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butyric acid and Anemia, Sickle Cell

butyric acid has been researched along with Anemia, Sickle Cell in 15 studies

Butyric Acid: A four carbon acid, CH3CH2CH2COOH, with an unpleasant odor that occurs in butter and animal fat as the glycerol ester.
butyrate : A short-chain fatty acid anion that is the conjugate base of butyric acid, obtained by deprotonation of the carboxy group.
butyric acid : A straight-chain saturated fatty acid that is butane in which one of the terminal methyl groups has been oxidised to a carboxy group.

Anemia, Sickle Cell: A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.

Research Excerpts

ExcerptRelevanceReference
" The fact that valproic acid, a derivative of pentanoic acid, also induces gamma-globin expression suggests that short-chain fatty acid derivatives that are already approved for human use may possess the property of gamma-globin inducibility and may be of therapeutic relevance to the beta-chain hemoglobinopathies."3.69Stimulation of fetal hemoglobin production by short chain fatty acids. ( Blau, CA; Dover, G; Fournarakis, B; Josephson, B; Li, Q; Liakopoulou, E; Papayannopoulou, T; Raisys, V; Stamatoyannopoulos, G; Wolf, JA, 1995)
" Because butyrate and alpha-amino-n-butyric acid (ABA) augment gamma globin expression in normal neonatal and adult erythroid progenitors, we investigated the effects of sodium butyrate and ABA on erythroid progenitors of patients with beta thalassemia and sickle cell anemia who might benefit from such an effect."3.67Sodium butyrate enhances fetal globin gene expression in erythroid progenitors of patients with Hb SS and beta thalassemia. ( Cohen, RA; Faller, DV; Hurst, D; Lubin, BH; Miller, BA; Papayannopoulou, T; Perrine, SP; Vichinsky, EP, 1989)
" However, application of these drugs at large is not yet justified because a series of questions concerning their long-term efficacy, the correct dosage and timing, their tolerance and toxicity, and the potential long-term dangers, including mutagenicity are still unresolved."2.40New therapies for the haemoglobinopathies. ( Loukopoulos, D, 1997)
"Only hydroxyurea has shown significant clinical effects in terms of reduction of pain-crises, chest syndrome and transfusions in sickle-cell patients."2.40Pharmacological induction of foetal haemoglobin synthesis in sickle-cell disease. ( Hillen, HF; Saleh, AW, 1997)
"Hydroxyurea (HU) has become the most widely used agent, although its effectiveness in increasing HbF levels and the number of F cells is highly variable."2.38Fetal hemoglobin reactivation in baboon and man: a short perspective. ( DeSimone, J; Heller, P; Lavelle, D, 1993)
"The pathophysiology of sickle cell anemia is primarily explained in terms of the oxygen-dependent polymerization of sickle hemoglobin (HbS) followed by sickling of erythrocytes."1.30Sickling of nucleated erythroid precursors from patients with sickle cell anemia. ( Blanchette-Mackie, EJ; Dwyer, N; Fibach, E; Hasegawa, S; Noguchi, CT; Rodgers, GP; Schechter, AN; Uyesaka, N, 1998)

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19902 (13.33)18.7374
1990's8 (53.33)18.2507
2000's0 (0.00)29.6817
2010's5 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Li, H1
Xie, W1
Gore, ER1
Montoute, MN1
Bee, WT1
Zappacosta, F1
Zeng, X1
Wu, Z1
Kallal, L1
Ames, RS1
Pope, AJ1
Benowitz, A1
Erickson-Miller, CL1
Ronzoni, L1
Sonzogni, L1
Fossati, G1
Modena, D1
Trombetta, E1
Porretti, L1
Cappellini, MD1
Fard, AD1
Kaviani, S1
Noruzinia, M1
Saki, N1
Mortaz, E1
Chou, YC1
Chen, RL1
Lai, ZS1
Song, JS1
Chao, YS1
Shen, CK1
Durlak, M1
Fugazza, C1
Elangovan, S1
Marini, MG1
Marongiu, MF1
Moi, P1
Fraietta, I1
Cappella, P1
Barbarani, G1
Font-Monclus, I1
Mauri, M1
Ottolenghi, S1
Gasparri, F1
Ronchi, A1
Liakopoulou, E1
Blau, CA1
Li, Q1
Josephson, B1
Wolf, JA1
Fournarakis, B1
Raisys, V1
Dover, G1
Papayannopoulou, T2
Stamatoyannopoulos, G1
Lavelle, D1
DeSimone, J1
Heller, P1
Fibach, E2
Prasanna, P1
Rodgers, GP2
Samid, D1
Loukopoulos, D1
Faller, DV4
Perrine, SP4
Saleh, AW1
Hillen, HF1
Hasegawa, S1
Dwyer, N1
Noguchi, CT1
Blanchette-Mackie, EJ1
Uyesaka, N1
Schechter, AN1
Swerdlow, P2
Miller, BA2
Bank, A1
Sytkowski, AJ1
Reczek, J2
Rudolph, AM2
Kan, YW2
Cohen, RA1
Vichinsky, EP1
Hurst, D1
Lubin, BH1
Qin, G1

Reviews

5 reviews available for butyric acid and Anemia, Sickle Cell

ArticleYear
Induction of fetal hemoglobin as a novel therapeutic strategy for β-hemoglobinopathy.
    Laboratory hematology : official publication of the International Society for Laboratory Hematology, 2014, Mar-01, Volume: 20, Issue:1

    Topics: Anemia, Sickle Cell; Angiogenesis Inhibitors; Animals; beta-Thalassemia; Butyric Acid; Drug Synergis

2014
Fetal hemoglobin reactivation in baboon and man: a short perspective.
    American journal of hematology, 1993, Volume: 42, Issue:1

    Topics: Anemia, Sickle Cell; Animals; Azacitidine; Butyrates; Butyric Acid; Erythropoietin; Fetal Hemoglobin

1993
New therapies for the haemoglobinopathies.
    Journal of internal medicine. Supplement, 1997, Volume: 740

    Topics: Anemia, Sickle Cell; Antisickling Agents; Butyrates; Butyric Acid; Drug Therapy, Combination; Erythr

1997
Butyrate in the treatment of sickle cell disease and beta-thalassemia.
    Current opinion in hematology, 1995, Volume: 2, Issue:2

    Topics: Anemia, Sickle Cell; beta-Thalassemia; Butyrates; Butyric Acid; Forecasting; Gene Expression Regulat

1995
Pharmacological induction of foetal haemoglobin synthesis in sickle-cell disease.
    The Netherlands journal of medicine, 1997, Volume: 51, Issue:5

    Topics: Anemia, Sickle Cell; Animals; Butyrates; Butyric Acid; Erythropoietin; Fetal Hemoglobin; Humans; Hyd

1997

Other Studies

10 other studies available for butyric acid and Anemia, Sickle Cell

ArticleYear
Development of phenotypic screening assays for γ-globin induction using primary human bone marrow day 7 erythroid progenitor cells.
    Journal of biomolecular screening, 2013, Volume: 18, Issue:10

    Topics: Anemia, Sickle Cell; Azacitidine; Bone Marrow Cells; Butyric Acid; Cell Survival; Decitabine; DNA Mo

2013
Modulation of gamma globin genes expression by histone deacetylase inhibitors: an in vitro study.
    British journal of haematology, 2014, Volume: 165, Issue:5

    Topics: Adult; Anemia, Sickle Cell; Antigens, CD34; Butyric Acid; Carbamates; Cell Differentiation; Cells, C

2014
Pharmacological Induction of Human Fetal Globin Gene in Hydroxyurea-Resistant Primary Adult Erythroid Cells.
    Molecular and cellular biology, 2015, Volume: 35, Issue:14

    Topics: Adult; Anemia, Sickle Cell; Animals; Antineoplastic Agents; beta-Thalassemia; Blotting, Western; But

2015
A Novel High-Content Immunofluorescence Assay as a Tool to Identify at the Single Cell Level γ-Globin Inducing Compounds.
    PloS one, 2015, Volume: 10, Issue:10

    Topics: Anemia, Sickle Cell; beta-Globins; beta-Thalassemia; Butyric Acid; Fetal Hemoglobin; gamma-Globins;

2015
Stimulation of fetal hemoglobin production by short chain fatty acids.
    Blood, 1995, Oct-15, Volume: 86, Issue:8

    Topics: Adult; Anemia, Sickle Cell; Animals; Anticonvulsants; Butyrates; Butyric Acid; Cells, Cultured; Epil

1995
Enhanced fetal hemoglobin production by phenylacetate and 4-phenylbutyrate in erythroid precursors derived from normal donors and patients with sickle cell anemia and beta-thalassemia.
    Blood, 1993, Oct-01, Volume: 82, Issue:7

    Topics: Anemia, Sickle Cell; Azacitidine; beta-Thalassemia; Blotting, Northern; Butyrates; Butyric Acid; Cel

1993
Sickling of nucleated erythroid precursors from patients with sickle cell anemia.
    Experimental hematology, 1998, Volume: 26, Issue:4

    Topics: Anemia, Sickle Cell; Bone Marrow Cells; Butyrates; Butyric Acid; Cell Hypoxia; Cell Nucleus; Cells,

1998
Stopping the biologic clock for globin gene switching.
    Annals of the New York Academy of Sciences, 1990, Volume: 612

    Topics: Anemia, Sickle Cell; Animals; Biological Clocks; Butyrates; Butyric Acid; Cell Line; Cells, Cultured

1990
Sodium butyrate enhances fetal globin gene expression in erythroid progenitors of patients with Hb SS and beta thalassemia.
    Blood, 1989, Volume: 74, Issue:1

    Topics: Anemia, Sickle Cell; Butyrates; Butyric Acid; Cells, Cultured; Child; Child, Preschool; Erythropoies

1989
Butyric acid modulates developmental globin gene switching in man and sheep.
    Advances in experimental medicine and biology, 1989, Volume: 271

    Topics: Acetylation; Adult; Anemia, Sickle Cell; Animals; Butyrates; Butyric Acid; Fetal Hemoglobin; Gene Ex

1989