Subject(s)
Pain Management/history , Pain/history , Anesthesia/history , Anesthesia/methods , Animals , Aspirin/history , Brain/pathology , Brain/physiopathology , Cocaine/administration & dosage , Cocaine/history , Cocaine/therapeutic use , Complex Regional Pain Syndromes/history , Dental Caries/history , Dental Caries/therapy , Electric Stimulation Therapy/history , Endorphins/history , Endorphins/metabolism , Female , History, 17th Century , History, 18th Century , History, 19th Century , History, 20th Century , History, 21st Century , History, Ancient , Humans , Hyoscyamus , Isoquinolines/history , Isoquinolines/metabolism , Male , Mice , Microglia/physiology , Models, Psychological , Morphine/history , Morphine/pharmacology , Morphine/therapeutic use , Nerve Block/history , Neuroimaging/history , Nitrous Oxide/administration & dosage , Nitrous Oxide/history , Nitrous Oxide/pharmacology , Nociceptors/metabolism , Opium/history , Pain/physiopathology , Receptors, Dopamine/metabolism , Sex Characteristics , Spinal Puncture , T-Lymphocytes/physiologyABSTRACT
IMPORTANCE OF THE FIELD: Since the advent of the 5-hydroxytryptamine 3 receptor antagonists (5-HT3RAs) in the 1990s, dramatic improvements have been achieved in the field of antiemetic therapy. The enhanced prevention of delayed and overall chemotherapy-induced nausea and vomiting (CINV) offered by palonosetron, a second-generation 5-HT3RA and aprepitant, the first neurokinin-1 receptor antagonists (NK-1RA) represent the only significant treatment advances in the past decade. While initial trials of single-dose palonosetron indicated a potential benefit over first-generation 5-HT3RAs, only recently have new data become available, increasing the weight of evidence distinguishing it as a new 5-HT3RA in the class. AREAS COVERED IN THIS REVIEW: History of antiemetics and palonosetron, including clinical trials and pharmacological research, and literature published between 1981 and 2010 are covered. WHAT THE READER WILL GAIN: Unique pharmacological characteristics of palonosetron exhibiting prolonged half-life, high receptor affinity, allosteric interactions and positive cooperativity with 5-HT3 receptor resulting in long-term alteration and internalization of this receptor may explain the clinical observation of palonosetron. TAKE HOME MESSAGE: This review of recent progress in antiemetic therapy focuses on the newest data on palonosetron and discusses future trials and implications for clinical practice, with the overall goal of learning from history.
Subject(s)
Antiemetics/therapeutic use , Antineoplastic Agents/adverse effects , Dopamine Antagonists/therapeutic use , Isoquinolines/therapeutic use , Nausea/prevention & control , Quinuclidines/therapeutic use , Serotonin 5-HT3 Receptor Antagonists , Vomiting/prevention & control , Animals , Antiemetics/adverse effects , Antiemetics/history , Antiemetics/pharmacokinetics , Dopamine Antagonists/adverse effects , Dopamine Antagonists/history , Dopamine Antagonists/pharmacokinetics , Evidence-Based Medicine , History, 20th Century , History, 21st Century , Humans , Isoquinolines/adverse effects , Isoquinolines/history , Isoquinolines/pharmacokinetics , Nausea/chemically induced , Palonosetron , Quinuclidines/adverse effects , Quinuclidines/history , Quinuclidines/pharmacokinetics , Treatment Outcome , Vomiting/chemically inducedABSTRACT
The role of histamine in hypersensitivity reactions justifies the use of antagonistic medication. The symptomatic action of the antihistamines has led many workers to forget the role of the drug in reducing histamine (hypohistaminic), in which interest should remain as a curative and mainly preventive medication. The main indications for the action of this drug at the level of physiopathological mechanism involved are: disorders that implicate the production of endogenous histamine, prevention of histamine release, reduction of over-production of histamine by regulation of receptor saturation, symptomatic action without side effects.