L-cycloserine

From WikiMD's Wellness Encyclopedia

L-Cycloserine, also known as D-cycloserine and by its chemical name 4-amino-3-isoxazolidinone, is an antibiotic used to treat tuberculosis. This medication is particularly employed in cases where the disease has become resistant to conventional treatments. Beyond its primary use in combating tuberculosis, L-cycloserine has found a secondary application in the field of neuroscience, where it is used as a cognitive enhancer due to its action as a partial agonist at the NMDA receptor.

Medical Uses[edit | edit source]

L-Cycloserine is primarily used in combination with other antibiotics to treat multidrug-resistant tuberculosis (MDR-TB). Its effectiveness is most pronounced when the disease has shown resistance to first-line treatment options. The drug is administered orally, and its dosage is determined by the healthcare provider based on the severity of the condition and the patient's response to treatment.

Mechanism of Action[edit | edit source]

The antibiotic properties of L-cycloserine derive from its ability to inhibit cell wall synthesis in bacteria. It specifically targets the enzyme alanine racemase and D-alanine:D-alanine ligase, which are crucial for the production of peptidoglycan, a major component of the bacterial cell wall. By inhibiting these enzymes, L-cycloserine effectively hampers the growth and reproduction of bacteria.

In neuroscience, L-cycloserine's role as a partial agonist at the NMDA receptor is of significant interest. The NMDA receptor is involved in synaptic plasticity and memory formation. By modulating this receptor, L-cycloserine has the potential to enhance cognitive functions, making it a subject of research for the treatment of psychiatric disorders such as schizophrenia and depression, as well as for enhancing cognitive recovery in neurological conditions like stroke and traumatic brain injury.

Side Effects[edit | edit source]

The use of L-cycloserine can be associated with several side effects, ranging from mild to severe. Common adverse effects include headache, dizziness, and somnolence. More serious side effects may include psychiatric symptoms such as anxiety, depression, and even suicidal thoughts. Due to its impact on the central nervous system, careful monitoring by healthcare providers is recommended during treatment with L-cycloserine.

Pharmacokinetics[edit | edit source]

L-cycloserine is well absorbed from the gastrointestinal tract, with peak plasma concentrations occurring within a few hours after oral administration. The drug is metabolized minimally and is primarily excreted unchanged in the urine. Its half-life allows for dosing once or twice daily, depending on the specific needs of the treatment regimen.

History[edit | edit source]

L-cycloserine was discovered in the early 1950s as a product of the bacterium Streptomyces orchidaceus. It was initially developed as an antibiotic for the treatment of tuberculosis. Over the years, its use has been limited due to the development of resistance and the availability of more effective treatments. However, its unique action on the central nervous system has led to renewed interest in its potential applications in psychiatry and neurology.

Conclusion[edit | edit source]

L-cycloserine is a versatile drug with applications in both the treatment of multidrug-resistant tuberculosis and the potential enhancement of cognitive functions. Its dual action as an antibiotic and a partial NMDA receptor agonist makes it a unique subject of ongoing research. Despite its benefits, the drug's side effects necessitate careful monitoring during treatment.


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Contributors: Prab R. Tumpati, MD