Antivirt ®{Al 4 (SiO 4 ) 3 + 3Mg 2 SiO 4 → 2Al 2 Mg 3 (SiO 4 ) 3 } Enhances Efficacy of Co-trimoxazole in Terminating Experimental Trypanosome Infections in Mice

α
M. C. O. Ezeibe
M. C. O. Ezeibe
σ
M. I. Ezeja
M. I. Ezeja
ρ
C. A
C. A
Ѡ
I.O. Onyeachonam
I.O. Onyeachonam
¥
M. E. Sanda
M. E. Sanda
§
I. J. Ogbonna
I. J. Ogbonna
χ
E. Kalu
E. Kalu
ν
N.U. Njoku
N.U. Njoku
Ѳ
M.I. Udobi
M.I. Udobi
α Michael Okpara University of Agriculture Michael Okpara University of Agriculture

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Antivirt ®{Al 4 (SiO 4 ) 3 + 3Mg 2 SiO 4 → 2Al 2 Mg 3 (SiO 4 ) 3 } Enhances Efficacy of Co-trimoxazole in Terminating Experimental Trypanosome Infections in Mice

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Antivirt ®{Al 4 (SiO 4 ) 3 + 3Mg 2 SiO 4 → 2Al 2 Mg 3 (SiO 4 ) 3 } Enhances Efficacy of Co-trimoxazole in Terminating Experimental Trypanosome Infections in Mice Banner

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Abstract

Both bacteria and protozoa require Folic acid for replication and Cotrimoxazole inhibits synthesis of the vitamin. For its mechanism of inhibiting Folic acid, the medicine has been in use as antibacterial drug for many decades but it is not being used to treat trypanosomosis (protozoan disease). To enhance anti-Folic acid activity of the medicine in order to improve its anti-trypanosome efficacy and make it function as new medicine for sleeping sickness (tropical disease of man and animals) it was stabilized with Antivirt® (Medicinal synthetic Aluminum-magnesium silicate). At 100 % of its antibacterial dose, Cotrimoxazole significantly reduced (P≤ 0.05) trypanosome parasitemia in mice, from 12.76±1.20 to 5. 87± 0.43. When it was stabilized with the Antivirt®, 75 % of the antibacterial dose had slight reduction (P≥ 0.05) in the trypanosome parasitemia (11.30±1.01) while the 100 % -dose achieved zero (0.00±00) trypanosome parasitemia and improved total WBC counts (immunity) from 1.50±0.16 to 2.86±0.38.

References

33 Cites in Article
  1. M Barret,R Burchmore,A Stich,J Lazzari,A Frasch,J Cazullo,S Krishna (2003). The trypanosomiases.
  2. A Rashid,K Rasheed,M Asim,A Hussain (2008). Risks of vaccination: a review.
  3. S Samdi,A Fajinmi,J Kalejaye,B Wayo,M Haruna,J Yarnap,A Usman,S Hamra,A Jijitar,R Ogunwale,R Bizi,R Ovbagbedia,J Abenga (2010). Periodic Variation in Trypanosoma Infection Rates in Trade Small Ruminants at Slaughter in Kaduna Central Abattoir.
  4. E Soulsby (1982). Helminthes, Arthropods and Protozoa of domesticated animals, 7th edition.
  5. G Urquhart,J Amour,J Duncan,A Dunn,F Jennings (2002). Application of immunity in the control of parasitic disease.
  6. J Abenga,F N; Enwozor,F Lawani,C; G; Ezebuiro,J; Sule,K David (2002). Prevalence of trypanosomosis in trade cattle at slaughter in Kaduna.
  7. B Anene,C Ogbuanya,E Mbah,R Ezeokonkwo (1999). Essais préliminaires pour tester l'efficacité de <em>Cymelarsan</em> chez des chiens et des souris infectés artificiellement par <em>Trypanosoma brucei</em> isolé de chiens au Nigeria.
  8. B Anene,R Ezeokonkwo,T Mmesirionye,J Tettey,J Brock,M Barrett,H De Koning (2006). A diminazene-resistant strain of<i>Trypanosoma brucei brucei</i>isolated from a dog is cross-resistant to pentamidine in experimentally infected albino rats.
  9. (1998). <i>Epidemiology and Control of African Trypanosomiasis. Report of a WHO Expert Committee</i>. Technical Report Series No. 739. 127 pages ISBN 92 4 120739 6. World Health Organization, Geneva 1986, SF 16..
  10. K Taylor,E Authié (2004). Pathogenesis of animal trypanosomiasis..
  11. Romanus Ezeokonkwo,I Ezeh,J Onunkwo,P Obi,I Onyenwe,W Agu (2010). Comparative haematological study of single and mixed infections of mongrel dogs with Trypanosoma congolense and Trypanosoma brucei brucei.
  12. R Mattioli,G Feldmann,W Hendrickx,J Wint,J Jannin,J Slingenbergh (2004). Tsetse and trypanosomiasis intervention policies supporting sustainable animalagricultural development.
  13. Vincent Delespaux,Dirk Geysen,Peter Van Den Bossche,Stanny Geerts (2008). Molecular tools for the rapid detection of drug resistance in animal trypanosomes.
  14. K Sones (2001). NIH Partners with Pharmaceutical Companies to Promote Research on Osteoarthritis.
  15. V Delespaux,H De Koning (2007). Drugs and drug resistance in African trypanosomiasis.
  16. Who (2005). Guidelines for HIV post-exposure prophylaxis. Web annex C. PEP dosages.
  17. Richard Gleckman,Noel Blagg,Dennis Joubert (1981). Trimethoprim: Mechanisms of Action, Antimicrobial Activity, Bacterial Resistance, Pharmacokinetics, Adverse Reactions, and Therapeutic Indications.
  18. Gary Wormser,Gerald Keusch,Rennie Heel (1982). Co-trimoxazole (Trimethoprim-sulfamethoxazole) An Updated Review of its Antibacterial Activity and Clinical Efficacy.
  19. Gary Kalkut (1998). Sulfonamides and Trimethoprim.
  20. Y Hong,P Hossler,D Calhoun,S Meshnick (1995). Inhibition of recombinant Pneumocystis carinii dihydropteroate synthetase by sulfa drugs.
  21. K Pattishall,J Acar,J Burchall,F Goldstein,R Harvey (1977). Two distinct types of trimethoprim-resistant dihydrofolate reductase specified by R-plasmids of different compatibility groups..
  22. J Darrell,L Garrod,Pamela Waterworth (1968). Trimethoprim: laboratory and clinical studies.
  23. J Wilcke (1988). Therapeutic application of sulfadiazine/trimethoprim in dogs and cats: a review.
  24. E Böhni (1969). Chemotherapeutic activity of the combination of trimethoprim and sulfamethoxazole in infections of mice.
  25. Gary Wormser,Gerald Keusch,Rennie Heel (1982). Co-trimoxazole (Trimethoprim-sulfamethoxazole) An Updated Review of its Antibacterial Activity and Clinical Efficacy.
  26. Sam Kant,Avi Rosenberg,Fred Wigley (1999). Renal biopsy teaching case: A patient with scleroderma, hypertension, acute kidney injury and PR3 ANCA positivity.
  27. J Keystone,P Kozarsky (2000). Isospora belli, Sarcocystis species, Blastocystis hominis, and Cyclospora. Mandell, Douglas & Bennett's principles and practice of infectious diseases.
  28. K Sones (2001). NIH Partners with Pharmaceutical Companies to Promote Research on Osteoarthritis.
  29. (2012). Health hazard evaluation report: HETA-90-390-2065 and MHETA-86-012-2065, R. T. Vanderbilt Company, Gouverneur, New York..
  30. W Brent,H Gunderson Gigi,K Ross,C John (2001). What Do We Really Know about Antibiotics Pharmacodynamics?.
  31. L Suni,H Hiroaki,M Megumi,M Hidenori,K Aoko,C Ying,U Kozo,K Masayasu,N Yasumitsu,O Takemi (2014). Immunostimulation by Silica Particles and the Development of Autoimmune Dysregulation.
  32. S Lee,H Hayashi,M Maeda,H Matsuzaki,N Kumagai-Tkei (2014). Immunostimulation by Silica particles and the development of autoimmune dysregultion. Immune Response Activation.
  33. Madike Ezeibe,Anthony Egbuji,Obianuju Okoroafor,James Eze,Omadi Ijabo,Augustine Ngene,Ikechukwu Eze,Joeseph Ugonabo,Mary Sanda,Ijeoma Mbuko (2011). Antiviral Effects of a Synthetic Aluminium-Magnesium Silicate on Avian Influenza Virus.

Funding

No external funding was declared for this work.

Conflict of Interest

The authors declare no conflict of interest.

Ethical Approval

No ethics committee approval was required for this article type.

Data Availability

Not applicable for this article.

How to Cite This Article

M. C. O. Ezeibe. 2020. \u201cAntivirt ®{Al 4 (SiO 4 ) 3 + 3Mg 2 SiO 4 → 2Al 2 Mg 3 (SiO 4 ) 3 } Enhances Efficacy of Co-trimoxazole in Terminating Experimental Trypanosome Infections in Mice\u201d. Global Journal of Medical Research - G: Veterinary Science & Medicine GJMR-G Volume 20 (GJMR Volume 20 Issue G3): .

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Crossref Journal DOI 10.17406/gjmra

Print ISSN 0975-5888

e-ISSN 2249-4618

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GJMR-G Classification: NLMC Code: QW 70
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v1.2

Issue date

September 29, 2020

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en
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Both bacteria and protozoa require Folic acid for replication and Cotrimoxazole inhibits synthesis of the vitamin. For its mechanism of inhibiting Folic acid, the medicine has been in use as antibacterial drug for many decades but it is not being used to treat trypanosomosis (protozoan disease). To enhance anti-Folic acid activity of the medicine in order to improve its anti-trypanosome efficacy and make it function as new medicine for sleeping sickness (tropical disease of man and animals) it was stabilized with Antivirt® (Medicinal synthetic Aluminum-magnesium silicate). At 100 % of its antibacterial dose, Cotrimoxazole significantly reduced (P≤ 0.05) trypanosome parasitemia in mice, from 12.76±1.20 to 5. 87± 0.43. When it was stabilized with the Antivirt®, 75 % of the antibacterial dose had slight reduction (P≥ 0.05) in the trypanosome parasitemia (11.30±1.01) while the 100 % -dose achieved zero (0.00±00) trypanosome parasitemia and improved total WBC counts (immunity) from 1.50±0.16 to 2.86±0.38.

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Antivirt ®{Al 4 (SiO 4 ) 3 + 3Mg 2 SiO 4 → 2Al 2 Mg 3 (SiO 4 ) 3 } Enhances Efficacy of Co-trimoxazole in Terminating Experimental Trypanosome Infections in Mice

M. C. O. Ezeibe
M. C. O. Ezeibe Michael Okpara University of Agriculture
M. I. Ezeja
M. I. Ezeja
C. A
C. A
I.O. Onyeachonam
I.O. Onyeachonam
M. E. Sanda
M. E. Sanda
I. J. Ogbonna
I. J. Ogbonna
E. Kalu
E. Kalu
N.U. Njoku
N.U. Njoku
M.I. Udobi
M.I. Udobi

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