Antiplasmodial, Antioxidant and Cytotoxicity Activity of Ethanol and Aqueous Extracts of Khaya grandifoliola Stem Bark

被引:4
作者
Guy-Armand, Gamago Nkadeu [1 ]
Cedric, Yamssi [2 ]
Nadia, Noumedem Anangmo Christelle [3 ]
Azizi, Mounvera Abdel [1 ]
Sidiki, Ngouyamsa Nsapkain Aboubakar [1 ]
Sandra, Tientcheu Noutong Jemimah [1 ]
Kevin, Tako Djimefo Alex [4 ]
Payne, Vincent Khan [1 ]
机构
[1] Univ Dschang, Fac Sci, Dept Anim Biol, POB 067, Dschang, Cameroon
[2] Univ Bamenda, Fac Hlth Sci, Dept Biomed Sci, POB 39, Bambili, Cameroon
[3] Univ Dschang, Fac Med & Pharmaceut Sci, Dept Microbiol Hematol & Immunol, POB 96, Dschang, Cameroon
[4] Univ Douala, Fac Sci, Dept Anim Organisms, POB 24157, Douala, Cameroon
关键词
IN-VITRO; ANTIMALARIAL ACTIVITY; VIVO;
D O I
10.1155/2023/8062453
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background. Malaria is a serious public health problem, especially in sub-Saharan Africa. The aim of this study was to scientifically provide baseline information on the use of Khaya grandifoliola stem bark as an antimalaria drug by traditional healers. Method. The stem barks of K.grandifoliola were harvested and dried to obtain powder, and fifty grams of the powder were soaked in ethanol and hot distilled water respectively, for the preparation of ethanol and aqueous extracts, then dried in an oven at 40 degrees C for the ethanol extract and 50 degrees C for the aqueous extract. Plasmodium falciparum strains 3D7 sensitive and Dd2 resistant to chloroquine, were used to evaluate in vitro antiplasmodial activity using SYBR Green. The ability of the extracts to prevent oxidative stress was assessed by trapping 2, 2 '-diphenyl-1-picrylhydrazyl (DPPH); nitric oxide, hydrogen peroxide and ferric reducing power. The cytotoxicity test of the extracts was carried out on RAW 264.7 cell lines and on erythrocytes. The data obtained were entered in the Excel software, then in Graph pad where the IC50 was calculated and the curves plotted. Results. The fifty percent inhibition (IC50) of the antiplasmodial activity of the chloroquine-resistant strain PfDd2 were 54.27 +/- 2.41 mu g/mL and 31.19 +/- 4.06 mu g/mL respectively, for the aqueous and ethanol extracts. As for the Chloroquino-sensitive Pf3D7, IC50 of 53.06 mu g/mL was obtained for the aqueous extract and 28.03 +/- 1.90 mu g/mL for ethanol. The DPPH radical scavenging activity presented IC50 of 104 mu g/mL for the aqueous and 2.617 mu g/mL for the ethanol extract; for the Nitric oxide (NO) presented an IC50 of 301 +/- 21 mu g/mL for the aqueous extract 140.7 +/- 21 mu g/mL for the ethanol; for hydrogen peroxide the ethanol and aqueous presented IC50 of 845.1 +/- 21 mu g/mL and 509.4 +/- 21 mu g/mL respectively. The cytotoxicity on RAW 264.7 cells presented High CC50 in particular >1000 mu g/mL and 467.4 mu g/mL respectively for the aqueous and ethanol extract. Conclusion. Extracts of Khaya grandifoliola exhibited antiplasmodial activity. The ability to inhibit oxidative stress as well as lower cell toxicity on RAW 264.7 and erythrocytes, is a good indicator. However, in vivo tests remain important in order to confirm the use of this plant for the treatment of malaria.
引用
收藏
页数:8
相关论文
共 42 条
  • [21] In vitro cytotoxic activity of Thai medicinal plants used traditionally to treat cancer
    Itharat, A
    Houghton, PJ
    Eno-Amooquaye, E
    Burke, PJ
    Sampson, JH
    Raman, A
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2004, 90 (01) : 33 - 38
  • [22] Cytotoxic, anti-inflammatory and antioxidant activities of four different extracts of Galega officinalis L (Goat's rue)
    Karakas, Fatma Pehlivan
    Turker, Arzu Ucar
    Karakas, Alper
    Mshvildadze, Vakhtang
    [J]. TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH, 2016, 15 (04) : 751 - 757
  • [23] Kodjio N., 2020, PHYTOCHEM LETT, V9
  • [24] Kumar G., 2011, Elixir Appl Botany, V40, pe5537
  • [25] Kumari D., 2016, WORLD J PHARM SCI, V4, P495
  • [26] Makinde J. M., 1988, PHYTOTHER RES, V2, P30, DOI [10.1002/ptr.2650020104, DOI 10.1002/PTR.2650020104]
  • [27] Mfopa A. N., 2017, International Journal of Biological and Chemical Sciences, V11, P118, DOI 10.4314/ijbcs.v11i1.10
  • [28] Nadia N. A. C., 2017, Euro. J Med. Plants, V21, P1, DOI [10.9734/EJMP/2017/36352, DOI 10.9734/EJMP/2017/36352]
  • [29] Nnanga N., 2020, HLTH SCI DIS, V21
  • [30] Odugbemi TO, 2007, AFR J TRADIT COMPLEM, V4, P191