Published October 20, 2022 | Version v1

HUMAN IMMUNODEFICIENCY VIRUS (HIV-1) REVERSE RANSCRIPTASE INHIBITORYACTIVITY OF ECLIPTA ALBA (L) LEAVES CRUDE EXTRACTS

  • 1. Infectious Diseases & Metabolic Disorders Research Lab, Department of Zoology, Kakatiya University, Warangal-506009, (A.P), India.

Description

ABSTRACT

Highly active anti-retroviral therapy (HAART) is the current HIV/AIDS treatment modality. Despite the fact that HAART is very effective in suppressing HIV-1 replication and reducing the mortality of HIV/AIDS patients, it has become increasingly clear that HAART does not offer an ultimate cure to HIV/AIDS. The high cost of the HAART regimen has impeded its delivery to over 90% of the HIV/AIDS population in the world. This reality has urgently called for the need to develop inexpensive alternative anti-HIV/AIDS therapy. This need has further manifested by recent clinical trial failures in anti-HIV-1 vaccines and microbicides.  In the current study, we characterized a panel of extracts of traditional medicinal plants for their activities against HIV-1 replication. The aim of the present study was to evaluate the in vitro anti- HIV activity of Eclipta alba plant extracts. Extracts were prepared from dried leaves in Hexane, Chloroform, Ethyl acetate, Acetone and Methanol. Peripheral Blood Mononuclear Cells (PBMCs) isolated from healthy donors by ficoll-hypaque density gradient centrifugation method. A toxicity study was performed on all crude extracts by MTT assay using PBMCs isolated from whole blood. HIV-1 RT inhibition activity of the all solvent extracts of Eclipta alba was determined by a RetrsoSys HIV-1 RT activity kit (Innovagen,Sweden). The aerial parts of Eclipta alba extracts are shows anti-HIV-1 activity and this plant has great potential for developing useful drugs.

Key words: HIV, Eclipta alba, PBMCs, HIV-1 RT, Cytotoxicity..

REFERENCES

  1. Brown, P., Gibbs Jr., C.J., Rodgers-Johnson, P., Asher, D.M., Sulima, M.P., Bacote, A. &Gajdusek, D.C. 2004. Human spongiform encephalopathy: The National Institute of Health series of 300 cases of experimentally transmitted disease. Annals of Neurology35. 513-529.
  2. Budka, H., Aguzzi, A., Brown, P., Brucher, J.M,Bugiani, O., Collinge, J., Diringer, H.,Gullotta, F., Haltia, M. &Hauw, J.J. 1995. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (priondiseases).Brain Pathology 5, 319-322.
  3. Cowan, M.M. 1999. Plant products a antimicrobial agents. Clinical Microbiology Reviews 12, 564-582.
  4. King, H., &Rewers, M. 1993. Global estimates for prevalence of diabetes mellitus and impaired glucose tolerance in adults. WHOAd Hoc Diabetes Reporting Group. Diabetes Care 16, 157-177.
  5. Van Everbroeck, B., Pals, P., Dziedzie, T., Dom, R.,Godfraind, C., Sciot, R., Brucher, J.M.,Martin, J.J. &Cras, P. 2000. Retrospective study of Creutzfeldt-Jakob disease inBelgium: europhysiological findings. ActaNeoropathologica(Berl) 99, 358-364.
  6. Vermani K, Garg S 2002. Herbal medicines for sexually transmitted diseases and AIDS. J. Ethnopharmacol.,80: 49–66.

Files

000n.pdf

Files (607.9 kB)

Name Size
md5:6036682dcca9605c6b88ab98e58280ab
607.9 kB Preview Download