์์ฐ (์์ธํธ์ฐ ์์ฐ, ํฉ์ฐ ์์ฐ, ๊ธ๋ฃจ์ฝ์ฐ ์์ฐ)
์์ฐ์ ํ์ ๋ฏธ๋ ์์์ด์ ์์์ ๋ก, ์ฒด๋ด 200๊ฐ ์ด์์ ๊ธ์ํจ์ ๊ธฐ๋ฅ์ ๋งค์ฐ ์ค์ํฉ๋๋ค. ์ธํฌ๋ง๊ณผ ํต์ฐ์ ๊ตฌ์กฐ์ ์์ ์ฑ์ ์ ์งํ๋ ๋ฐ ์ค์ํ ์ญํ ์ ํ๋ฉฐ, ์ธํฌ ์ฑ์ฅ, ๋ฉด์ญ ๋ฐ์, ์์ฒ ์น์ ๋ฐ ์๋ ฅ์ ํ์ํฉ๋๋ค. ์์ํ์์ ์์ฐ์ ์ฃผ๋ก ๋ค์ ์ฉ๋๋ก ์ฌ์ฉ๋ฉ๋๋ค: * **์์ฐ ๋ฐ์์ฑ ํผ๋ถ์ผ**: * *์ 1ํ*: ์ฃผ๋ก ๋ถ๋ฐฉ๊ฒฌ์ข (์: ์๋ฒ ๋ฆฌ์ ํ์คํค, ์๋์ค์นธ ๋ง๋ผ๋ฎคํธ)์์ ๋ํ๋๋ ์์ฐ ํก์์ ์ ์ ์ ๊ฒฐํจ. * *์ 2ํ*: ํผํธ์ฐ์ด๋ ์นผ์์ด ๋ง์ ์๋จ์ ์ญ์ทจํ ๊ธ์ฑ์ฅํ๋ ๋ํ๊ฒฌ ๊ฐ์์ง์์ ๋ฐ์ํ๋ฉฐ, ์ด ์ฑ๋ถ๋ค์ด ์์ด ์์ฐ๊ณผ ๊ฒฐํฉํ์ฌ ํก์๋ฅผ ๋ฐฉํดํฉ๋๋ค. * **๊ฐ ๊ตฌ๋ฆฌ ์ค๋ ์ฆ**: ์ทจ์ฝํ ํ์ข (์: ๋ฒ ๋ค๋งํด ํ ๋ฆฌ์ด, ์จ์คํธ ํ์ผ๋๋ ํ์ดํธ ํ ๋ฆฌ์ด, ๋๋ธ๋ผ๋ ๋ฆฌํธ๋ฆฌ๋ฒ)์์ ์ฅ๋ด ๊ตฌ๋ฆฌ ํก์๋ฅผ ์ฐจ๋จํ๊ธฐ ์ํด ์ฌ์ฉ๋ฉ๋๋ค. * **๊ฐ ์ฌ์ ์ฆ ๋ฐ ์ง๋ฐฉ๊ฐ**: ๋ณด์กฐ์ ์ธ ๊ฐ ๋ณดํธ ๋ฐ ํญ์ฌ์ ํ์ ๋ก ์ฌ์ฉ๋ฉ๋๋ค. > **์์ ํ**: ์ฉ๋์ ๊ณ์ฐํ ๋ **์์ ์์ฐ(elemental zinc)**๊ณผ **์์ฐ์ผ(zinc salts)**์ ๊ตฌ๋ณํ๋ ๊ฒ์ด ๋งค์ฐ ์ค์ํฉ๋๋ค. ์๋ฅผ ๋ค์ด, ํฉ์ฐ ์์ฐ์๋ 23%์ ์์ ์์ฐ์ด ํฌํจ๋์ด ์์ง๋ง, ๊ธ๋ฃจ์ฝ์ฐ ์์ฐ์๋ 14.3%๋ง ํฌํจ๋์ด ์์ต๋๋ค. ํฌ์ฌ ํ๋กํ ์ฝ์ด ์ด๋ค ํํ๋ฅผ ๊ธฐ์ค์ผ๋ก ํ๋์ง ํญ์ ํ์ธํ์ญ์์ค.
์์ฉ ๊ธฐ์ : Zinc acts as a critical cofactor for numerous metalloenzymes, including **alkaline phosphatase**, **alcohol dehydrogenase**, **carbonic anhydrase**, and **RNA polymerase**. **Mechanism in Copper Toxicosis**: When administered orally in large doses, zinc induces the synthesis of **metallothionein** in intestinal enterocytes. Metallothionein is a cysteine-rich protein that has a much higher binding affinity for copper than for zinc. Dietary zinc โ Induces enterocyte metallothionein โ Binds dietary and biliary copper โ Traps copper within the enterocyte โ Enterocyte is sloughed into the feces (normal turnover) โ **Negative copper balance**.
๋๋ฌผ ์ข ๋ณ ์ฉ๋
- Adjunctive therapy of severe hepatic lipidosis ยท 7-10 mg/kg PO once daily, in B-Complex mixture if possible ยท PO ยท q24h
- Appetite stimulant ยท 1 mg/kg of elemental zinc PO once a day ยท PO ยท q24h
- Zinc-responsive dermatoses, copper storage disease ยท 1-2 mg elemental zinc p.o. q24h (zinc sulphate: 5 mg/kg p.o. q24h or in divided doses; zinc gluconate: 2 mg/kg p.o. q24h; zinc acetate: 1 mg/kg p.o. q24h) ยท PO ยท q24h ยท Not specified ยท Give with food to minimize vomiting.
- Adjunctive treatment and prophylaxis of hepatic copper toxicosis ยท Initially, give a loading dose of 100 mg elemental zinc (zinc acetate used in this study) twice daily (separate doses by at least 8 hours) for about 3 months; then reduce dose to 50 mg (elemental zinc) twice daily. ยท PO ยท q12h ยท Lifetime/Maintenance ยท If animal vomits, give doses with a small piece of meat. Do not give within one hour of a meal. Target zinc levels are 200-500 micrograms/dL.
- Adjunctive treatment and prophylaxis of hepatic copper toxicosis ยท 5-10 mg/kg elemental zinc q12h; use high end of dosage range initially for 3 months, then 50 mg PO q12h for maintenance. ยท PO ยท q12h ยท Lifetime/Maintenance ยท Separate dosage from meals by 1-2 hours. In dogs with active copper-induced hepatitis, do not use zinc alone, but in combination with a chelator.
- Adjunctive treatment and prophylaxis of hepatic copper toxicosis ยท 10 mg/kg elemental zinc (given as zinc acetate or zinc gluconate) PO twice daily. ยท PO ยท q12h ยท Give one hour before each meal.
- Adjunctive treatment and prophylaxis of hepatic copper toxicosis ยท 1.5-2.5 mg/kg zinc gluconate PO three times daily; 0.67 mg/kg zinc sulfate PO three times daily; or 100 mg (total dose) elemental zinc (as zinc acetate) PO twice daily. ยท PO ยท q8h or q12h ยท 3-6 month loading, then half dose ยท Goal is to achieve zinc plasma concentrations of 200-600 micrograms/dL.
ํฌ์ฌ ๊ฒฝ๋ก
๊ธ๊ธฐ
- Patients with pre-existing copper deficiency
- Patients with copper deficiency
์ด์๋ฐ์
- Gastrointestinal disturbances (vomiting, nausea, anorexia)
- Hematologic abnormalities (hemolytic anemia, particularly at serum levels >1000 mcg/dL)
- Hypotension (with overdose)
- Jaundice (with overdose)
- Pulmonary edema (with overdose)
- Nausea
- Vomiting
- Diarrhoea
- Haemolysis (at high doses)
์ฝ๋ฌผ ์ํธ์์ฉ
- Copper ยท Large doses of zinc inhibit copper absorption in the intestine; separate supplements by at least 2 hours. ยท moderate
- Fluoroquinolones (e.g., enrofloxacin, ciprofloxacin) ยท Zinc salts may reduce the oral absorption of fluoroquinolones.
- Penicillamine ยท May potentially inhibit zinc absorption; clinical significance is not clear. ยท minor
- Tetracyclines ยท Zinc salts may chelate oral tetracycline and reduce its absorption; separate doses by at least 2 hours. ยท major
- Ursodiol ยท May potentially inhibit zinc absorption; clinical significance is not clear.
- Iron ยท Long-term administration of zinc may lead to decreased iron stores and functional deficiency ยท moderate
- Ursodeoxycholic acid ยท May potentially inhibit zinc absorption ยท minor
- Fluoroquinolones ยท Zinc salts may reduce the absorption of fluoroquinolone antibiotics ยท major
๋ชจ๋ํฐ๋ง
- Serum zinc levels (Target 200-500 mcg/dL for copper toxicosis; do not exceed 1000 mcg/dL)
- Gastrointestinal signs (vomiting, anorexia)
- Complete Blood Count (CBC) to monitor for hemolysis/anemia
- Clinical response (resolution of dermatosis or hepatic signs)
- Serum zinc levels
- Serum copper levels
- Complete Blood Count (CBC) / PCV to monitor for haemolysis
๊ณผ์ฉ๋
Signs associated with overdoses of zinc in mammals include **hemolytic anemia**, hypotension, jaundice, vomiting, and pulmonary edema. > **Toxicity Alert**: Ingestion of U.S. pennies minted after 1982 is a common cause of severe zinc toxicosis in dogs, as these coins are 97.5% zinc. **Treatment in Mammals**: * Remove the source (e.g., endoscopic or surgical removal of coins). * Dilution with milk or water. * Chelation therapy using edetate calcium disodium (Calcium EDTA). **Avian Toxicity**: Zinc intoxication in birds is relatively common (often from cage wire or hardware). Clinical signs are varied and nonspecific: lethargy, anorexia, regurgitation, polyuria, polydipsia, hematuria, hematochezia, pallor, dark or bright green diarrhea, foul-smelling feces, paresis, seizures, and sudden death. Treatment involves removing the source, chelation therapy (Calcium EDTA or succimer), and supportive care.
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