Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Methylating agents as trypanocides.

P G Penketh1, K Shyam, A A Divo

  • 1Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510.

Journal of Medicinal Chemistry
|February 1, 1990
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A simple and inexpensive method to control oxygen concentrations within physiological and neoplastic ranges.

Analytical biochemistry·2015
Same author

1,2-Bis(methylsulfonyl)-1-(2-chloroethyl)-2-[(methylamino)carbonyl]hydrazine (VNP40101M): I. Direct inhibition of O6-alkylguanine-DNA alkyltransferase (AGT) by electrophilic species generated by decomposition.

Cancer chemotherapy and pharmacology·2004
Same author

1,2-Bis(methylsulfonyl)-1-(2-chloroethyl)-2-[(methylamino)carbonyl]hydrazine (VNP40101M): II. Role of O6-alkylguanine-DNA alkyltransferase in cytotoxicity.

Cancer chemotherapy and pharmacology·2003
Same author

Synthesis of halogen-substituted 3-deazaadenosine and 3-deazaguanosine analogues as potential antitumor/antiviral agents.

Nucleosides, nucleotides & nucleic acids·2002
Same author

Reversal of mitomycin C resistance by overexpression of bioreductive enzymes in Chinese hamster ovary cells.

Cancer research·2001
Same author

Inhibition of 20 S and 26 S proteasome activity by lithium chloride: impact on the differentiation of leukemia cells by all-trans retinoic acid.

The Journal of biological chemistry·2001

Methylating agents effectively treat African trypanosomiasis in mice by halting parasite proliferation and inducing differentiation. These compounds offer new biochemical tools for studying trypanosome development.

Area of Science:

  • Pharmacology
  • Parasitology
  • Biochemistry

Background:

  • African trypanosomiasis is a significant parasitic disease.
  • Novel therapeutic strategies are needed to combat the disease.

Purpose of the Study:

  • To evaluate the therapeutic activity of methylating agents against African trypanosomiasis.
  • To investigate the effects of methylating agents on trypanosome morphology and differentiation.

Main Methods:

  • Administration of various methylating agents to murine models of African trypanosomiasis.
  • Observation of trypanosome proliferation, morphology, and differentiation patterns.
  • Biochemical analysis of trypanosome populations.

Main Results:

Related Experiment Videos

  • Methylating agents demonstrated therapeutic activity against murine African trypanosomiasis.
  • High doses halted trypanosome proliferation and induced abnormal cell forms.
  • Low doses induced synchronous differentiation into short-stumpy forms.
  • Conclusions:

    • Methylating agents show promise as treatments for African trypanosomiasis.
    • These agents can be utilized as biochemical tools to study trypanosome differentiation.