Artículo

Del C. Batlle, A.M.; Fukuda, H.; Parera, V.E.; Wider, E.; Stella, A.M. "In inherited porphyrias, lead intoxication is a toxogenetic disorder" (1987) International Journal of Biochemistry. 19(8):717-720
Estamos trabajando para incorporar este artículo al repositorio
Consulte el artículo en la página del editor
Consulte la política de Acceso Abierto del editor

Abstract:

1. 1. δ-Aminolevulinic acid dehydratase (ALA-D), blood lead and several enzymes and metabolites of the heme biosynthetic pathway were measured in a number of symptomatic porphyric patients, 22 with acute intermittent porphyria, three with hereditary hepatic coproporphyria, 10 with hereditary porphyria cutanea tarda, two with erythropoietic protoporphyria and two with congenital erythropoietic porphyria and in 84 lead intoxicated persons. 2. 2. In the 39 individuals suffering from the inherited porphyrias and in 32 lead poisoned patients with a 30-50% reduced deaminase, blood lead content was not sufficiently increased (average 28 μg%) to account for the greatly decreased activity of ALA-D (average 36% of controls). 3. 3. After a relatively trifling lead exposure they developed the signs of acute lead intoxication. 4. 4. A second group of lead intoxicated patients showing low ALA-D activity and corresponding high concentration of lead in blood, exhibited no other physiologic deviation in the enzymes and metabolites of porphyrin biosynthesis. 5. 5. Individuals with inherited porphyrias are ultrasensitive to low level lead exposure and that lead would also act as a triggering factor. In these patients, lead intoxication can be considered a toxogenetic disorder. 6. 6. An inversely linear correlation between ALA-D activity and blood lead content was obtained for both groups of lead intoxicated patients, however, a different constant (k) for each was obtained, which we have taken as a measure of lead toxogeneticity: k = 10 ± 1 for lead intoxicated individuals with otherwise normal heme metabolism and k = 5 ± 0.5 for lead intoxicated symptomatic porphyric patients. 7. 7. Determination of erythrocytic ALA-D, besides blood lead, will be a valuable indicator for preventive medical care for these patients, when they are expected to be exposed to lead either environmentally or in their professional life. © 1987.

Registro:

Documento: Artículo
Título:In inherited porphyrias, lead intoxication is a toxogenetic disorder
Autor:Del C. Batlle, A.M.; Fukuda, H.; Parera, V.E.; Wider, E.; Stella, A.M.
Filiación:Centro de Investigaciones sobre Porfirinas y Porfirias, CIPYP (Consejo Nacional de Investigaciones Cientificas y Tecnicas, CONICET, y Facultad de Ciencias E, C. Universitaria, Pab. II, 1428 Buenos Aires, Argentina
Palabras clave:lead; porphobilinogen synthase; acute intermittent porphyria; blood; blood and hemopoietic system; congenital disorder; congenital erythropoietic porphyria; erythropoietic protoporphyria; etiology; human; intoxication; lead poisoning; porphyria; porphyria cutanea tarda; priority journal; review; Heme; Humans; Lead; Lead Poisoning; Porphobilinogen Synthase; Porphyrias
Año:1987
Volumen:19
Número:8
Página de inicio:717
Página de fin:720
DOI: http://dx.doi.org/10.1016/0020-711X(87)90086-3
Título revista:International Journal of Biochemistry
Título revista abreviado:Int. J. Biochem.
ISSN:0020711X
CODEN:IJBOB
CAS:lead, 13966-28-4, 7439-92-1; porphobilinogen synthase, 9036-37-7; Heme, 14875-96-8; Lead, 7439-92-1; Porphobilinogen Synthase, 4.2.1.24
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0020711X_v19_n8_p717_DelCBatlle

Referencias:

  • Abdulla, Hager-Arönsen, Svensson, Effect of ethanol and zinc on ALA-dehydratase activity in red blood cells (1976) Enzyme, 21, pp. 248-258
  • Afonso, Chinarro Familiar, Stella, Batlle A.M. del, Lenczner, Magnin, Uroporfirinógeno decarboxilasa eritrocitaria y hepática en porfiria cutánea tardia (1985) Rev. Arg. Derm., 66, pp. 12-24
  • Batlle A.M. del, Wider de Xifra, Stella, A simple method for measuring erythrocyte porphobilinogenase and its use in the diagnosis of acute intermittent porphyria (1978) Int. J. Biochem., 9, pp. 871-875
  • Batlle A.M. del, Wider de Xifra, Stella, Bustos, With, Studies on porphyrin biosynthesis and the enzymes involved in bovine congenital erythropoietic porphyria (1979) Clin. Sci., 57, pp. 63-70
  • Batlle A.M. del, Bustos, Stella, Wider, Conti, Méndez, Enzyme replacement therapy in porphyrias IV. First successful human clinical trial of δ-aminolevulinate dehydratase-loaded erythyrocyte ghosts (1983) Int. J. Biochem., 15, pp. 1261-1265
  • Bonsignore, δ-Aminolevulinate dehydratase activity of erythrocytes as a diagnostic test in occupational lead poisoning (1966) Med. Lav., 57, pp. 647-650
  • Doss, Tiepermann, Schneider, Schmid, New type of hepatic porphyria with Porphobilinogenase defect and intermittent acute clinical manifestation (1979) Klin. Wochenschr., 57, pp. 1123-1133
  • Doss, Becker, Sixel, Geisse, Solcher, Schneider, Persistent protoporphyrinemia in hereditary porphobilinogen synthase ((5-aminolevulinic acid dehydrase). Deficiency under low lead exposure (1982) Klin. Wochenschr., 60, pp. 599-607
  • Doss, Laubenthal, Stoepler, Lead poisoning in inherited δ-aminolevulinic acid dehydratase deficiency (1984) Int. Archs occup. Environ. Hlth, 54, pp. 55-65
  • Hernberg, Nikkanen, Effect of lead on δ-aminolevulinic dehydratase. A selective review (1972) Praconvi Lekarstvi, 24, pp. 77-87
  • Lindblad, Lindstedt, Steen, On the enzymic defects in hereditary tyrosinemia (1977) Proc. natn. Acad. Sci., U.S.A., 74, pp. 4641-4645
  • Moore, Meredith, Goldberg, Lead and heme biosynthesis (1980) Lead Toxicity, pp. 79-89. , R.L. Singhai, J.A. Thomas, Urban & Schwarzenberg, Baltimore, Md
  • Poh-Fitzpatrick, Lamola, Direct spectrofluorometry of diluted erythrocytes and plasma. A rapid diagnostic method in primary and secondary porphyrinemias (1976) J. Lab. clin. Med., 87, pp. 362-366
  • Rao, Pandya, Hepatic metabolism of heme in rats after exposure to benzene, gasoline and kerosene (1980) Archs Toxic., 46, pp. 313-317
  • Salle, Zielhuis, Influence of smoking on ALA-D activity, hematocrite and lead in blood in adult urban women (1977) Int. Archs occup. Environ. Hlth, 40, pp. 111-115
  • Schoua, Batlle A.M. del, Indice de porfirinas plasmaticas (1987) Rev. Arg. Derm., 68, pp. 79-85
  • Stella, Wider E. A. de, Lenczner, Magnin, Batlle A. M. del, Aspectos bio-químicos y enzimáticos en la protoporfiria humana (1981) Rev. Arg. Derm., 62, pp. 7-13

Citas:

---------- APA ----------
Del C. Batlle, A.M., Fukuda, H., Parera, V.E., Wider, E. & Stella, A.M. (1987) . In inherited porphyrias, lead intoxication is a toxogenetic disorder. International Journal of Biochemistry, 19(8), 717-720.
http://dx.doi.org/10.1016/0020-711X(87)90086-3
---------- CHICAGO ----------
Del C. Batlle, A.M., Fukuda, H., Parera, V.E., Wider, E., Stella, A.M. "In inherited porphyrias, lead intoxication is a toxogenetic disorder" . International Journal of Biochemistry 19, no. 8 (1987) : 717-720.
http://dx.doi.org/10.1016/0020-711X(87)90086-3
---------- MLA ----------
Del C. Batlle, A.M., Fukuda, H., Parera, V.E., Wider, E., Stella, A.M. "In inherited porphyrias, lead intoxication is a toxogenetic disorder" . International Journal of Biochemistry, vol. 19, no. 8, 1987, pp. 717-720.
http://dx.doi.org/10.1016/0020-711X(87)90086-3
---------- VANCOUVER ----------
Del C. Batlle, A.M., Fukuda, H., Parera, V.E., Wider, E., Stella, A.M. In inherited porphyrias, lead intoxication is a toxogenetic disorder. Int. J. Biochem. 1987;19(8):717-720.
http://dx.doi.org/10.1016/0020-711X(87)90086-3