ํ๋ฅด๊ณจ๋ฆฌ๋
ํ๋ฅด๊ณจ๋ฆฌ๋๋ ๋งฅ๊ฐ ์ ๋์ฒด ๋ํ๋ฏผ ์์ฉ์ ๋ก, ์์ํ์์๋ ์ฃผ๋ก ๋ง์ **๋ํ์์ฒด ์ค์ฝ ๊ธฐ๋ฅ ์ฅ์ (PPID, ์ผ๋ช ๋ง ์ฟ ์ฑ ์ฆํ๊ตฐ)** ์น๋ฃ๋ฅผ ์ํ **ํ์ค ์น๋ฃ์ (Gold standard)**๋ก ์ฌ์ฉ๋ฉ๋๋ค. * **์์์ ์ค์์ฑ**: ๋ค๋ชจ์ฆ(ํธ๊ฐ์ด ์ง์ฐ/๊ธด ํธ), ๋ฌด๊ธฐ๋ ฅ, ๊ทผ์ก ์์ถ, ์ ์ฝ์ผ ๋ฑ ๋ง์ PPID ์์ ์ฆ์์ ๊ด๋ฆฌํ๋ ๋ฐ ๊ฐ์ฅ ํจ๊ณผ์ ์ธ ์ฝ๋ฌผ ์๋ฒ์ ๋๋ค. * **๊ตฌ์ ๋ฐฉ๋ฒ**: ์ธ์ฒด์ฉ ์ฝ๋ฌผ์ ์ฌ์ฅ ํ๋ง ์งํ ์ํ์ผ๋ก ์ธํด 2007๋ ๋ฏธ๊ตญ ์์ฅ์์ ์ฒ ์๋์์ผ๋ฏ๋ก, ํ์ฌ ์์ํ์ฉ์ผ๋ก๋ ์กฐ์ ์ฝ๊ตญ(compounding pharmacy)์ ํตํด์๋ง ๋ ์ ์ ์ผ๋ก ๊ตฌํ ์ ์์ต๋๋ค. * **๋ด์ฝ์ฑ**: ๋ง์๊ฒ ์ผ๋ฐ์ ์ผ๋ก ๋งค์ฐ ๋ด์ฝ์ฑ์ด ์ข์ผ๋, ์น๋ฃ ์ด๊ธฐ์๋ ์ผ์์ ์ธ ์์ ๋ถ์ง์ด ๋ฐ์ํ ์ ์์ต๋๋ค.
์์ฉ ๊ธฐ์ : Pergolide acts as a potent, long-acting agonist at **D1 and D2 dopamine receptors** (estimated to be 10-1000 times more potent than bromocriptine). * **Mechanism in PPID:** In healthy horses, the hypothalamus releases dopamine, which tonically inhibits the pituitary pars intermedia. In horses with PPID, there is a neurodegenerative loss of these dopaminergic neurons. * **Pathway:** Pergolide replaces this lost dopamine tone โ binds to **D2 receptors** on melanotropes in the pars intermedia โ inhibits the hypersecretion of **pro-opiomelanocortin (POMC)** peptides (including ACTH, ฮฑ-MSH, and CLIP). * This reduction in POMC peptides normalizes endocrine function and alleviates the clinical signs associated with PPID.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Equine 'Cushing's-like' Disease [pituitary pars intermedia dysfunction (PPID)] ยท Initial dose of 1 mg (total dose) per day for horses and ponies with PPID. If the horse owner is willing to administer half the dose twice daily, this may be preferable on the basis of recent pharmacokinetic data. If anorexia or temporary dullness develop, treatment should be halted for 2 days or until appetite improves, and then restarted at 0.25 mg per day for 2 days, 0.5 mg per day for 2 days, and 0.75 mg per day for 2 days. ยท PO ยท q24h or divided q12h
- Equine 'Cushing's-like' Disease [pituitary pars intermedia dysfunction (PPID)] ยท 1.7-5.5 micrograms/kg ยท PO ยท Varies ยท Dose varies considerably. The higher doses are used in the more advanced cases or those refractory to treatment at a lower dose.
- Equine 'Cushing's-like' Disease [pituitary pars intermedia dysfunction (PPID)] ยท 0.002 mg/kg. If no improvement is noted within 8-12 weeks, the daily dose can be increased by 0.002 mg/kg monthly up to a total dose of 0.006 mg/kg (3 mg/day for a 500 kg horse). If only a limited response is observed with 0.006 mg/kg dose, addition of cyproheptadine (0.5 mg/kg PO q12h) to pergolide therapy is recommended. ยท PO ยท q24h ยท Usually, only transient anorexia is recognized during the initial week of treatment and can be overcome in time or by cutting the dose in half for 2-4 days.
์ฉ๋์ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์ฐธ๊ณ ์๋ฃ์ ๋๋ค. ํญ์ ์ต์ ๋ผ๋ฒจ๊ณผ ๊ฐ๋ณ ํ์์ ๋ํด ํ์ธํ์ญ์์ค.
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Hypersensitivity to pergolide or other ergot derivatives
์ด์๋ฐ์
- Anorexia/decreased appetite (up to 10% of horses during the first week)
- Colic (rare)
- Diarrhea (rare)
- Lethargy (dogs)
- Vomiting (dogs)
- Hypertension (dogs)
- Ptosis (dogs)
์ฝ๋ฌผ ์ํธ์์ฉ
- Dopamine antagonists (e.g., phenothiazines) ยท May decrease the effects of pergolide
- Metoclopramide ยท May decrease the effects of pergolide
๋ชจ๋ํฐ๋ง
- Dexamethasone suppression test (baseline and at 4-8 weeks post pergolide therapy initiation, repeat in 4-8 weeks if dosage is adjusted)
- Blood glucose (baseline, and if abnormal repeat as per dexamethasone suppression test)
- Clinical signs (hair coat, weight, PU/PD, etc.)
- Periodic CBC and clinical chemistry panel
๊ณผ์ฉ๋
Limited information is available on pergolide overdoses. * **Potential effects:** GI disturbances, CNS effects, seizures, and hypotension. * **Dogs:** Accidental ingestion has resulted in vomiting, lethargy, hypertension, and ptosis. * **Treatment:** Care is primarily supportive. Phenothiazines (dopamine antagonists) may be used to decrease CNS stimulation effects.
VetSheet ์ฝ๋ฌผ ๋ ํผ๋ฐ์ค๋ ๋ฉดํ ์์ ์ ๋ฌธ๊ฐ๋ฅผ ์ํ ์์ ์์ฌ๊ฒฐ์ ๋ณด์กฐ ๋๊ตฌ์ด๋ฉฐ, ์ ๋ฌธ์ ํ๋จ์ด๋ ์ ์กฐ์ฌ์ ์ต์ ๋ผ๋ฒจ์ ๋์ ํ์ง ์์ต๋๋ค.