Page last updated: 2024-10-20

pyruvic acid and Acidosis, Lactic

pyruvic acid has been researched along with Acidosis, Lactic in 51 studies

Pyruvic Acid: An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed)
pyruvic acid : A 2-oxo monocarboxylic acid that is the 2-keto derivative of propionic acid. It is a metabolite obtained during glycolysis.

Acidosis, Lactic: Acidosis caused by accumulation of lactic acid more rapidly than it can be metabolized. It may occur spontaneously or in association with diseases such as DIABETES MELLITUS; LEUKEMIA; or LIVER FAILURE.

Research Excerpts

ExcerptRelevanceReference
"Pyruvate Ringer's solution efficiently treated hypoxic lactic acidosis and significantly increased the survival rate in rats with lethal hemorrhagic shock."7.79Pyruvate Ringer's solution corrects lactic acidosis and prolongs survival during hemorrhagic shock in rats. ( Bai, XD; Fang, T; Hu, S; Liu, XQ; Wang, HB; Zhong, YX; Zhou, FQ, 2013)
"Although the blood lactate-to-pyruvate (L:P) molar ratio is used to distinguish between pyruvate dehydrogenase deficiency (PDH-D) and other causes of congenital lactic acidosis (CLA), its diagnostic accuracy for differentiating between these 2 types of CLA has not been evaluated formally."7.74Diagnostic accuracy of blood lactate-to-pyruvate molar ratio in the differential diagnosis of congenital lactic acidosis. ( Allard, P; Debray, FG; Hanley, JA; Lambert, M; Mitchell, GA; Robinson, BH, 2007)
" We propose low molar ratios of ketone bodies in plasma of neonates with congenital lactic acidosis as an indication of dysfunction of the tricarboxylic acid cycle."7.68Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis. ( Aupetit, J; Bonnefont, JP; Charpentier, C; Chretien, D; Munnich, A; Rabier, D; Robinson, B; Rustin, P; Saudubray, JM; Vassault, A, 1992)
"A mitochondrial defect was investigated in an infant with fatal congenital lactic acidosis (3-14 mM), high lactate-to-pyruvate ratio, hypotonia, and cardiomyopathy."7.67Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy. ( Dahms, B; Hoppel, CL; Kerr, DS; Roessmann, U, 1987)
"Treatment with thiamine and carnitine resulted in a decrease in blood lactate to normal levels and a dramatic clinical improvement."5.28Neonatal cardiomyopathy and lactic acidosis responsive to thiamine. ( Abeling, NG; Bakker, HD; Lam, J; Luyt-Houwen, IE; Scholte, HR; van Gennip, AH, 1991)
" However, the mutual dependence between lactate dehydrogenase (LDH) catalytic action and lactic acidosis is far from being fully understood."4.12Allosteric transitions of rabbit skeletal muscle lactate dehydrogenase induced by pH-dependent dissociation of the tetrameric enzyme. ( Binda, C; Brigotti, M; Cerini, S; Dal Piaz, F; Di Stefano, G; Hochkoeppler, A; Iacovino, LG; Pasti, AP; Rossi, M; Rossi, V; Tomaselli, F, 2022)
" A 48-week, prospective, single-centre, exploratory, clinical study enrolled 11 Japanese adult patients with genetically, biochemically, and clinically confirmed mitochondrial disease; they had intractable lactic acidosis and received SP (0."3.91Biomarkers and clinical rating scales for sodium pyruvate therapy in patients with mitochondrial disease. ( Inoue, E; Koga, Y; Nashiki, K; Povalko, N; Tanaka, M, 2019)
"Lactic acidosis during metformin intoxication is classically mainly attributed to diminished lactate clearance through liver gluconeogenesis."3.83Skeletal muscle lactate overproduction during metformin intoxication: An animal study with reverse microdialysis. ( Bassani, G; Ferrero, S; Gattinoni, L; Guenzani, S; Langer, T; Magnoni, S; Properzi, P; Protti, A; Santini, A; Stocchetti, N, 2016)
"Pyruvate Ringer's solution efficiently treated hypoxic lactic acidosis and significantly increased the survival rate in rats with lethal hemorrhagic shock."3.79Pyruvate Ringer's solution corrects lactic acidosis and prolongs survival during hemorrhagic shock in rats. ( Bai, XD; Fang, T; Hu, S; Liu, XQ; Wang, HB; Zhong, YX; Zhou, FQ, 2013)
"Although the blood lactate-to-pyruvate (L:P) molar ratio is used to distinguish between pyruvate dehydrogenase deficiency (PDH-D) and other causes of congenital lactic acidosis (CLA), its diagnostic accuracy for differentiating between these 2 types of CLA has not been evaluated formally."3.74Diagnostic accuracy of blood lactate-to-pyruvate molar ratio in the differential diagnosis of congenital lactic acidosis. ( Allard, P; Debray, FG; Hanley, JA; Lambert, M; Mitchell, GA; Robinson, BH, 2007)
"During constant work-rate exercise above the lactic acidosis threshold, oxygen consumption fails to plateau by 3 minutes, but continues to rise slowly."3.72Gas exchange responses to constant work-rate exercise in patients with glycogenosis type V and VII. ( Lovell, S; Nicholls, DP; O'Dochartaigh, CS; Ong, HY; Patterson, VH; Riley, MS; Wasserman, K, 2004)
"Sixty consecutive adult patients who developed septic shock and lactic acidosis requiring the administration of vasopressors."3.70Evolution of lactate/pyruvate and arterial ketone body ratios in the early course of catecholamine-treated septic shock. ( Bollaert, PE; Gelot, AM; Larcan, A; Levy, B; Nabet, P; Sadoune, LO, 2000)
" Hyperlactatemia with L/P ratio elevation and lactic acidosis is likely to be associated with inadequate tissue perfusion."3.70Time-pattern of lactate and lactate to pyruvate ratio in the first 24 hours of intensive care emergency admissions. ( Kari, A; Ruokonen, E; Suistomaa, M; Takala, J, 2000)
" Above the anaerobic threshold, accelerated glycolysis increases muscle lactic acidosis."3.69Determination of the anaerobic threshold by gas exchange: biochemical considerations, methodology and physiological effects. ( Casaburi, R; Cooper, CB; Koike, A; Stringer, WW; Wasserman, K, 1994)
" The lactic acidosis threshold and VO2 kinetics were examined."3.68Is the anaerobic threshold truly anaerobic? ( Koike, A; Wasserman, K, 1992)
" We propose low molar ratios of ketone bodies in plasma of neonates with congenital lactic acidosis as an indication of dysfunction of the tricarboxylic acid cycle."3.68Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis. ( Aupetit, J; Bonnefont, JP; Charpentier, C; Chretien, D; Munnich, A; Rabier, D; Robinson, B; Rustin, P; Saudubray, JM; Vassault, A, 1992)
"We report a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes who experienced visual and auditory hallucinations."3.68Therapeutic effect of sodium dichloroacetate on visual and auditory hallucinations in a patient with MELAS. ( Hashimoto, T; Ito, M; Kuroda, Y; Naito, E; Saijo, T; Takeda, E, 1991)
" Patients with mitochondrial encephalopathy with lactic acidosis and stroke-like episodes demonstrated only minor changes in redox state and in the behavior of the mitochondrial respiratory chain."3.68The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lacticacidemia. ( Capaldi, R; Chow, W; Glerum, DM; Lightowlers, R; Petrova-Benedict, R; Robinson, BH, 1990)
"A mitochondrial defect was investigated in an infant with fatal congenital lactic acidosis (3-14 mM), high lactate-to-pyruvate ratio, hypotonia, and cardiomyopathy."3.67Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy. ( Dahms, B; Hoppel, CL; Kerr, DS; Roessmann, U, 1987)
"We have investigated the effect of dichloroacetate (DCA) on the urinary excretion of lactate and pyruvate in a patient with congenital lactic acidosis and in healthy human controls."3.67Renal effects of dichloroacetate in vivo. ( Kamoshita, S; Kodama, H; Kodama, M; Okabe, I; Orii, T; Yamaguchi, S, 1986)
"Early-onset hyperlactatemia is that which develops in the operating room or very early following intensive care unit (ICU) admission."2.55Hyperlactatemia and Cardiac Surgery. ( Minton, J; Sidebotham, DA, 2017)
"Hypoxic lactic acidosis was efficiently reversed in group PR, instead of group CR, (pH 7."1.48Pyruvate in reduced osmolarity oral rehydration salt corrected lactic acidosis in sever scald rats. ( Li, ZY; Liu, R; Wang, SM; Yu, W; Zhang, HP; Zhou, FQ, 2018)
"Hypoxic lactic acidosis was fully corrected in group PORS in 4 h, whereas it worsened in group BORS, and the 24-h survival rate was twice higher in group PORS than in group BORS (45."1.42Pyruvate oral rehydration solution improved visceral function and survival in shock rats. ( He, ZJ; Hu, S; Lin, HY; Luo, HM; Sheng, ZY; Xie, ZY; Yu, W; Zhou, FQ, 2015)
"Children with MELAS had various clinical manifestations."1.39[Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children]. ( Bao, XH; Chang, XZ; Liu, XL; Ma, YN; Qin, J; Wu, XR, 2013)
"Both steroids and hemorrhage may affect the hepatic energy metabolism."1.30[Effects of steroids on hepatic ATP and L/P ratio in rats subjected to acute hemorrhage]. ( Ikeya, K; Kashimoto, S; Kumazawa, T; Kume, M, 1997)
"The majority of patients with PDHC deficiency have abnormalities in the major catalytic and regulatory subunit, E1 alpha, which is encoded on the X chromosome."1.29Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency. ( Arnold, DL; Brown, GK; Brown, RM; Legris, M; Matthews, PM; Otero, LJ; Scriver, CR; Shevell, MI, 1994)
"Treatment with thiamine and carnitine resulted in a decrease in blood lactate to normal levels and a dramatic clinical improvement."1.28Neonatal cardiomyopathy and lactic acidosis responsive to thiamine. ( Abeling, NG; Bakker, HD; Lam, J; Luyt-Houwen, IE; Scholte, HR; van Gennip, AH, 1991)
"Pyruvate dehydrogenase complex deficiency is thought to be a common cause of lactic acidosis."1.27Fatal lactic acidosis due to deficiency of E1 component of the pyruvate dehydrogenase complex. ( Aynsley-Green, A; Birch-Machin, MA; Gardner-Medwin, D; Lindsay, JG; Shepherd, IM; Sherratt, HS; Solomon, M; Turnbull, DM; Yeaman, SJ, 1988)

Research

Studies (51)

TimeframeStudies, this research(%)All Research%
pre-19906 (11.76)18.7374
1990's14 (27.45)18.2507
2000's13 (25.49)29.6817
2010's16 (31.37)24.3611
2020's2 (3.92)2.80

Authors

AuthorsStudies
Iacovino, LG1
Rossi, M1
Di Stefano, G1
Rossi, V1
Binda, C1
Brigotti, M1
Tomaselli, F1
Pasti, AP1
Dal Piaz, F1
Cerini, S1
Hochkoeppler, A1
Li, J1
Yang, Y1
Peng, Z1
Yang, J2
Li, Y1
Liu, R1
Wang, SM1
Li, ZY1
Yu, W2
Zhang, HP1
Zhou, FQ4
Wang, Y1
Huang, Y1
Zhao, L1
Zhou, H1
Koga, Y1
Povalko, N1
Inoue, E1
Nashiki, K1
Tanaka, M1
Katsu-Jiménez, Y1
Vázquez-Calvo, C1
Maffezzini, C1
Halldin, M1
Peng, X1
Freyer, C1
Wredenberg, A1
Giménez-Cassina, A1
Wedell, A1
Arnér, ESJ1
Ambrus, A1
Liu, XL1
Bao, XH1
Ma, YN1
Chang, XZ1
Qin, J1
Wu, XR1
Ching, CK1
Mak, CM1
Au, KM1
Chan, KY1
Yuen, YP1
Yau, EK1
Ma, LC1
Chow, HL1
Chan, AY1
Hu, S2
Bai, XD1
Liu, XQ1
Wang, HB1
Zhong, YX1
Fang, T1
Moustafa, F1
Garrouste, C1
Bertrand, PM1
Kauffmann, S1
Schmidt, J1
Xie, ZY1
He, ZJ1
Luo, HM1
Lin, HY1
Sheng, ZY1
Danhauser, K1
Smeitink, JA1
Freisinger, P2
Sperl, W2
Sabir, H1
Hadzik, B1
Mayatepek, E1
Morava, E1
Distelmaier, F1
Protti, A1
Properzi, P1
Magnoni, S1
Santini, A1
Langer, T1
Guenzani, S1
Ferrero, S1
Bassani, G1
Stocchetti, N1
Gattinoni, L1
Minton, J1
Sidebotham, DA1
Kovacevic, A1
Schwahn, B1
Schuster, A1
Levy, B2
Perez, P1
Perny, J1
Thivilier, C1
Gerard, A1
Mayr, JA1
Schlachter, K1
Rolinski, B1
Zimmermann, FA1
Scheffner, T1
Haack, TB1
Koch, J1
Ahting, U1
Prokisch, H1
Schurr, A1
Totani, M1
Ong, HY1
O'Dochartaigh, CS1
Lovell, S1
Patterson, VH1
Wasserman, K4
Nicholls, DP1
Riley, MS1
Seino, H1
Hiraizumi, M1
Dote, T1
Kono, K1
Usuda, K1
Shimizu, H1
Tanimoto, Y1
Dote, E1
Hayashi, S1
Gutierrez, G1
Wulf, ME1
Debray, FG1
Mitchell, GA1
Allard, P1
Robinson, BH2
Hanley, JA1
Lambert, M1
Hosein, RB1
Morris, KP1
Brawn, WJ1
Barron, DJ1
Shevell, MI1
Matthews, PM1
Scriver, CR1
Brown, RM1
Otero, LJ1
Legris, M1
Brown, GK1
Arnold, DL1
Stringer, WW1
Casaburi, R1
Koike, A2
Cooper, CB1
Yuan, XQ1
Wade, CE1
Feriani, M1
Ikeya, K1
Kashimoto, S1
Kume, M1
Kumazawa, T1
Sadoune, LO1
Gelot, AM1
Bollaert, PE1
Nabet, P1
Larcan, A1
Suistomaa, M1
Ruokonen, E1
Kari, A1
Takala, J1
Arbour, R1
Esparis, B1
Giordano, G1
Corradi, D1
D'Adda, T1
Melissari, M1
Hirai, M1
Suzuki, S1
Ito, M3
Kobashi, H3
Naito, E5
Saijo, T3
Takeda, E4
Huq, AH1
Kuroda, Y5
Merinero, B1
Pérez-Cerda, C1
Ugarte, M1
Bonnefont, JP1
Chretien, D1
Rustin, P1
Robinson, B1
Vassault, A1
Aupetit, J1
Charpentier, C1
Rabier, D1
Saudubray, JM1
Munnich, A1
Bakker, HD1
Scholte, HR1
Luyt-Houwen, IE1
van Gennip, AH1
Abeling, NG1
Lam, J1
Abe, K1
Fujimura, H1
Nishikawa, Y1
Yorifuji, S1
Mezaki, T1
Hirono, N1
Nishitani, N1
Kameyama, M1
Hashimoto, T1
Glerum, DM1
Chow, W1
Petrova-Benedict, R1
Lightowlers, R1
Capaldi, R1
Beaver, WL1
Whipp, BJ1
Toshima, K1
Yokota, I2
Miyao, M1
Hoppel, CL1
Kerr, DS1
Dahms, B1
Roessmann, U1
Birch-Machin, MA1
Shepherd, IM1
Solomon, M1
Yeaman, SJ1
Gardner-Medwin, D1
Sherratt, HS1
Lindsay, JG1
Aynsley-Green, A1
Turnbull, DM1
Kodama, H1
Yamaguchi, S1
Okabe, I1
Kodama, M1
Orii, T1
Kamoshita, S1

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Mean Arterial Pressure (MAP) Trial: Study Protocol for a Multicenter, Randomized, Controlled Trial to Compare Three Different Strategies of Mean Arterial Pressure Management During Cardiopulmonary By-pass[NCT05740397]900 participants (Anticipated)Interventional2021-05-03Recruiting
"Influence of High Vitamin C Dose on Lactate During Extracorporeal Circulation for Heart Surgery and During the 24 Hours Thereafter. (Double Blind Prospective Randomised Study)"[NCT04046861]200 participants (Anticipated)Interventional2023-02-01Not yet recruiting
Phase 3 Trial of Coenzyme Q10 in Mitochondrial Disease[NCT00432744]Phase 324 participants (Actual)Interventional2007-01-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

McMaster Gross Motor Function (GMFM 88)

The McMaster Gross Motor Function is a validated scale ranging from 0 to 100 (the higher the better). Since there was the possibility of a subject becoming totally disabled our FDA peer reviewed design called for its use as follows: If the subject completed both periods, the score was calculated as the difference in scores between the end of Period 2 (at 12 months) minus that at the end of Period 1 (6 months). If a subject became totally disabled, this difference was considered as plus infinity if it occurred in period 1 (Penalizes period 1), and minus infinity if it occurred in Period 2 (Penalizes period 2). The two treatments were compared via the Wilcoxon test, and the effect size was estimated using Kendall's Tau-B. This is interpreted in a similar manner to correlation with positive values favoring COQenzyme10 and negative values favoring placebo. One of the links in this report is to the the GMFM scale and how it is scored. A link to the instrument is included. (NCT00432744)
Timeframe: Taken at 6 and 12 Months

Interventionunits on a scale (Median)
Placebo First-0.002
CoenzymeQ10 Frist-0.12

Non-parametric Hotelling T-square Bivariate Analysis of GMGF 88 and OPeds QOL.

This is a multivariate analysis of the first two outcomes: Period 2 minus Period 1 GMFM88 and Peds Quality of Life, analyzed as follows: First, to be in the analysis, subjects must contribute at least one of these endpoints. Second, if the subject became totally disabled during period 1, the difference was defined as + infinity, (highest possible evidence favoring period 2), and if the subject became totally disabled in period 2, the subject was scored as - infinity (highest possible evidence favoring period 1). Period 2 minus period 1 differences were ranked form low to high with missing values scores at the mid-rank. The Hotelling T-square was computed on these ranks and the P-value was obtained from 100,000 rerandomizations as the fraction of rerandomizations with T-sq at least as large as that observed. (NCT00432744)
Timeframe: end of 12 month minus end of 6 month difference.

Interventionparticipants (Number)
Placebo First7
CoenzymeQ10 Frist8

Pediatric Quality of Life Scale

"The Pediatric Quality of Life Scale is a validated scale ranging from 0 to 100 (the higher the better). Since there was the possibility of a subject becoming totally disabled our FDA peer reviewed design called for its use as follows: If the subject completed both periods, the score was calculated as the difference in scores between the end of Period 2 (at 12 months) minus that at the end of Period 1 (6 months). If a subject became totally disabled, this difference was considered as plus infinity if it occurred in period 1 (Penalizes period 1), and minus infinity if it occurred in Period 2 (Penalizes period 2). The two treatments were compared via the Wilcoxon test, and the effect size was estimated using Kendall's Tau-B. This is interpreted in a similar manner to correlation with positive values favoring COQenzyme10 and negative values favoring placebo. Goggle pedsQL and Mapi to browse the copyrighted manual. A link to the instrument is included." (NCT00432744)
Timeframe: At 6 and 12 Months

Interventionunits on a scale (Median)
Placebo First-1.1
CoenzymeQ10 Frist-11.9

Reviews

10 reviews available for pyruvic acid and Acidosis, Lactic

ArticleYear
Pyruvate is a prospective alkalizer to correct hypoxic lactic acidosis.
    Military Medical Research, 2018, 04-26, Volume: 5, Issue:1

    Topics: Acidosis, Lactic; Antacids; Bicarbonates; Erythropoietin; Fluid Therapy; Humans; Hypoxia; Hypoxia-In

2018
An Updated View on the Molecular Pathomechanisms of Human Dihydrolipoamide Dehydrogenase Deficiency in Light of Novel Crystallographic Evidence.
    Neurochemical research, 2019, Volume: 44, Issue:10

    Topics: Acidosis, Lactic; Amino Acid Oxidoreductases; Cytochrome-B(5) Reductase; Dihydrolipoamide Dehydrogen

2019
Treatment options for lactic acidosis and metabolic crisis in children with mitochondrial disease.
    Journal of inherited metabolic disease, 2015, Volume: 38, Issue:3

    Topics: Acidosis, Lactic; Child; Child, Preschool; Disease Management; Humans; Hypothermia; Mitochondrial Di

2015
Hyperlactatemia and Cardiac Surgery.
    The journal of extra-corporeal technology, 2017, Volume: 49, Issue:1

    Topics: Acidosis, Lactic; Biomarkers; Cardiac Surgical Procedures; Humans; Hyperlactatemia; Hypoxia; Lactic

2017
Lactate, glucose and energy metabolism in the ischemic brain (Review).
    International journal of molecular medicine, 2002, Volume: 10, Issue:2

    Topics: Acidosis, Lactic; Anaerobiosis; Animals; Brain; Brain Damage, Chronic; Brain Ischemia; Corticosteron

2002
[Lactate . pyruvate].
    Nihon rinsho. Japanese journal of clinical medicine, 2002, Volume: 60 Suppl 8

    Topics: Acidosis, Lactic; Biomarkers; Diabetes Mellitus; Humans; Lactic Acid; Neoplasms; Pyruvic Acid

2002
[Progress in diagnosis of and therapy for diabetic lactic acidosis].
    Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 2004, Aug-10, Volume: 93, Issue:8

    Topics: Acid-Base Equilibrium; Acidosis, Lactic; Blood Gas Analysis; Consciousness Disorders; Diabetes Compl

2004
Buffers: bicarbonate, lactate and pyruvate.
    Kidney international. Supplement, 1996, Volume: 56

    Topics: Acidosis, Lactic; Bicarbonates; Buffers; Dialysis Solutions; Humans; Lactic Acid; Peritoneal Dialysi

1996
[Lactic acidosis].
    Nihon rinsho. Japanese journal of clinical medicine, 2002, Volume: 60 Suppl 4

    Topics: Acidosis, Lactic; Diagnosis, Differential; Humans; Mitochondria; Mitochondrial Diseases; Prognosis;

2002
Gas exchange theory and the lactic acidosis (anaerobic) threshold.
    Circulation, 1990, Volume: 81, Issue:1 Suppl

    Topics: Acidosis, Lactic; Anaerobic Threshold; Heart Failure; Humans; Models, Cardiovascular; Oxygen Consump

1990

Trials

1 trial available for pyruvic acid and Acidosis, Lactic

ArticleYear
Comparison of norepinephrine-dobutamine to epinephrine for hemodynamics, lactate metabolism, and organ function variables in cardiogenic shock. A prospective, randomized pilot study.
    Critical care medicine, 2011, Volume: 39, Issue:3

    Topics: Acidosis, Lactic; Aged; Blood Gas Analysis; Blood Pressure; Cardiac Output; Dobutamine; Epinephrine;

2011

Other Studies

40 other studies available for pyruvic acid and Acidosis, Lactic

ArticleYear
Allosteric transitions of rabbit skeletal muscle lactate dehydrogenase induced by pH-dependent dissociation of the tetrameric enzyme.
    Biochimie, 2022, Volume: 199

    Topics: Acidosis, Lactic; Animals; Citrates; Hydrogen-Ion Concentration; Kinetics; L-Lactate Dehydrogenase;

2022
A novel photoelectrochemical microfluidic chip for multi-index determination of diabetes and its complications.
    Biosensors & bioelectronics, 2022, Dec-01, Volume: 217

    Topics: 3-Hydroxybutyric Acid; Acidosis, Lactic; Biomarkers; Biosensing Techniques; Diabetes Mellitus; Diabe

2022
Pyruvate in reduced osmolarity oral rehydration salt corrected lactic acidosis in sever scald rats.
    The Journal of surgical research, 2018, Volume: 226

    Topics: Acidosis, Lactic; Administration, Oral; Animals; Bicarbonates; Burns; Citric Acid; Disease Models, A

2018
Biomarkers and clinical rating scales for sodium pyruvate therapy in patients with mitochondrial disease.
    Mitochondrion, 2019, Volume: 48

    Topics: Acidosis, Lactic; Adolescent; Adult; Biomarkers; Female; Fibroblast Growth Factors; Growth Different

2019
Absence of TXNIP in Humans Leads to Lactic Acidosis and Low Serum Methionine Linked to Deficient Respiration on Pyruvate.
    Diabetes, 2019, Volume: 68, Issue:4

    Topics: Acidosis, Lactic; Carrier Proteins; Child; Child, Preschool; Female; Fibroblasts; Glycolysis; Humans

2019
[Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2013, Volume: 51, Issue:2

    Topics: Acidosis, Lactic; Adolescent; Brain; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochon

2013
A patient with congenital hyperlactataemia and Leigh syndrome: an uncommon mitochondrial variant.
    Hong Kong medical journal = Xianggang yi xue za zhi, 2013, Volume: 19, Issue:4

    Topics: Acidosis, Lactic; DNA, Mitochondrial; Female; Humans; Infant; Lactic Acid; Leigh Disease; Pyruvic Ac

2013
Pyruvate Ringer's solution corrects lactic acidosis and prolongs survival during hemorrhagic shock in rats.
    The Journal of emergency medicine, 2013, Volume: 45, Issue:6

    Topics: Acidosis, Lactic; Analysis of Variance; Animals; Arterial Pressure; Carbon Dioxide; Disease Models,

2013
[Lactic acidosis after inhaled beta-2 agonists: about 2 cases].
    Annales francaises d'anesthesie et de reanimation, 2014, Volume: 33, Issue:1

    Topics: Acidosis, Lactic; Administration, Inhalation; Adrenergic beta-2 Receptor Agonists; Albuterol; Asthma

2014
Pyruvate oral rehydration solution improved visceral function and survival in shock rats.
    The Journal of surgical research, 2015, Volume: 193, Issue:1

    Topics: Acidosis, Lactic; Animals; Bicarbonates; Disease Models, Animal; Fluid Therapy; Glucose; Lipid Perox

2015
Skeletal muscle lactate overproduction during metformin intoxication: An animal study with reverse microdialysis.
    Toxicology letters, 2016, Jul-25, Volume: 255

    Topics: Acidosis, Lactic; Animals; Glycolysis; Hypoglycemic Agents; Infusions, Parenteral; Lactic Acid; Metf

2016
Hyperlactic acidosis as metabolic side-effect of albuterol and theophylline in acute severe asthma.
    Klinische Padiatrie, 2010, Volume: 222, Issue:4

    Topics: Acidosis, Lactic; Administration, Inhalation; Adolescent; Albuterol; Anti-Asthmatic Agents; Anti-Inf

2010
Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway.
    American journal of human genetics, 2011, Dec-09, Volume: 89, Issue:6

    Topics: Abnormalities, Multiple; Acidosis, Lactic; Adolescent; Amino Acid Sequence; Base Sequence; Brain Dis

2011
Gas exchange responses to constant work-rate exercise in patients with glycogenosis type V and VII.
    American journal of respiratory and critical care medicine, 2004, Jun-01, Volume: 169, Issue:11

    Topics: Acidosis, Lactic; Adult; Case-Control Studies; Epinephrine; Exercise; Exercise Test; Exercise Tolera

2004
Systemic effects and skin injury after experimental dermal exposure to monochloroacetic acid.
    Toxicology and industrial health, 2003, Volume: 19, Issue:7-10

    Topics: Accidents, Occupational; Acetates; Acidosis, Lactic; Animals; Blood Chemical Analysis; Burns, Chemic

2003
Lactic acidosis in sepsis: another commentary.
    Critical care medicine, 2005, Volume: 33, Issue:10

    Topics: Acidosis, Lactic; Glucose; Humans; Lactic Acid; Pyruvic Acid; Sepsis

2005
Diagnostic accuracy of blood lactate-to-pyruvate molar ratio in the differential diagnosis of congenital lactic acidosis.
    Clinical chemistry, 2007, Volume: 53, Issue:5

    Topics: Acidosis, Lactic; Child; Diagnosis, Differential; Female; Hospitals, Pediatric; Humans; Lactic Acid;

2007
Use of tissue microdialysis to investigate hyperlactataemia following paediatric cardiac surgery.
    Interactive cardiovascular and thoracic surgery, 2008, Volume: 7, Issue:3

    Topics: Abdominal Wall; Acidosis, Lactic; Biomarkers; Child, Preschool; Epinephrine; Feasibility Studies; Fo

2008
Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency.
    Pediatric neurology, 1994, Volume: 11, Issue:3

    Topics: Acidosis, Lactic; Agenesis of Corpus Callosum; Brain; Brain Damage, Chronic; Brain Diseases, Metabol

1994
Determination of the anaerobic threshold by gas exchange: biochemical considerations, methodology and physiological effects.
    Zeitschrift fur Kardiologie, 1994, Volume: 83 Suppl 3

    Topics: Acid-Base Equilibrium; Acidosis, Lactic; Adult; Anaerobic Threshold; Bicarbonates; Carbon Dioxide; E

1994
Lactated Ringer's solution alleviates brain trauma-precipitated lactic acidosis in hemorrhagic shock.
    Journal of neurotrauma, 1993,Fall, Volume: 10, Issue:3

    Topics: Acidosis, Lactic; Animals; Blood Glucose; Brain Injuries; Cerebral Hemorrhage; Gases; Hydrogen-Ion C

1993
[Effects of steroids on hepatic ATP and L/P ratio in rats subjected to acute hemorrhage].
    Masui. The Japanese journal of anesthesiology, 1997, Volume: 46, Issue:5

    Topics: Acidosis, Lactic; Acute Disease; Adenosine Triphosphate; Animals; Anti-Inflammatory Agents; Glycogen

1997
Evolution of lactate/pyruvate and arterial ketone body ratios in the early course of catecholamine-treated septic shock.
    Critical care medicine, 2000, Volume: 28, Issue:1

    Topics: Acidosis, Lactic; Adult; Aged; Aged, 80 and over; Case-Control Studies; Catecholamines; Female; Hemo

2000
Time-pattern of lactate and lactate to pyruvate ratio in the first 24 hours of intensive care emergency admissions.
    Shock (Augusta, Ga.), 2000, Volume: 14, Issue:1

    Topics: Acidosis, Lactic; APACHE; Biomarkers; Critical Care; Emergencies; Female; Finland; Glasgow Coma Scal

2000
Osmolar gap metabolic acidosis in a 60-year-old man treated for hypoxemic respiratory failure.
    Chest, 2000, Volume: 118, Issue:2

    Topics: Acidosis, Lactic; Drug Combinations; Humans; Hypnotics and Sedatives; Hypoxia; Infusions, Intravenou

2000
[An autopsy case of neonatal lactic acidosis].
    Pathologica, 2001, Volume: 93, Issue:1

    Topics: Acidosis, Lactic; Atrophy; Autopsy; Body Fluids; Brain; Cardiomegaly; Epilepsy, Generalized; Fatal O

2001
Decrease of pyruvate dehydrogenase phosphatase activity in patients with congenital lactic acidemia.
    Clinica chimica acta; international journal of clinical chemistry, 1992, Jul-31, Volume: 209, Issue:1-2

    Topics: Acidosis, Lactic; Child; Enzyme Activation; Female; Fibroblasts; Humans; Infant; Male; Mitochondria;

1992
Investigation of enzyme defects in children with lactic acidosis.
    Journal of inherited metabolic disease, 1992, Volume: 15, Issue:5

    Topics: Acidosis, Lactic; Body Fluids; Child; Citrate (si)-Synthase; Electron Transport Complex IV; Fibrobla

1992
Is the anaerobic threshold truly anaerobic?
    Chest, 1992, Volume: 101, Issue:5 Suppl

    Topics: Acidosis, Lactic; Anaerobic Threshold; Anaerobiosis; Exercise; Exercise Test; Humans; Lactates; Lact

1992
Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis.
    The Journal of pediatrics, 1992, Volume: 121, Issue:2

    Topics: Acidosis, Lactic; Humans; Infant, Newborn; Ketoglutarate Dehydrogenase Complex; Ketone Bodies; Lacta

1992
Neonatal cardiomyopathy and lactic acidosis responsive to thiamine.
    Journal of inherited metabolic disease, 1991, Volume: 14, Issue:1

    Topics: Acidosis, Lactic; Cardiomyopathies; Carnitine; Child; Child, Preschool; Female; Humans; Infant; Keto

1991
Marked reduction in CSF lactate and pyruvate levels after CoQ therapy in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Acta neurologica Scandinavica, 1991, Volume: 83, Issue:6

    Topics: Acidosis, Lactic; Adult; Agnosia; Cerebrovascular Disorders; Delirium; Dose-Response Relationship, D

1991
Therapeutic effect of sodium dichloroacetate on visual and auditory hallucinations in a patient with MELAS.
    Neuropediatrics, 1991, Volume: 22, Issue:3

    Topics: Acidosis, Lactic; Administration, Oral; Adult; Auditory Perception; Dichloroacetic Acid; Hallucinati

1991
The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lacticacidemia.
    Pediatric research, 1990, Volume: 28, Issue:5

    Topics: Acidosis, Lactic; Brain Diseases; Cells, Cultured; Cytochrome-c Oxidase Deficiency; Fibroblasts; Hum

1990
Effect of sodium dichloroacetate on human pyruvate metabolism.
    Brain & development, 1989, Volume: 11, Issue:3

    Topics: Acetates; Acidosis, Lactic; Adolescent; Blood Platelets; Dichloroacetic Acid; Humans; Male; Muscular

1989
Detection of pyruvate metabolism disorders by culture of skin fibroblasts with dichloroacetate.
    Pediatric research, 1988, Volume: 23, Issue:6

    Topics: Acetates; Acidosis, Lactic; Cells, Cultured; Child; Dichloroacetic Acid; Enzyme Activation; Female;

1988
Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy.
    The Journal of clinical investigation, 1987, Volume: 80, Issue:1

    Topics: Acidosis, Lactic; Bone and Bones; Brain; Electron Transport; Energy Metabolism; Humans; Infant, Newb

1987
Fatal lactic acidosis due to deficiency of E1 component of the pyruvate dehydrogenase complex.
    Journal of inherited metabolic disease, 1988, Volume: 11, Issue:2

    Topics: Acidosis, Lactic; Humans; Infant; Male; Oxidation-Reduction; Pyruvate Dehydrogenase Complex; Pyruvat

1988
[Congenital lactic acidemia].
    Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 1988, Volume: 33, Issue:5

    Topics: Acidosis, Lactic; Biological Transport; Energy Metabolism; Humans; Mitochondria; NAD; Pyruvate Dehyd

1988
Renal effects of dichloroacetate in vivo.
    Clinica chimica acta; international journal of clinical chemistry, 1986, Nov-15, Volume: 160, Issue:3

    Topics: Acetates; Acidosis, Lactic; Administration, Oral; Child, Preschool; Dichloroacetic Acid; Gas Chromat

1986