λ©ν ν΄λ‘νλΌλ§μ΄λ
λ©ν ν΄λ‘νλΌλ§μ΄λλ μμνμμ λ리 μ¬μ©λλ **μμ₯κ΄ μ΄λ μ΄μ§μ ** λ° **νꡬν μ **μ λλ€. * **μ΄λ μ΄μ§ ν¨κ³Ό**: μ£Όλ‘ μλΆ μμ₯κ΄(μ λ° μμ₯)μ μμ©νλ©° κ²°μ₯μλ κ±°μ μν₯μ λ―ΈμΉμ§ μμ΅λλ€. μ μ 체, μμλ μλ₯ λ° μμ ν μ₯νμμ¦μ μμμ μΌλ‘ μ¬μ©λ©λλ€. * **νꡬν ν¨κ³Ό**: κ°λ ννμμ©μ²΄ μ λ°λ(CRTZ)μ λνλ―Ό μμ©μ²΄κ° νλΆνμ¬ λ§€μ° ν¨κ³Όμ μ λλ€. λ°λ©΄ κ³ μμ΄λ D2 μμ©μ²΄κ° μ μ΄ νꡬν μ λ‘μμ μ λ’°μ±μ΄ λ¨μ΄μ§λλ€(λ§λ‘νΌννΈμ κ°μ NK-1 κΈΈνμ κ° μ’ μ’ μ νΈλ¨). **μμ μμ **: * ν보λ°μ΄λ¬μ€ μ₯μΌμ΄λ κΈμ± μ·μ₯μΌκ³Ό κ°μ μ¬κ°ν μνμ λν΄ μ§μμ μ λ§₯ μ£Όμ (CRI)μΌλ‘ μμ£Ό ν¬μ¬λ©λλ€. * νμ‘λμ₯λ²½μ ν΅κ³ΌνκΈ° λλ¬Έμ, νΉν κ³ μ©λμ΄λ λ§κ³Ό κ°μ΄ λ―Όκ°ν μ’ μμ λμ λλ μΆμ²΄μΈλ‘ λΆμμ©(μ: λ¨λ¦Ό, μμ λΆμ λͺ»ν¨, κ΄λ νλ)μ μ λ°ν μ μμ΅λλ€.
μμ© κΈ°μ : Metoclopramide exerts its effects through both peripheral gastrointestinal and central nervous system mechanisms: * **Peripheral (GI Tract)**: Sensitizes upper GI smooth muscle to **acetylcholine** β increases tone and amplitude of gastric contractions, relaxes the pyloric sphincter, and increases duodenal and jejunal peristalsis. It also increases lower esophageal sphincter (LES) pressure, reducing reflux. * **Central (CNS)**: Antagonizes **Dopamine (D2)** receptors in the **Chemoreceptor Trigger Zone (CRTZ)** β blocks emetic signaling to the vomiting center, providing a potent central antiemetic effect. * **Additional Mechanisms**: At higher doses, it exhibits weak **5-HT3 (Serotonin)** receptor antagonism and **5-HT4** receptor agonism, further contributing to its antiemetic and prokinetic profiles.
λλ¬Ό μ’ λ³ μ©λ
- As a prokinetic for adjunctive treatment of esophagitis Β· 0.2-0.4 mg/kg PO q8h Β· PO Β· q8h Β· Cisapride considered superior.
- General use Β· 0.2-0.4 mg/kg PO, SC 3-4 times daily; or as a continuous IV infusion (1-2 mg/kg per day) Β· PO/SC/IV Β· tid-qid or CRI
- General use Β· 0.2-0.5 mg/kg q8h PO or parenterally (may be given as a constant rate IV infusion at 0.01-0.02 mg/kg/hr) Β· PO/IV/IM/SC Β· q8h or CRI
- To increase bladder contractility Β· 0.2-0.5 mg/kg PO q8h Β· PO Β· q8h
- To induce milk let-down for secondary agalactia Β· 0.1-0.2 mg/kg SC q12h Β· SC Β· q12h Β· Used to promote milk production.
- To stimulate the gastrointestinal tract Β· 0.04 mg/kg/hr as a CRI Β· IV Β· CRI Β· ARCI UCGFS Class 4 Drug.
- For reflux esophagitis Β· 0.02-0.1 mg/kg SC q4-12 hours Β· SC Β· q4-12h Β· Horses may be prone to extrapyramidal neurologic side effects.
- General therapeutics (Rabbits) Β· 0.2-1 mg/kg PO or SC q6-8h Β· PO/SC Β· q6-8h
- To assist in removing gastric hairballs (Rabbits) Β· 0.5 mg/kg PO once a day (up to three times a day) Β· PO Β· sid to tid
ν¬μ¬ κ²½λ‘
κΈκΈ°
- GI hemorrhage
- GI obstruction or perforation
- Hypersensitivity to metoclopramide
- Seizure disorders (relatively contraindicated, lowers seizure threshold)
- Head trauma
- Pheochromocytoma (may induce hypertensive crisis)
- Concurrent phenothiazine therapy
- Dogs with pseudopregnancy (stimulates prolactin release)
- Gastrointestinal obstruction
- Gastrointestinal perforation
- Gastrointestinal hemorrhage
- Seizure disorders (epilepsy)
- Pheochromocytoma
μ΄μλ°μ
- Dogs: Changes in mentation and behavior (motor restlessness, involuntary spasms, aggression, hyperactivity to drowsiness/depression), constipation
- Cats: Frenzied behavior, disorientation, constipation
- Horses: Severe CNS effects (IV use), alternating sedation and excitement, behavioral changes, abdominal pain
- Extrapyramidal effects (tremors, rigid posture)
- Nausea and diarrhea
- Transient hypertension
- Elevated prolactin levels
- Extrapyramidal signs (tremors, twitching, hyperactivity, restlessness)
- Sedation
- Constipation or diarrhea
- Changes in mentation or behavior
μ½λ¬Ό μνΈμμ©
- Aspirin, Acetaminophen, Alcohol Β· Metoclopramide may enhance the absorption of these agents.
- Anesthetics Β· Acute hypotension has been reported if metoclopramide is used concurrently IV.
- Atropine (and anticholinergics) Β· May antagonize the GI motility effects of metoclopramide.
- Cephalexin Β· Oral metoclopramide increases cephalexin peak plasma concentrations and AUC in dogs.
- Cholinergic Drugs (e.g., bethanechol) Β· May enhance metoclopramide's GI effects.
- CNS Depressants Β· Metoclopramide may enhance CNS depressant effects. Β· moderate
- Cyclosporine Β· Metoclopramide increases the rate and extent of GI absorption.
- Opiate Analgesics Β· May antagonize the GI motility effects and enhance metoclopramide's CNS effects.
- MAO Inhibitors (e.g., amitraz, selegiline) Β· Could cause hypertension.
- Phenothiazines and Butyrophenones Β· May potentiate the extrapyramidal effects of metoclopramide.
- Propofol Β· Reduces induction requirements of propofol by 20-25%.
- SSRI Antidepressants Β· Potential for enhanced extrapyramidal effects.
- Tetracyclines Β· Metoclopramide increases the rate and extent of GI absorption.
λͺ¨λν°λ§
- Clinical efficacy (resolution of vomiting, improved GI transit)
- Adverse effects (especially CNS and extrapyramidal signs)
- Clinical response (reduction in vomiting, improved gastric emptying)
- Hydration status and electrolyte balance
- Signs of extrapyramidal adverse effects (twitching, restlessness)
κ³Όμ©λ
The oral LD50 doses are very high (465-870 mg/kg in laboratory animals), making death from oral overdose unlikely in veterinary patients. **Clinical Signs of Toxicity**: * Sedation, ataxia, agitation * Extrapyramidal effects (tremors, rigidity, spasms) * Nausea, vomiting, constipation **Treatment**: * No specific antidote exists. * If ingestion was recent, empty the stomach using standard protocols. * **Anticholinergic agents** that enter the CNS (e.g., **diphenhydramine** at 2.2 mg/kg IV, or benztropine) are highly effective in controlling extrapyramidal effects. * Peritoneal dialysis or hemodialysis is not effective for drug removal.
VetSheet μ½λ¬Ό λ νΌλ°μ€λ λ©΄ν μμ μ λ¬Έκ°λ₯Ό μν μμ μμ¬κ²°μ 보쑰 λꡬμ΄λ©°, μ λ¬Έμ νλ¨μ΄λ μ μ‘°μ¬μ μ΅μ λΌλ²¨μ λμ νμ§ μμ΅λλ€.