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Main Index>> Bacterial Cheomotherapy

Sulphonamides Chemotherapy
Antibiotics
Range of Antibiotic Actions
Classification of Antobiotics
Structure of Antibiotics
Phosphonomycin
Oxamycin (cycloserine)
Vancomycin and Ristocetin
Penicillins and Cephalosporins
Mechanism of Antibacterial Action
Antibiotics Affecting the Cell Wall Peptidoglycan Biosynthesis
Drugs Affecting the Cell Membrane
Phenols
Cationic Antispetics
Inhibiting DNA Synthesis
Inhibitors of Nucleotide Precursors Biosynthesis Azaserine and 6-diazo-5-oxo-L-norleucine (DON)
Hadacidin
Psicofuranine
Inhibitors of Polymerization
Actinomycin D
Acridines and Phenanthridines
Mitomycin and Porfiromycin
Rifamycins
Inhibitors of Protein Synthesis
Plasmids and Drug Resistance
Biochemical Mechanisms of Resistance
Alteration of Target Site
Blocking of Antibiotic Transport
Inactivation of Antibiotics OR Enzymatic Detoxification
Bypass Mechanisms
Inhibition of Protein Synthesis
 

Bacterial Cheomotherapy


Bacterial Cheomotherapy - Antimicrobial agents have been used in folk remedies from early times. The indians of Peru used cinchona, bark for treating malaria. The active principle of cinchona bark, quinine, was isolated in 1920. The ipecacuanha root was used in Brazil and Asia for treating amoebic dysentery. Its active constituent. emetin, was isolated in 1817, and    was shown to have a specific action against amoebic dysentery in 1891. The work of Pasteur and Koch established that microorganisms were the cause of infectious disease, Paul Ehrlich was the first to propose that infectious diseases might be curab1e by using chemicals that inhibit or kin the infectious agents, but do not harm the host at the concentration employed.

His studies with the vital dye methylene  blue showed that this slain concentrated in nervous tissue, and was readily taken up by malarial parasites in the blood. This specificity of staining led to the search for compounds with selective action against' microbial cells After testing hundreds of dyes he found (in 1904) Trypan red as effective against trypanosomiasis in horses. Later Koch found that arsenical atoxl cured sleeping sickness in humans. In 1910 Ehrlich discovered the famous organoarsenical compound salvarsan. 

which was active against the causative organisms of syphilis. It was he who first used the term Chemotherapy, According to his theory of drug action, cells possess chemical receptors to which the drugs bind. He recognized the importance of quantitative measurements to determine the drug dose that would be effective against the causative agent and not have toxic effects on the host He also pioneered method for screening a large number of compounds for biological activity in relation to chemical structure.

Chemical variants of effective compounds were then synthesized and tested to see whether they had improved antimicrobial activity and reduced toxicity. It was Ehrlich who thus established the principles of modern chemotherapy. Compounds that inhibit the proliferation of infective organisms are called chemotherapeutic agents. When there is reversible inhibition of, growth the compounds are said to be bacteriostatic.

Bacteriostats do not kill bacteria, but only prevent their multiplication. Bacteriostatic action usually offers sufficient protection, because the relatively small number of bacteria can be removed by the antibody and phagocytic defences of the body. Compounds with irreversibe lethal action are said to be bactericidal. 

 

Stages of Translation in Protein Synthesis
Initiation Process in Translation in Protein Synthesis
Elongation Process in Translation in Protein Synthesis
Termination Process in Translation in Protein Synthesis
Supernatant
Folic Acid Antagonists
Aminoalkyl Adenylates
Diptheria Toxin
30S/40S Ribosomal Subunits
Aminoglycosides
Streptomycin
Neomycin,Kanamycin and Gentamycin
Tetracyclines
Edeine
50S/60S Ribosomal Subunit
Chloramphenicol
Macrolides
Lincosamides
Puromycin
Sparsomycin
Glutarimides
Cycloheximide
Ipeal Alkaloids
Emetine