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1-6 of 6
Keywords: carbidopa
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Articles
Journal:
Clinical Science
Clin Sci (Lond) (1997) 92 (4): 409–414.
Published: 01 April 1997
...G. S. Stokes; J. C. Monaghan; D. N. Pillai 1. Dopamine and prostaglandins are putative endogenous natriuretic hormones. The role of each in facilitating natriuresis induced by intravenous saline infusion was examined in normal volunteers in relation to administration of carbidopa...
Articles
Journal:
Clinical Science
Clin Sci (Lond) (1988) 75 (5): 503–507.
Published: 01 November 1988
... acids l -dopa ( l -3,4-dihydroxyphenylalanine) and 5-hydroxytryptophan. During the final two clearance periods, the peripheral decarboxylase inhibitor, carbidopa ( S -α-hydrazino-3,4-dihydroxy-α-methylbenzenepropanoic acid monohydrate), was infused additionally. 2. Renal formation of dopamine (3,4...
Articles
Journal:
Clinical Science
Clin Sci (Lond) (1987) 73 (2): 151–157.
Published: 01 August 1987
...R. F. Jeffrey; T. M. MacDonald; M. Rutter; S. Freestone; J. Brown; R. R. Samson; M. R. Lee 1. The urine dopamine response to intravenous frusemide (30 mg) was investigated in 15 salt replete male volunteers. The effects of oral indomethacin (100 mg) and oral carbidopa (100 mg) given before...
Articles
Journal:
Clinical Science
Clin Sci (Lond) (1981) 61 (2): 187–190.
Published: 01 August 1981
... received in a randomized order placebo, l-dopa (500 mg, orally) and l-dopa (100 mg, orally) plus carbidopa (35 mg, orally) after pretreatment with carbidopa (50 mg every 6 h for four doses). 3. l-Dopa administration elicited a significant fall in plasma renin activity (PRA) ( P < 0.01 at 120, 150...
Articles
A. Scriabine, C. T. Ludden, C. S. Sweet, C. C. Porter, E. H. Ulm, C. A. Stone, C. J. Watkins, R. J. Wurtman, B. L. Cronin
Journal:
Clinical Science
Clin Sci Mol Med (1978) 55 (s4): 255s–257s.
Published: 01 December 1978
... in mean arterial pressure) at 20–80 mg/kg intraperitoneally or 80 mg/kg orally. The maximal effect is reached at 4 h after treatment and the duration of action exceeds 12 h. 2. A peripheral inhibitor of amino acid decarboxylase, carbidopa ([—]-l-α-hydrazino-3,4-dihydroxy-α-methylbenzenepropanoic acid...
Articles
Journal:
Clinical Science
Clin Sci Mol Med (1976) 51 (s3): 407s–410s.
Published: 01 December 1976
...A. Scriabine; C. T. Ludden; C. A. Stone; R. J. Wurtman; C. J. Watkins 1. A peripheral inhibitor of l-aromatic amino acid decarboxylase, carbidopa [(—)-l-α-hydrazino-3,4-dihydroxy-α-methylbenzenepropanoic acid monohydrate], at doses up to 25 mg/kg intraperitoneally or 30 mg/kg orally had no effect...