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2. Bromocriptine - Wikipedia

   en.wikipedia.org/wiki/Bromocriptine

   Bromocriptine, originally marketed as Parlodel and subsequently under many brand names, [1] is an ergoline derivative and dopamine agonist that is used in the treatment of pituitary tumors, Parkinson's disease, hyperprolactinaemia, neuroleptic malignant syndrome, and, as an adjunct, type 2 diabetes.

3. Cabergoline - Wikipedia

   en.wikipedia.org/wiki/Cabergoline

   Cabergoline is frequently used as a first-line agent in the management of prolactinomas due to its higher affinity for D 2 receptor sites, less severe side effects, and more convenient dosing schedule than the older bromocriptine, though in pregnancy bromocriptine is often still chosen since there is less data on safety in pregnancy for ...

4. Ergotamine - Wikipedia

   en.wikipedia.org/wiki/Ergotamine

   Ergotamine interacts with serotonin, adrenergic, and dopamine receptors. [17] [18] It is an agonist of serotonin receptors including the 5-HT 1 and 5-HT 2 subtypes. [17]Ergotamine is an agonist of the serotonin 5-HT 2B receptor and has been associated with cardiac valvulopathy. [19]

5. Bromopride - Wikipedia

   en.wikipedia.org/wiki/Bromopride

   Bromopride is indicated in the treatment of nausea and vomiting, including postoperative nausea and vomiting (PONV); gastroesophageal reflux disease (GERD/GORD); and as preparation for endoscopy and radiographic studies of the gastrointestinal tract.

6. Ketamine - Wikipedia

   en.wikipedia.org/wiki/Ketamine

   [107] [123] [124] However, later studies by different researchers found the affinity of ketamine of >10 μM for the regular human and rat D 2 receptors, [102] [108] [109] Moreover, whereas D 2 receptor agonists such as bromocriptine can rapidly and powerfully suppress prolactin secretion, [125] subanesthetic doses of ketamine have not been ...

7. Pergolide - Wikipedia

   en.wikipedia.org/wiki/Pergolide

   Pergolide is not currently available in the United States for human use. This problem is thought to be due to pergolide's action at the 5-HT 2B serotonin receptors of cardiac myocytes, causing proliferative valve disease by the same mechanism as ergotamine , methysergide , fenfluramine , and other serotonin 5-HT 2B agonists, including serotonin ...

8. Dying To Be Free - The Huffington Post

   projects.huffingtonpost.com/dying-to-be-free...

   Like methadone, Suboxone blocks both the effects of heroin withdrawal and an addict’s craving and, if used properly, does it without causing intoxication. Unlike methadone, it can be prescribed by a certified family physician and taken at home, meaning a recovering addict can lead a normal life, without a daily early-morning commute to a clinic.

9. Bornaprine - Wikipedia

   en.wikipedia.org/wiki/Bornaprine

   Bornaprine Pathway. Bornaprine is an antimuscarinic agent that nonselectively antagonizes muscarinic acetylcholine receptors, M1 and M2. [8] Bornaprine has been characterized as a very potent anticholinergic medication and further clinical trials have indicated its effectiveness at treating parkinsonian tremors.