期刊论文详细信息
BMC Complementary and Alternative Medicine
Solenostemon monostachyus, Ipomoea involucrata and Carica papaya seed oil versus Glutathione, or Vernonia amygdalina: Methanolic extracts of novel plants for the management of sickle cell anemia disease
Bosede Temitope Adekeye1  Alaba O Adeyemi1  Tolulope Bisi-Adeniyi1  Damilola Olufunlayo Ogunleye1  Priscilla Ibanga Usoro1  Oluwabukunmi Dorcas Fajimi1  Iyanuoluwa Olubukola Osikoya1  Israel Sunmola Afolabi1 
[1] Biological Sciences Department, Covenant University, College of Science and Technology, Biochemistry Unit, Canaan Land, Km. 10, Idiroko Road, P.M.B. 1023, Ota, Ogun State, Nigeria
关键词: Plants;    Underutilized;    Antisickling;    Management;    Health;    Sickle cell disease;   
Others  :  1231304
DOI  :  10.1186/1472-6882-12-262
 received in 2012-07-19, accepted in 2012-12-18,  发布年份 2012
PDF
【 摘 要 】

Background

Sickle cell disease (SCD) is a genetic disease caused by an individual inheriting an allele for sickle cell hemoglobin from both parents and is associated with unusually large numbers of immature blood cells, containing many long, thin, crescent-shaped erythrocytes. It is a disease prevalent throughout many populations. The use of medicinal plants and nutrition in managing SCD is gaining increasing attention.

Methods

The antisickling effects of Solenostemon monostachyus (SolMon), Carica papaya seed oil (Cari-oil) and Ipomoea involucrata (Ipocrata) in male (HbSSM) and female (HbSSF) human sickle cell blood was examined in vitro and compared with controls, or cells treated with glutathione or an antisickling plant (Vernonia amygdalina; VerMyg).

Results

Levels of sickle blood cells were significantly reduced (P < 0.05) in all the plant-extract treated SCD patients’ blood compared with that of untreated SCD patients. RBCs in SolMon, Ipocrata, and Cari-oil treated samples were significantly higher (P < 0.05) compared with VerMyg-treated samples. The Fe2+/Fe3+ ratio was significantly reduced (P < 0.05) in all plant extract-treated HbSSM samples compared with controls. Hemoglobin concentration was significantly increased (P < 0.05) by SolMon treatment in HbSSF compared with VerMyg. Sickle cell polymerization inhibition exhibited by SolMon was significantly higher (P < 0.05) compared with that of VerMyg in HbSSF blood. Sickle cell polymerization inhibition in SolMon and Ipocrata were significantly higher (P < 0.05) compared with VerMyg in HbSSM blood. All plant extracts significantly reduced (P < 0.05) lactate dehydrogenase activity in both HbSSM and HbSSF-treated blood. Catalase activity was significantly increased (P < 0.05) in HbSSF blood treated with Ipocrata compared with glutathione. Cari-oil treated HbSSM and HbSSF blood had significantly increased (P < 0.05) peroxidase activity compared with controls.

Conclusions

Methanolic extracts from S. monostachyus, C. papaya seed oil and I. involucrata exhibited particular antisickling properties coupled with the potential to reduce stress in sickle cell patients. Each plant individually or in combination may be useful for the management of sickle cell disease.

【 授权许可】

   
2012 Afolabi et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20151109095700204.pdf 639KB PDF download
Figure 5. 32KB Image download
Figure 4. 33KB Image download
Figure 3. 35KB Image download
Figure 2. 29KB Image download
Figure 1. 38KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

Figure 5.

【 参考文献 】
  • [1]Okpuzor J, Adebesin O, Ogbunugafor H, Amadi I: The potential of medicinal plants in sickle cell disease control: a review. Int J Biomed Health Sci 2008, 4(2):47-55.
  • [2]WHO: Guidelines on developing consumer on proper use of traditional, complementary and alternative medicine. In The report of WHO Consultation on Proper Use of Traditional Medicine and Complementary Medicine by Consumers held at Milan, Italy, 1–3 December 2003. Edited by WHO, vol. 1, First edn. Milan (Italy). 1st edition. Milan (Italy): World Health Organisation (WHO); 2004:87.
  • [3]Elujoba AA, Odeleye OM, Ogunyemi CM: Traditional medicine development for medical and dental primary health care delivery system in Africa. Afr J Tradit Complement Altern Med 2005, 2:46-61.
  • [4]Dapa D, Gil T: Sickle cell disease in Africa. Curr Opinin Haematol 2002, 9:111-116.
  • [5]Mpiana PT, Ngbolua KN, Mudogo V, Tshibangu DST, Atibu EK, Tshilanda DD, Misengabu NM: Anti sickle erythrocytes haemolysis properties and inhibitory effect of anthocyanins extracts of Trema orientalis (Ulmaceae) on the aggregation of human deoxyhemoglobin S in vitro. J Med Sci 2011, 11:129-137.
  • [6]Iyamu EW, Ernest A, Toshio A: Niprisan (Nix-0699) improves the survival rates of transgenic sickle cell mice under acute severe hypoxic conditions. Br J Haematol 2003, 122:1001-1008.
  • [7]Brugnara C, De Franceshi L, Alper SL: Inhibition of Ca2+ dependent K+ transport and cell dehydration in sickle erythryocytes by CLT and other imidazole derivatives. J Clin Invest 1993, 92:520-526.
  • [8]Ekeke GI, Uwakwe AA, Nwaoguikpe R: The action of ripe fruit juices on hemoglobin polymerization, Fe2+/Fe3+ ratio and lactate dehydrogenase activity of sickle cell (HbSS) blood. Nig J Biochem Mol Biol 2001, 16(1):31-35.
  • [9]Nwaoguikpe RN, Braide W: Some fruit juices as environmental sickling agents. World J Med Sci 2010, 5:98-104.
  • [10]Nwaoguike RN, Uwakwe AA: The antisickling effects of dried fish (tilapia) and dried prawn (Astacus red). J Appl Sci Environ Manage 2005, 9:115-119.
  • [11]Afolabi IS, Akuiyibo SM, Rotimi SO, Adeyemi AO: In vivo evaluation of lipid and antioxidants qualities of Carica papaya seed oil. J Nat Prod 2011, 4:125-135.
  • [12]Afolabi IS, Ofobrukweta K: Physicochemical and nutritional qualities of Carica papaya seed products. JMPR 2011, 5(14):3115-3117.
  • [13]Okoko T, Ere D: Antioxidant activities of Solenostemon monostachyus leaf extract using in vitro methods. Sci Res Assays 2012, 7:621.
  • [14]Yeap SK, Ho WY, Beh BK, Liang WS, Ky H, Yousr AHN, Alitheen NB: Vernonia amygdalina, an ethnoveterinary and ethnomedical used green vegetable with multiple bioactivities. JMPR 2010, 4(25):2787-2812.
  • [15]Ogunyemi CM, Elujoba AA, Durosinmi MA: Antisickling properties of Carica papaya Linn. J Nat Prod 2008, 1:56-66.
  • [16]Sinha KA: Colorimetric assay of Catalase. Anal Biochem 1972, 47:389-394.
  • [17]Wever R, Hamers M, Weening R, Roos D: Characterization of the peroxidase in human eosinophils. Eur J Biochem 1980, 108:491-505.
  • [18]Garner C, Tatu T, Reittie JE, Littlewood T, Darley J, Cervino S, Farrall M, Kelly P, Spector TD, Thein SL: Genetic influences on F cells and other hematologic variables: a twin heritability study. Blood 2000, 95(1):342-346.
  • [19]Akinnuga AM, Bamidele O, Chukwuebuka IC: Correlation between packed cell volume and body mass index in hypertensive and normotensive subjects. Ann Biol Res 2011, 2(2):65-71.
  • [20]Tirlapur VG, Gicheru K, Charalambous BM, Evans PJ, Mir MA: Packed cell volume, haemoglobin, and oxygen saturation changes in healthy smokers and non-smokers. Thorax 1983, 38:785-787.
  • [21]McCurdy PR, Mahmood L, Sherman AS: Red cell life span in sickle cell-hemoglobin C disease with a note about sickle cell-hemoglobin O ARAB. Blood 1975, 45:273-279.
  • [22]Milner PF, Charache S: Life span of carbamylated red cells in sickle cell anemia. J Clin Invest 1973, 52(12):3161-3171.
  • [23]Shimizu H, Tamam M, Soemantri A, Ishida T: Glucose-6-phosphate dehydrogenase deficiency and Southeast Asian ovalocytosis in asymptomatic plasmodium carriers in Sumba island, Indonesia. J Hum Genet 2005, 50:420-424.
  • [24]Ferreira A, Marguti I, Bechmann I, Jeney V, Chora Â, Palha NR, Rebelo S, Henri A, Beuzard Y, Soares MP: Sickle hemoglobin confers tolerance to plasmodium infection. Cell 2011, 145(3):398-409.
  • [25]Simpore J, Liboudo D, Damintoti K, Sawadogo L, Maria E, Binet S, Nitiema H, Ouedraogo P, Pignatelli S, Nikiema J: Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Burkina Faso. Pak J Biol Sci 2007, 10:409-414.
  • [26]Ekpenyong EA, Eyo JE: Malaria control and treatment strategies among school children in semi-urban tropical communities. West Indian Med J 2008, 57(5):456-461.
  • [27]Yeshiwondim AK, Gopal S, Hailemariam AT, Dengela DO, Patel HP: Spatial analysis of malaria incidence at the village level in areas with unstable transmission in Ethiopia. Int J Health Geogr 2009, 8:5. BioMed Central Full Text
  • [28]Ayele DG, Zewotir TT, Mwambi HG: Prevalence and risk factors of malaria in Ethiopia. Malar J 2012, 11:195. BioMed Central Full Text
  • [29]Capellini MD, Fiorelli G: Glucose-6-phosphate dehydrogenase deficiency. Lancet 2008, 371:64-65.
  • [30]Manganelli G, Fico A, Martini G, Filosa S: Discussion on pharmacogenetic interaction in G6PD deficiency and methods to identify potential hemolytic drugs. Cardiovasc Hematol Disord Drug Targets 2010, 10:143.
  • [31]Osuagwu CG: Mechanism of the antisickling effects of Cajanus cajan and phenylalanine. Nig J Biochem Mol Biol 2010, 25:68-71.
  • [32]Nwaoguikpe RN, Ejele EA: Amino acid profile of some anti-sickling plant extracts and their haemoglobin polymerization inhibition. Nig J Biochem Mol Biol 2010, 25(2):53-59.
  • [33]Diamantino T, Amadeu E, Soaresa M, Guilherminoc L: Lactate dehydrogenase activity as an effect criterion in toxicity tests with Daphnia magna Straus. Chemosphere 2001, 45:553-560.
  • [34]Hamadah K, Basiouny A, Ghoneim KS: Alterations in the lactate dehydrogenase activity of the desert locust Schistocerca gregaria by the wild plant Fagonia bruguieri (Zygophyllaceae). Egypt Acad J Biol Sci 2010, 3:1-9.
  • [35]Lin JP, Zheng G, Joo J, Cupples LA: Genome-wide linkage and association scans for quantitative trait loci of serum lactate dehydrogenase—The framingham heart study. Hum Genom Proteomics 2010, 2010(Article ID 905237):1-5.
  • [36]Al-Jaleel AA-RA, Hussain MK, AL-Fadal SZS: The effect of sex and BMI on the reference values of serum LDH and ACP activities. Kufa Med J 2009, 12(2):143-148.
  • [37]Manca P, Chisu V: Testosterone attenuates morpho-functional alterations by 2-methoxyastradiol exposure and induces differentiation in C6 cells. J Cell Physiol 2011, 226:1510-1518.
  • [38]Qujeq D, Rezvani T: Catalase (antioxidant enzyme) activity in streptozotocin-induced diabetic rats. Int J Diabetes Metabol 2007, 15:22-24.
  • [39]Barp J, Araújo ASR, Fernandes TRG, Rigatto KV, Llesuy S, Belló-Klein A, Singal P: Myocardial antioxidant and oxidative stress changes due to sex hormones. Braz J Med Biol Res 2002, 35:1075-1081.
  • [40]Syed DN, Mukhtar H: Gender bias in skin cancer: role of catalase revealed. J Invest Dermatol 2012, 132:512-514.
  • [41]Dhahbi JM, Tillman JB, Cao S, Mote PL, Walford RL, Spindler SR: Caloric intake alters the efficiency of catalase mRNA translation in the liver of old female mice. J Gerontol Ser A 1998, 53A(3):B180-B185.
  • [42]Al-Abrash A, Al-Quobaili A, Al-Akhras G: Catalase evaluation in different human diseases associated with oxidative. Saudi Med J 2000, 21(9):827.
  • [43]Milton N: Homocysteine Inhibits Hydrogen Peroxide Breakdown by Catalase. Open Enzym Inhib J 2008, 1:34-41.
  • [44]Kapralov A, Vlasova II, Feng W, Maeda A, Walson K, Tyurin VA, Huang Z, Aneja RK, Carcillo J, Bayır H, et al.: Peroxidase activity of hemoglobin-haptoglobin complexes. covalent aggregation and oxidative stress in plasma and macrophages. J Biol Chem 2009, 284(44):30395-30407.
  文献评价指标  
  下载次数:140次 浏览次数:125次