Oral pain relievers, also known as analgesics, work by interfering with the body's pain signaling pathways. They can be broadly categorized into non-opioid analgesics, opioid analgesics, and adjuvant analgesics.
1. **Non-opioid analgesics**: This category includes drugs like acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and aspirin. NSAIDs work by inhibiting the cyclooxygenase (COX) enzymes, COX-1 and COX-2, which are involved in the production of prostaglandins. Prostaglandins are chemicals that promote inflammation, pain, and fever. By reducing their production, NSAIDs alleviate pain and inflammation. Acetaminophen, on the other hand, is believed to work centrally in the brain to reduce pain and fever, though its exact mechanism is not fully understood.
2. **Opioid analgesics**: These include drugs like morphine, oxycodone, and codeine. Opioids work by binding to specific receptors in the brain, spinal cord, and other parts of the body known as opioid receptors. This binding blocks the transmission of pain signals and alters the perception of pain, providing relief. Opioids can also produce feelings of euphoria, which is why they have a high potential for addiction and abuse.
3. **Adjuvant analgesics**: These are drugs that are not primarily designed to control pain but can be effective for certain types of pain. Examples include certain antidepressants and anticonvulsants. They work by modulating neurotransmitter levels or stabilizing nerve cell membranes, thereby reducing pain signaling.
Overall, oral pain relievers target different aspects of the pain pathway, either by reducing the production of pain-inducing chemicals, blocking pain signal transmission, or altering pain perception, to provide relief.