[L. inhibere, to hold back, restrain]
An agent that blocks a cellular receptor, stops a chemical reaction, prevents an enzyme from working, or suppresses a muscle or nerve.
SEE: Alpha-2 antiplasmin.
An oral drug that lowers blood sugars by preventing carbohydrate absorption from the gastrointestinal tract.
A medication to treat benign prostatic hyperplasia. It blocks the conversion of testosterone to dihydrotestosterone.
ABBR: ACE inhibitor Any of the therapeutic agents that inhibit conversion of angiotensin I to angiotensin II. ACE inhibitors are used to treat hypertension and heart failure and to protect kidney function in patients with diabetes mellitus.
Any of a class of drugs that block the synthesis of estrogen in the body. A number of these agents have been developed to treat breast cancer, which is often a hormone-responsive malignancy.
SEE: Entry inhibitor.
Any of a class of drugs that prevent or retard osteoporosis. Examples include the bisphosphonates.
Patients with achalasia should avoid these medications because bisphosphonates may cause inflammation and ulceration in the esophagus.
ABBR: COMT inhibitor An inhibitor such as entacapone or tolcapone used to treat the “wearing off” phenomenon of Parkinson disease. “Wearing off” is the reduction of the rate at which levodopa is metabolized. The COMT inhibitors reduce this rate and prolong the effectiveness of levadopa.
Any agent that prevents chitin, a critical component of fungal cell walls, from forming. Agents from this class may be used to treat serious fungal infections, such as coccidiomycosis.
Any drug that inhibits the transfer of cholesteryl esters from high-density lipoproteins (HDLs) to other lipoproteins. Drugs from this class increase HDL levels, potentially improving the lipid profiles of patients and decreasing their risk of atherosclerosis.
ABBR: ChEI Any of a class of drugs that prevent the degradation of the neurotransmitter acetylcholine, which is involved in memory and learning. Drugs from this class are used to treat Alzheimer dementia.
SYN: SEE: acetylcholinesterase inhibitor
1. A chemical that binds to or blocks another reagent from participating in a reaction.
2. A medication, hormone, or other intercellular messenger that binds and blocks the cellular receptor or target enzyme of another agent. Drugs that act by competitive inhibition may treat or prevent disease by inactivating pathogenic enzymes or by blocking the effects of hormones or precursor molecules. For example, protease inhibitors interfere with production of HIV by binding and inactivating the protease enzyme; selective estrogen-receptor modulators limit the impact of estrogen by replacing this hormone on cells sensitive to its effects.
Any agent that suppresses inflammation by blocking the inflammatory effects of cyclooxygenase.
ABBR: DPP-4 inhibitor SEE: Gliptin.
ABBR: DTI Any medication or substance that interferes with the coagulation of blood by blocking the action of thrombin. Unlike heparins, which are anticoagulants that require the presence of antithrombin to inactivate thrombin, DTIs exert their effects without an intermediary. DTIs can be used to treat and prevent clots in both arteries and veins (heparin and warfarin are usually preferred for these uses). They are an alternative to heparin in patients with a history of heparin-induced thrombocytopenia. The primary side effect of DTIs is bleeding.
An antidepressant medication that works by blocking the reuptake of both serotonin and norepinephrine.
Any agent that prevents a pathogen, e.g., HIV, from binding to cell membranes and infecting cells.
SYN: SEE: attachment
Any drug that prevents blood coagulation by interfering with the activity of coagulation Factor Xa. Examples include: apixaban, edoxaban, and rivaroxaban.
Any drug that prevents a virus from attaching itself to the membrane of a vulnerable cell.
Any of a class of drugs that block the fibrinogen receptor on the surface of platelets. Drugs from this class are used to treat acute myocardial infarction, unstable angina pectoris, and other acute coronary syndromes. The most common side effect of treatment with these drugs is bleeding.
Any drug that blocks the replication of herpes simplex virus by targeting enzymes crucial to viral DNA synthesis.
ABBR: INSTI Any agent that prevents HIV from inserting its viral DNA into host cell chromosomes.
Any antiretroviral drug that blocks the effect of integrase.
An agent that inhibits cancer cells by blocking their abilities to invade tissues, demand new blood supply, and metastasize.
Any of numerous compounds that inhibit the activity of the metalloproteinase family of enzymes. These agents share the ability to suppress or eliminate the enzyme activity of the metalloproteinases. Agents identified in this group include the tetracycline antibiotics, numerous specially designed synthetic peptides and proteins, chemicals such as ethylenediaminetetra-acetic acid (EDTA), and a variety of agents used in cancer chemotherapy.
SYN: SEE: metalloprotease inhibitor
ABBR: MAOI Any of a group of drugs that can be used to treat depression and Parkinson disease. Nonselective versions of these medications produced hypertensive crises and other severe side effects when they were taken with tyramine-containing foods (some cheeses) and several other drugs. Newer members of this class of drugs do not have these effects, but should be used with caution, esp. by those taking selective serotonin reuptake inhibitors.
MAOIs may have unfavorable drug-drug interactions with many anesthetics and should be discontinued approximately 2 weeks before surgery.
Any of a class of antiviral drugs that block neuraminidase, which helps the influenza virus to bud from cells it has infected so that it can spread to other ciliated epithelial cells of the respiratory tract. Agents in this class include oseltamivir and zanamivir.
ABBR: NNRTI Any of a class of antiretroviral drugs used to treat those infected with HIV. NNRTIs bind with and inhibit the activity of reverse transcriptase, an enzyme needed to transcribe viral RNA into the host cell DNA. Examples include nevirapine, delavirdine, and efavirenz.
ABBR: NRTI Any of a class of antiretroviral drugs used to treat patients with HIV infection. NRTIs prevent transcription of viral RNA to host DNA by interfering with the action of the enzyme reverse transcriptase. Zidovudine, dideoxyinosine, zalcitabine, d4T, and abacavir are NRTIs.
SEE: reverse transcriptase inhibitor
Any of a class of drugs that bind to cellular receptors for low-density lipoproteins (LDLs). They are used to improve serum cholesterol levels by improving the clearance of LDLs from the circulation.
ABBR: PDE inhibitor Any agent that blocks phosphodiesterase, inhibiting the production of second messengers within cells, such as cyclic adenosine monophosphate or cyclic glucose monophosphate. Drugs that inhibit PDE include sildenafil and other agents used as positive inotropes and vasodilators in heart failure.
A monoclonal antibody used to treat elevated low density lipoprotein cholesterol levels.
A substance that inhibits the production of prostaglandins. Nonsteroidal and steroidal anti-inflammatory agents are two major categories of such inhibitors.
1. A substance that inhibits the action of enzymes.
2. Any of a class of medications that prevent immature virions (as of hepatitis viruses or HIV) from assembling into structures capable of replication.
ABBR: PPI Any of a class of medications that eliminate acid production in the stomach. These drugs are used to treat peptic ulcers, gastroesophageal reflux disease, infection with Heliobacter pylori, and related disorders. Omeprazole and lansoprazole are members of this drug class.
ABBR: RTI Any of a class of antiretroviral agents that competitively inhibit the reverse transcriptase enzyme of HIV and other viruses.
ABBR: SSRI Any of a class of drugs that interfere with serotonin transport and are used to treat depression, obsessive-compulsive behaviors, eating disorders, and social phobias. Examples include fluoxetine (Prozac), paroxetine (Paxil), and sertraline.
The use of SSRIs in the treatment of depression may sometimes be associated with an increased risk of suicide, esp. during the initiation of treatment. The risk is greatest among children and adolescents. All patients who begin treatment with SSRIs should be monitored closely for evidence that they intend to harm themselves.
ABBR: serpin Any of the compounds that inhibit platelet function and coagulation. Serpins have been used to reduce deposition of microemboli in cases of disseminated intravascular coagulation associated with sepsis.
ABBR: SNRI An antidepressant medication (such as duloxetine or venlafaxine) that elevates mood by blocking neurons from taking up both norepinephrine and serotonin. Combined reuptake inhibitors differ from medications such as sertraline (Zoloft) or fluoxetine (Prozac), which are relatively selective serotonin reuptake inhibitors, and from tricyclic antidepressants, which primarily prevent the reuptake of norepinephrine by brain cells. SNRIs treat neuropathic pain as well as depression.
Any drug, such as dapaglifozin or canagliflozin, that reduces serum blood sugars by increasing the urinary excretion of glucose.
Any drug that blocks the polymerization of microtubules in cells, and thereby preventing mitosis from occurring. An example of a drug from this class is colchicine.
A drug that blocks the effects of tumor necrosis factor alpha (TNF-α), a biologically active cytokine that is a critical element of the inflammatory response. Such drugs, which include adalimumab, etanercept, and infliximab, are agents used to treat autoimmune illnesses such as rheumatoid arthritis.
Because these drugs are immunologically active, patients with active infection or those with chronic infections such as tuberculosis should not use them. These agents also sometimes increase the risk of cancers and have rarely been associated with demyelinating diseases of the central nervous system such as multiple sclerosis.
Any of a class of medications that blocks the actions of both angiotensin-converting enzymes (ACE) and neural endopeptidase. Drugs from this class may be used to treat heart failure.
Any drug, such as allopurinol or febuxostat, that decreases serum uric acid concentrations by inhibiting the enzyme xanthine oxidase.
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