Hepatic blood flow and metabolism in severe falciparum malaria: clearance of intravenously administered galactose. 1992

S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

1. Hypoglycaemia and lactic acidosis are important manifestations of severe falciparum malaria. To investigate hepatic gluconeogenesis in acute falciparum malaria, liver blood flow and galactose clearance were estimated in seven adult patients with moderately severe infection and seven patients with severe infection (three of whom died later). Nine patients were restudied in convalescence. 2. Liver blood flow, determined from the plasma clearance of Indocyanine Green, was lower in acute illness than in convalescence [16.1 (7.0) versus 23.9 (7.2) ml min-1 kg-1, mean (SD)], but this difference was not statistically significant (P = 0.15). There was a significant inverse correlation between admission venous plasma lactate concentrations and the liver blood flow estimated from the clearance of Indocyanine Green (rs = 0.71, P = 0.004). 3. The plasma clearance of galactose after intravenous injection was similar in the acute [15.4 (4.90) ml min-1 kg-1] and convalescent study [12.8 (2.1) ml min-1 kg-1]. The ratio of galactose clearance to Indocyanine Green clearance was significantly higher in acute disease [1.41 (0.51)] than in convalescence [0.70 (0.34)], largely because of the elevated ratios in severely ill patients [1.48 (0.50)]. 4. The rise in blood glucose concentration after galactose administration was significantly higher during acute illness [1.48 (0.72) mmol/l] than in convalescence [0.67 (0.41) mmol/l, P = 0.022], but the insulin response was similar, indicating reduced tissue insulin sensitivity. There was no significant change in the plasma concentrations of other metabolites (lactate, pyruvate, alanine and triacylglycerol) in either study. 5. These results suggest that the segment of the glycolytic pathway between galactose and glucose is unimpaired in patients with severe falciparum malaria.(ABSTRACT TRUNCATED AT 250 WORDS)

UI MeSH Term Description Entries
D007773 Lactates Salts or esters of LACTIC ACID containing the general formula CH3CHOHCOOR.
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D008102 Liver Circulation The circulation of BLOOD through the LIVER. Hepatic Circulation,Circulation, Liver,Circulation, Hepatic
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D001786 Blood Glucose Glucose in blood. Blood Sugar,Glucose, Blood,Sugar, Blood
D005260 Female Females
D005690 Galactose An aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. Deficiency of galactosyl-1-phosphate uridyltransferase (GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE DEFICIENCY DISEASE) causes an error in galactose metabolism called GALACTOSEMIA, resulting in elevations of galactose in the blood. D-Galactose,Galactopyranose,Galactopyranoside,D Galactose
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000208 Acute Disease Disease having a short and relatively severe course. Acute Diseases,Disease, Acute,Diseases, Acute

Related Publications

S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
February 1994, Annals of tropical medicine and parasitology,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
January 1989, Gastroenterology,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
May 1989, The American journal of tropical medicine and hygiene,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
February 1958, Clinical science,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
October 1983, Gastroenterology,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
October 1988, Gastroenterology,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
January 1971, Acta chirurgica Academiae Scientiarum Hungaricae,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
February 1988, Gastroenterology,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
November 1986, The Journal of surgical research,
S Pukrittayakamee, and N J White, and T M Davis, and S Looareesuwan, and W Supanaranond, and V Desakorn, and B Chaivisuth, and D H Williamson
June 1987, Bollettino della Societa italiana di biologia sperimentale,
Copied contents to your clipboard!