Literature DB >> 3945626

A highly sensitive assay for phenylethanolamine N-methyltransferase in human brain.

W J Burke, D M Hanson, H D Chung.   

Abstract

A rapid, highly sensitive assay for phenylethanolamine N-methyltransferase in brain using the natural substrate, norepinephrine, is described. The method is based on the selective adsorption and elution of the reaction product, epinephrine, from alumina. A small but important further lowering of blanks and increase in sensitivity is attained by removal of the radiolabeled substrate, [methyl-3H]-S-adenosylmethionine by precipitation as the reineckate prior to adsorption of norepinephrine to alumina. The assay has a sensitivity of 30 fmole and the PNMT activity could be measured in as little as 1 mg (wet wt) of human locus coeruleus tissue. The sensitivity is enhanced by homogenizing tissue in small volumes and removing potential inhibitors by dialysis. We report for the first time PNMT activity in specific regions of the human cerebral and cerebellar cortex.

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Year:  1986        PMID: 3945626     DOI: 10.3181/00379727-181-42225

Source DB:  PubMed          Journal:  Proc Soc Exp Biol Med        ISSN: 0037-9727


  2 in total

1.  Molecular cloning and characterization of an L-epinephrine transporter from sympathetic ganglia of the bullfrog, Rana catesbiana.

Authors:  S Apparsundaram; K R Moore; M D Malone; H C Hartzell; R D Blakely
Journal:  J Neurosci       Date:  1997-04-15       Impact factor: 6.167

2.  Double stable isotope ultra performance liquid chromatographic-tandem mass spectrometric quantification of tissue content and activity of phenylethanolamine N-methyltransferase, the crucial enzyme responsible for synthesis of epinephrine.

Authors:  Nan Qin; Mirko Peitzsch; Mario Menschikowski; Gabriele Siegert; Karel Pacak; Graeme Eisenhofer
Journal:  Anal Bioanal Chem       Date:  2012-12-08       Impact factor: 4.142

  2 in total

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