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L-norepinephrine

L-norepinephrine and dopamine are present in some plants and act as agonists for both a- and P-adrenergic receptors [1]. Further plant P-adrenergic receptor agonists include the phenylpropanoid alkaloids L-... [Pg.531]

L-norepinephrine, In nerve cells /.-dopa is convened to dopamine then to L-norepineph-rine as follows usina two enzyme catalysts ... [Pg.123]

Certain biogenic amines, including 5-hydroxytrypt-amine (serotonin), L-norepinephrine, and P-phenyl-ethylamine, are removed from pulmonary circulation whereas others, such as histamine, dopamine, and epinephrine generally are not (Gillis and Greene 1977). [Pg.411]

In isolated male Sprague-Dawley rat lungs perfused for 6 min at 10 ml/min by a peristaltic pump, H-L-norepinephrine (10 pM) was rapidly deaminated and 0-methylated, and the metabolic products were subsequently returned to the perfusate (Nicholas... [Pg.411]

FIGURE 27 5 Tyrosine is the biosynthetic precursor to a number of neurotransmit ters Each transformation IS enzyme catalyzed Hydroxy lation of the aromatic ring of tyrosine converts it to 3 4 dihyd roxyphenylalanine (l dopa) decarboxylation of which gives dopamine Hy droxylation of the benzylic carbon of dopamine con verts It to norepinephrine (noradrenaline) and methy lation of the ammo group of norepinephrine yields epi nephrine (adrenaline)... [Pg.1126]

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]

Synthetic chemical approaches to the preparation of carbon-14 labeled materials iavolve a number of basic building blocks prepared from barium [ CJ-carbonate (2). These are carbon [ C]-dioxide [ CJ-acetjlene [U— C]-ben2ene, where U = uniformly labeled [1- and 2- C]-sodium acetate, [ C]-methyl iodide, [ C]-methanol, sodium [ C]-cyanide, and [ CJ-urea. Many compHcated radiotracers are synthesized from these materials. Some examples are [l- C]-8,ll,14-eicosatrienoic acid [3435-80-1] inoxn. [ CJ-carbon dioxide, [ting-U— C]-phenyhsothiocyanate [77590-93-3] ftom [ " CJ-acetjlene, [7- " C]-norepinephrine [18155-53-8] from [l- " C]-acetic acid, [4- " C]-cholesterol [1976-77-8] from [ " CJ-methyl iodide, [l- " C]-glucose [4005-41-8] from sodium [ " C]-cyanide, and [2- " C]-uracil [626-07-3] [27017-27-2] from [ " C]-urea. All syntheses of the basic radioactive building blocks have been described (4). [Pg.438]

The original commercial source of E was extraction from bovine adrenal glands (5). This was replaced by a synthetic route for E and NE (Eig. 1) similar to the original pubHshed route of synthesis (6). Eriedel-Crafts acylation of catechol [120-80-9] with chloroacetyl chloride yields chloroacetocatechol [99-40-1]. Displacement of the chlorine by methylamine yields the methylamine derivative, adrenalone [99-45-6] which on catalytic reduction yields (+)-epinephrine [329-65-7]. Substitution of ammonia for methylamine in the sequence yields the amino derivative noradrenalone [499-61-6] which on reduction yields (+)-norepinephrine [138-65-8]. The racemic compounds were resolved with (+)-tartaric acid to give the physiologically active (—)-enantiomers. The commercial synthesis of E and related compounds has been reviewed (27). The synthetic route for L-3,4-dihydroxyphenylalanine [59-92-7] (l-DOPA) has been described (28). [Pg.355]

CBs, like OPs, can cause a variety of sublethal neurotoxic and behavioral effects. In one study with goldfish Carrasius auratus), Bretaud et al. (2002) showed effects of carbofuran on behavioral end points after prolonged exposure to 5 pg/L of the insecticide. At higher levels of exposure (50 or 500 pg/L), biochemical effects were also recorded, including increases in the levels of norepinephrine and dopamine in the brain. The behavioral endpoints related to both swimming pattern and social interactions. Effects of CBs on the behavior of fish will be discussed further in Chapter 16, Section 16.6.1. [Pg.217]

Kosofsky, B.E. Molliver, M.E. Morrison, J.H. and Foote, S.L. The serotonin and norepinephrine innervation of primary visual cortex in the Cynomolgus monkey (Macaca fascicularis). J Comp Neurol 230 168-178, 1984. [Pg.300]

B42. Booke, M., Hinder, F., McGuire, R., Traber, L. D., and Traber, D. L Nitric oxide synthase inhibition versus norepinephrine for the treatment of hyperdynamic sepsis in sheep. Crit. Care Med. 24, 835-844 (1996). [Pg.110]


See other pages where L-norepinephrine is mentioned: [Pg.500]    [Pg.500]    [Pg.1038]    [Pg.123]    [Pg.22]    [Pg.400]    [Pg.258]    [Pg.259]    [Pg.260]    [Pg.285]    [Pg.228]    [Pg.171]    [Pg.172]    [Pg.831]    [Pg.832]    [Pg.325]    [Pg.162]    [Pg.500]    [Pg.500]    [Pg.1038]    [Pg.123]    [Pg.22]    [Pg.400]    [Pg.258]    [Pg.259]    [Pg.260]    [Pg.285]    [Pg.228]    [Pg.171]    [Pg.172]    [Pg.831]    [Pg.832]    [Pg.325]    [Pg.162]    [Pg.342]    [Pg.273]    [Pg.464]    [Pg.95]    [Pg.2]    [Pg.140]    [Pg.274]    [Pg.1142]    [Pg.1498]    [Pg.199]    [Pg.13]    [Pg.327]    [Pg.229]    [Pg.230]    [Pg.105]    [Pg.30]    [Pg.180]    [Pg.326]   
See also in sourсe #XX -- [ Pg.530 ]

See also in sourсe #XX -- [ Pg.123 ]

See also in sourсe #XX -- [ Pg.25 , Pg.530 ]




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Norepinephrine

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