effects but with longer dura-... [Pg.63]

Adrenergic blocking agent. A drug that blocks the effects of epinephrine and/or norepinephrine. [Pg.448]


See other pages where Epinephrine, effect is mentioned: [Pg.109]    [Pg.344]    [Pg.587]    [Pg.175]    [Pg.61]    [Pg.170]    [Pg.605]    [Pg.352]    [Pg.109]    [Pg.344]    [Pg.587]    [Pg.175]    [Pg.61]    [Pg.170]    [Pg.605]    [Pg.352]    [Pg.342]    [Pg.408]    [Pg.464]    [Pg.68]    [Pg.180]    [Pg.129]    [Pg.55]    [Pg.370]    [Pg.824]    [Pg.561]    [Pg.761]    [Pg.62]    [Pg.63]    [Pg.65]    [Pg.95]    [Pg.241]    [Pg.20]    [Pg.19]    [Pg.140]    [Pg.382]    [Pg.193]   


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