Tekleab Teka Teklehaimanot

Mr. Tekleab Teka Teklehaimanot


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2021 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
HZHan Zhang
Han Zhang
XWXiaoming Wang
Xiaoming Wang
YGYaqing Guo
Yaqing Guo
XLXiaomei Liu
Xiaomei Liu
XZXizi Zhao
Xizi Zhao
GPGuixiang Pan
Guixiang Pan

28 October 2016 in Molecules
Verified
Journal Article
Open access
PDF file
TTTekleab Teka Teklehaimanot
Tekleab Teka Teklehaimanot
DBDaniel Bistrat
Daniel Bistrat
MYMariamawit Yonathan Yeshak
Mariamawit Yonathan Yeshak
KAKaleab Asres
Kaleab Asres
Malaria is one of the three major global public health threats due to a wide spread resistance of the parasites to the standard antimalarial drugs. Considering this growing problem, the ethnomedicinal approach in the search for new antimalarial drugs from plant sources has proven to be more effective and inexpensive. The leaves of Aloe pulcherrima Gilbert and Sebsebe, an endemic Ethiopian plant, are locally used for the treatment of malaria and other infectious diseases. Application of the leaf latex of A. pulcherrima on preparative silica gel TLC led to the isolation of two C-glycosylated anthrones, identified as nataloin (1) and 7-hydroxyaloin (2) by spectroscopic techniques (UV, IR, 1H- and 13C-NMR, HR-ESIMS). Both the latex and isolated compounds displayed antimalarial activity in a dose-independent manner using a four-day suppressive test, with the highest percent suppression of 56.2% achieved at 200 mg/kg/day for 2. The results indicate that both the leaf latex of A. pulcherrima and its two major constituents are endowed with antiplasmodial activities, which support the traditional use of the leaves of the plant for the treatment of malaria.

1 October 2021 in Journal of Pharmaceutical and Biomedical Analysis
Verified
Journal Article
Closed access
YXYanchao Xing
Yanchao Xing
ZYZhe Yan
Zhe Yan
YLYuhong Li
Yuhong Li
TTTekleab Teka Teklehaimanot
Tekleab Teka Teklehaimanot
GPGuixiang Pan
Guixiang Pan
LHLifeng Han
Lifeng Han

1 November 2021 in Journal of Pharmaceutical and Biomedical Analysis
Verified
Journal Article
Closed access
WHWenwen Huang
Wenwen Huang
ZZZhonglian Zhang
Zhonglian Zhang
LNLu Niu
Lu Niu
XHXiaohan Hu
Xiaohan Hu
TTTekleab Teka Teklehaimanot
Tekleab Teka Teklehaimanot
QWQilong Wang
Qilong Wang

2 January 2019 in International Journal of Microbiology
Verified
Journal Article
Open access
PDF file
YEYohannes Kelifa Emiru
Yohannes Kelifa Emiru
ESEbrahim Abdela Siraj
Ebrahim Abdela Siraj
TTTekleab Teka Teklehaimanot
Tekleab Teka Teklehaimanot
GAGedefaw Getnet Amare
Gedefaw Getnet Amare
Objective. To evaluate the antibacterial effects of the leaf latex of Aloe weloensis against infectious bacterial strains. Methods. The leaf latex of A. weloensis at different concentrations (400, 500, and 600 mg/ml) was evaluated for antibacterial activities using the disc diffusion method against some Gram-negative species such as Escherichia coli (ATCC 14700) and Pseudomonas aeruginosa (ATCC 35619) and Gram-positive such as Staphylococcus aureus (ATCC 50080) and Enterococcus fecalis (ATCC 4623). Results. The tested concentrations of the latex ranging between 400 and 600 mg·mL−1 showed significant antibacterial activity against bacterial strain. The highest dose (600 mg/ml) of A. weloensis leaf latex revealed the maximum activity (25.93 ± 0.066 inhibition zone) followed by the dose 500 mg/ml against S. aureus. The lowest antibacterial activity was observed by the concentration 400 mg/ml (5.03 ± 0.03) against E. coli. Conclusion. The results of the present investigation suggest that the leaf latex of A. weloensis can be used as potential leads to discover new drugs to control some bacterial infections.

21 June 2021 in Journal of Tropical Medicine
Verified
Journal Article
Open access
PDF file
GGGebrehiwot Kiros Gebremariam
Gebrehiwot Kiros Gebremariam
HKHaile Kassahun
Haile Kassahun
TTTekleab Teka Teklehaimanot
Tekleab Teka Teklehaimanot
TGTsgab Gebrecherkos Girmay
Tsgab Gebrecherkos Girmay
Background. Malaria is a major health concern in the world in general and developing countries in particular. Nowadays, the control of malaria has ended up steadily more complex due to the spread of drug-resistant parasites. Medicinal plants are the verifiable source of compelling antimalarial drugs. The present study was aimed to assess the in vivo antimalarial activity of leaf latex of A. melanacantha against Plasmodium berghei in mice. Methods. Acute oral toxicity study of the leaf latex was assessed in mice up to a dose of 2,000 mg/kg. A four-day suppressive model was utilized to investigate the antimalarial activity of the plant. Three extract doses, 100, 200, and 400 mg/kg/day, doses of the plant leaf latex, chloroquine, 10 mg/kg (positive control) and distilled water, and 10 mL/kg (negative control) were administered to mice. Percent parasitemia suppression, packed cell volume, mean survival time, body weight, and rectal body temperature were used to determine antimalarial activity. Results. Test groups treated with 100, 200, and 400 mg/kg of the latex showed a significant parasitemia suppression in dose dependent manner compared to the negative control with an IC50 of 22.63 mg/ml. Mice treated with 100, 200, and 400 mg/kg have shown parasitemia suppression of 14.86%, 29%, and 43.2%, respectively. The chemosuppression was significant ( ) at all doses compared to the negative control. Similarly, mice treated with 100 mg/kg, 200 mg/kg, and 400 mg/kg have shown a significant survival time compared to the negative control. At the same time, weight loss reduction was observed within the test groups treated with 100 mg/kg and 200 mg/kg of the latex while the test groups treated with 400 mg/kg had showed almost no weight loss reduction. The latex also reversed the PCV reduction significantly ( ) at 200 mg/kg and 400 mg/kg doses and prevented rectal temperature dropping significantly ( ) at all doses. Conclusion. The leaf latex of A. melanacantha has shown significant antimalarial activity against P. berghei in mice supporting the genuine traditional antimalarial usage of the plant.