Tespral Od
Tespral Od Uses, Dosage, Side Effects, Food Interaction and all others data.
Tespral Od is a dopamine D2 antagonist with acetylcholinesterase inhibitory actions.
Trade Name | Tespral Od |
Generic | Itopride |
Itopride Other Names | Itopride |
Weight | 150mg |
Type | Capsule |
Formula | C20H26N2O4 |
Weight | Average: 358.4314 Monoisotopic: 358.18925733 |
Groups | Investigational |
Therapeutic Class | |
Manufacturer | Martin Dow Pharmaceuticals (pak) Ltd, |
Available Country | Pakistan |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Tespral Od is an acetylcholine esterase inhibitor and dopamine D2 receptor antagonist used to treat symptoms of functional dyspepsia such as nausea and vomiting.
Investigated for use/treatment in gastrointestinal diseases and disorders (miscellaneous).
Tespral Od is also used to associated treatment for these conditions: Abdominal Pain, Dyspepsia, Functional Dyspepsia, Gastroenteritis, Loss of Appetite, Nausea, Nausea and vomiting, Vomiting, Abdominal bloating, Pyrosis, Stomach discomfort
How Tespral Od works
Tespral Od has anticholinesterase (AchE) activity as well as dopamine D2 receptor antagonistic activity. It is well established that M3 receptors exist on the smooth muscle layer throughout the gut and acetylcholine (ACh) released from enteric nerve endings stimulates the contraction of smooth muscle through M3 receptors. The enzyme AChE hydrolyses the released ACh, inactivates it and thus inhibits the gastric motility leading to various digestive disorders. Besides ACh, dopamine is present in significant amounts in the gastrointestinal tract and has several inhibitory effects on gastrointestinal motility, including reduction of lower esophageal sphincter and intragastric pressure. These effects appear to result from suppression of ACh release from the myenteric motor neurons and are mediated by the D2 subtype of dopamine receptors. Tespral Od, by virtue of its dopamine D2 receptor antagonism, removes the inhibitory effects on Ach release. It also inhibits the enzyme AchE which prevents the degradation of ACh. The net effect is an increase in ACh concentration, which in turn, promotes gastric motility, increases the lower esophageal sphincter pressure, accelerates gastric emptying and improves gastro-duodenal coordination. This dual mode of action of Tespral Od is unique and different from the actions of other prokinetic agents available in the market.
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