nitrites has been researched along with HbS Disease in 20 studies
Nitrites: Salts of nitrous acid or compounds containing the group NO2-. The inorganic nitrites of the type MNO2 (where M=metal) are all insoluble, except the alkali nitrites. The organic nitrites may be isomeric, but not identical with the corresponding nitro compounds. (Grant & Hackh's Chemical Dictionary, 5th ed)
Excerpt | Relevance | Reference |
---|---|---|
"Hydroxyurea (HU) has been suggested to act as a nitric oxide (NO) donor in sickle cell anemia (SCA)." | 2.87 | Hydroxyurea therapy modulates sickle cell anemia red blood cell physiology: Impact on RBC deformability, oxidative stress, nitrite levels and nitric oxide synthase signalling pathway. ( Bloch, W; Cannas, G; Collins, B; Connes, P; Fort, R; Gauthier, A; Grau, M; Guillot, N; Hot, A; Joly, P; Martin, C; Nader, E; Poutrel, S; Renoux, C; Romana, M; Thevis, M; Walpurgis, K, 2018) |
"Hydroxyurea is a relatively new treatment for sickle cell disease." | 2.42 | Nitric oxide production from hydroxyurea. ( King, SB, 2004) |
"The hypothesis of decreased nitric oxide (NO) bioavailability in sickle cell disease (SCD) proposes that multiple factors leading to decreased NO production and increased consumption contributes to vaso-occlusion, pulmonary hypertension, and pain." | 1.56 | Sickle cell disease subjects and mouse models have elevated nitrite and cGMP levels in blood compartments. ( Almeida, LEF; Darbari, DS; de Souza Batista, CM; Finkel, JC; Kamimura, S; Nettleton, MY; Quezado, ZMN; Smith, ML; Spornick, N; Wakim, P; Walek, E, 2020) |
"Sickle cell disease is caused by a mutant form of hemoglobin that polymerizes under hypoxic conditions, increasing rigidity, fragility, calcium influx-mediated dehydration, and adhesivity of red blood cells." | 1.46 | Potential therapeutic action of nitrite in sickle cell disease. ( Alexander-Miller, MA; Basu, S; Bolden, CA; Buechler, NL; Caudell, DL; Gladwin, MT; Jailwala, A; Kim, HW; Kim-Shapiro, DB; Ostrowski, D; Perlegas, A; Rahbar, E; Vachharajani, V; Wajih, N, 2017) |
"In Brazil, sickle cell anemia (SCA) is one of the most common genetic disorders." | 1.38 | Impact of β(S)-globin haplotypes on oxidative stress in patients with sickle cell anemia in steady state. ( Carvalho-dos Santos, BS; Cavalcante-Barbosa, M; da Silva-Rocha, LB; Dias-Elias, DB; Pinheiro-Gonçalves, R, 2012) |
"A hemolysis-linked subphenotype of sickle cell disease (SCD), characterized by pulmonary hypertension, stroke, priapism and leg ulcers, is associated with decreased nitric oxide bioavailability and vasculopathy." | 1.35 | Novel small molecule therapeutics for sickle cell disease: nitric oxide, carbon monoxide, nitrite, and apolipoprotein A-I. ( Kato, GJ, 2008) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 5 (25.00) | 29.6817 |
2010's | 13 (65.00) | 24.3611 |
2020's | 2 (10.00) | 2.80 |
Authors | Studies |
---|---|
Almeida, LEF | 3 |
Smith, ML | 2 |
Kamimura, S | 3 |
Vogel, S | 1 |
de Souza Batista, CM | 2 |
Quezado, ZMN | 3 |
Spornick, N | 1 |
Nettleton, MY | 1 |
Walek, E | 1 |
Finkel, JC | 1 |
Darbari, DS | 1 |
Wakim, P | 2 |
Wajih, N | 1 |
Basu, S | 1 |
Jailwala, A | 1 |
Kim, HW | 1 |
Ostrowski, D | 1 |
Perlegas, A | 1 |
Bolden, CA | 1 |
Buechler, NL | 1 |
Gladwin, MT | 2 |
Caudell, DL | 1 |
Rahbar, E | 1 |
Alexander-Miller, MA | 1 |
Vachharajani, V | 1 |
Kim-Shapiro, DB | 1 |
Wang, L | 1 |
van der Meulen, JH | 1 |
Nagaraju, K | 1 |
Quezado, M | 1 |
Nader, E | 1 |
Grau, M | 1 |
Fort, R | 1 |
Collins, B | 1 |
Cannas, G | 1 |
Gauthier, A | 1 |
Walpurgis, K | 1 |
Martin, C | 1 |
Bloch, W | 1 |
Poutrel, S | 1 |
Hot, A | 1 |
Renoux, C | 1 |
Thevis, M | 1 |
Joly, P | 1 |
Romana, M | 1 |
Guillot, N | 1 |
Connes, P | 1 |
Nishank, SS | 1 |
Singh, MP | 1 |
Yadav, R | 1 |
Gupta, RB | 1 |
Gadge, VS | 1 |
Gwal, A | 1 |
Pitanga, TN | 2 |
Oliveira, RR | 1 |
Zanette, DL | 2 |
Guarda, CC | 1 |
Santiago, RP | 2 |
Santana, SS | 2 |
Nascimento, VML | 1 |
Lima, JB | 1 |
Carvalho, GQ | 1 |
Maffili, VV | 1 |
Carvalho, MOS | 1 |
Alcântara, LCJ | 1 |
Borges, VM | 2 |
Goncalves, MS | 2 |
da Guarda, CC | 1 |
Kato, GJ | 1 |
Sullivan, KJ | 2 |
Kissoon, N | 2 |
Sandler, E | 2 |
Gauger, C | 1 |
Froyen, M | 1 |
Duckworth, L | 1 |
Brown, M | 1 |
Murphy, S | 1 |
Rusanova, I | 1 |
Escames, G | 1 |
Cossio, G | 1 |
de Borace, RG | 1 |
Moreno, B | 1 |
Chahboune, M | 1 |
López, LC | 1 |
Díez, T | 1 |
Acuña-Castroviejo, D | 1 |
Gonçalves, RP | 3 |
Elias, DB | 2 |
Magalhães, HI | 1 |
de Souza, JH | 1 |
Osei-Yeboah, CT | 1 |
Rodrigues, O | 1 |
Carvalho-dos Santos, BS | 1 |
Dias-Elias, DB | 1 |
da Silva-Rocha, LB | 1 |
Cavalcante-Barbosa, M | 1 |
Pinheiro-Gonçalves, R | 1 |
Barbosa, MC | 2 |
Rocha, LB | 1 |
Dutra, LL | 1 |
Silva, HF | 1 |
Martins, AM | 1 |
Dos Santos, TE | 1 |
de Sousa, GF | 1 |
King, SB | 1 |
Nath, KA | 1 |
Shah, V | 1 |
Haggard, JJ | 1 |
Croatt, AJ | 1 |
Smith, LA | 1 |
Hebbel, RP | 1 |
Katusic, ZS | 1 |
Duckworth, LJ | 1 |
Freeman, B | 1 |
Bayne, E | 1 |
Sylvester, JE | 1 |
Lima, JJ | 1 |
Shelhamer, JH | 1 |
Ognibene, FP | 1 |
Pease-Fye, ME | 1 |
Nichols, JS | 1 |
Link, B | 1 |
Patel, DB | 1 |
Jankowski, MA | 1 |
Pannell, LK | 1 |
Schechter, AN | 1 |
Rodgers, GP | 1 |
1 review available for nitrites and HbS Disease
Article | Year |
---|---|
Nitric oxide production from hydroxyurea.
Topics: Anemia, Sickle Cell; Free Radicals; Hemoglobins; Humans; Hydroxylamine; Hydroxyurea; Iron; Models, C | 2004 |
2 trials available for nitrites and HbS Disease
Article | Year |
---|---|
Hydroxyurea therapy modulates sickle cell anemia red blood cell physiology: Impact on RBC deformability, oxidative stress, nitrite levels and nitric oxide synthase signalling pathway.
Topics: Adult; Anemia, Sickle Cell; Erythrocyte Deformability; Erythrocytes; Female; Humans; Hydroxyurea; Ma | 2018 |
Effect of oral arginine supplementation on exhaled nitric oxide concentration in sickle cell anemia and acute chest syndrome.
Topics: Acute Chest Syndrome; Acute Disease; Administration, Oral; Adolescent; Anemia, Sickle Cell; Arginine | 2010 |
17 other studies available for nitrites and HbS Disease
Article | Year |
---|---|
Nitrite decreases sickle hemoglobin polymerization in vitro independently of methemoglobin formation.
Topics: Anemia, Sickle Cell; Animals; Hemoglobin, Sickle; Leukocytosis; Methemoglobin; Mice; Nitrites | 2023 |
Sickle cell disease subjects and mouse models have elevated nitrite and cGMP levels in blood compartments.
Topics: Adult; Anemia, Sickle Cell; Animals; Biological Availability; Cyclic GMP; Disease Models, Animal; Hu | 2020 |
Potential therapeutic action of nitrite in sickle cell disease.
Topics: Anemia, Sickle Cell; Animals; Blood Platelets; Calcium; Disease Models, Animal; Human Umbilical Vein | 2017 |
The role of nitrite in muscle function, susceptibility to contraction injury, and fatigability in sickle cell mice.
Topics: alpha-Globins; Anemia, Sickle Cell; Animals; Creatine Kinase; Female; Male; Methemoglobin; Mice, Tra | 2018 |
Endothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease patients in India.
Topics: Adolescent; Alleles; Anemia, Sickle Cell; Case-Control Studies; Gene Frequency; Genetic Predispositi | 2013 |
Sickle red cells as danger signals on proinflammatory gene expression, leukotriene B4 and interleukin-1 beta production in peripheral blood mononuclear cell.
Topics: Adolescent; Anemia, Sickle Cell; Child; Child, Preschool; Erythrocytes, Abnormal; Female; Gene Expre | 2016 |
Heme changes HIF-α, eNOS and nitrite production in HUVECs after simvastatin, HU, and ascorbic acid therapies.
Topics: Anemia, Sickle Cell; Ascorbic Acid; Cells, Cultured; Dose-Response Relationship, Drug; Heme; Human U | 2016 |
Novel small molecule therapeutics for sickle cell disease: nitric oxide, carbon monoxide, nitrite, and apolipoprotein A-I.
Topics: Analgesics; Anemia, Sickle Cell; Apolipoprotein A-I; Carbon Monoxide; Clinical Trials as Topic; Cycl | 2008 |
Oxidative stress status, clinical outcome, and β-globin gene cluster haplotypes in pediatric patients with sickle cell disease.
Topics: Adolescent; Anemia, Sickle Cell; beta-Globins; Child; Child, Preschool; Female; Fetal Hemoglobin; Gl | 2010 |
Study of correlation of nitrite levels with malonaldehyde and the prognosis of patients with sickle cell disease on hydroxyurea, Ceará-Brazil.
Topics: Adult; Anemia, Sickle Cell; Blood Transfusion; Brazil; Cohort Studies; Female; Humans; Hydroxyurea; | 2011 |
Renal status of children with sickle cell disease in Accra, Ghana.
Topics: Age Factors; Anemia, Sickle Cell; Case-Control Studies; Child; Child, Preschool; Cross-Sectional Stu | 2011 |
Impact of β(S)-globin haplotypes on oxidative stress in patients with sickle cell anemia in steady state.
Topics: Adult; Aged; Anemia, Sickle Cell; beta-Globins; Brazil; Cross-Sectional Studies; Female; Fetal Hemog | 2012 |
L-arginine as an adjuvant drug in the treatment of sickle cell anaemia.
Topics: Adjuvants, Pharmaceutic; Anemia, Sickle Cell; Arginine; Erythrocyte Indices; Humans; Nitrites; Oxida | 2013 |
The role of iron overload on oxidative stress in sickle cell anemia.
Topics: Adult; Anemia, Sickle Cell; Female; Ferritins; Humans; Iron Overload; Male; Malondialdehyde; Nitrite | 2012 |
Mechanisms of vascular instability in a transgenic mouse model of sickle cell disease.
Topics: Anemia, Sickle Cell; Animals; Aorta; Autoantibodies; Blood Pressure; Calcimycin; Cyclic GMP; Disease | 2000 |
Low exhaled nitric oxide and a polymorphism in the NOS I gene is associated with acute chest syndrome.
Topics: Acute Disease; Adolescent; Anemia, Sickle Cell; Arginine; Breath Tests; Child; Citrulline; Forced Ex | 2001 |
Nitric oxide donor properties of hydroxyurea in patients with sickle cell disease.
Topics: Adolescent; Adult; Anemia, Sickle Cell; Female; Glutathione; Hemoglobins; Humans; Hydroxyurea; Lumin | 2002 |