MDR1 Mutation
ABCB1 gene mutation
Cunoscută și ca: ABCB1 Mutation, MDR1 Gene Defect, P-glycoprotein Deficiency
Pe scurt
The MDR1 mutation (ABCB1 gene defect) is a common hereditary condition in dogs, especially herding breeds, that causes life-threatening sensitivities to everyday medications. Learn how to identify at-risk dogs, recognize signs of drug toxicity, and safely manage your dog's healthcare with genetic testing.

TL;DR. O mutație genetică frecventă la rasele de păstorit dezactivează o proteină protectoare și face medicamente uzuale toxice sau fatale.
Shetland Sheepdogs are among the herding breeds highly predisposed to the MDR1 mutation.
Ce este?
The MDR1 (ABCB1) mutation is a hereditary defect that impairs P-glycoprotein, an efflux pump concentrated at the blood-brain barrier and in liver, kidney, and gut. Without a working pump, many drugs accumulate in sensitive tissues and cause neurologic or organ toxicity at ordinary doses.
Cauze și factori de risc
Autosomal incomplete dominant inheritance. Homozygous mutants lack functional P-glycoprotein; heterozygous carriers have reduced capacity and can still react at higher doses. Risk is breed-linked: Collie, Shetland Sheepdog, Australian Shepherd, Miniature American Shepherd, German Shepherd, Old English Sheepdog, Border Collie, English Shepherd, Whippet, Longhaired Whippet, Silken Windhound, and mixes with herding ancestry.
Semne
- Vomiting, ataxia, lethargy, tremors, hypersalivation
- Depression, anorexia, mydriasis, diarrhea
- Bone marrow suppression (chemo substrates)
- Occasional: tachycardia, dehydration, seizures
"Common findings in dogs recorded in decreasing frequency included vomiting, ataxia, lethargy, tachycardia, hypersalivation, mydriasis, and seizures." - Plumb's Veterinary Drug Handbook, p.1982

Dilated pupils and severe lethargy are common clinical signs of drug toxicity in MDR1-affected dogs.
Cum diagnostichează medicii veterinari
One-time MDR1 genetic testing (cheek swab or blood) classifies clear, carrier, or affected. In acute toxicity: history of drug exposure, neurologic exam, CBC/chemistry for organ support and marrow effects.

Intravenous fat emulsion (lipid rescue therapy) is used to reverse severe lipophilic drug toxicities.
Opțiuni de tratament
No cure for the genotype. Acute exposure: decontamination if recent; Activated Charcoal; Intravenous Fat Emulsion for severe lipophilic toxicity (e.g. ivermectin); IV fluids, seizure control, intensive support. Lifelong: avoid or dose-adjust high-risk drugs (loperamide, high-dose ivermectin, some chemotherapeutics, acepromazine, butorphanol).
Prognostic
Excellent if never exposed to problem drugs. Guarded after high-dose toxicity depending on drug, dose, speed of care, and access to lipid rescue.
Prevenire
Test at-risk breeds and mixes before routine meds or chemo. Keep a contraindicated-drug list for every caretaker. Prefer MDR1-safe heartworm preventives when indicated.
Când sunați medicul veterinar
Emergency now: seizures, severe ataxia or inability to stand, stupor, non-reactive dilated pupils, uncontrolled drooling with vomiting after a suspect drug.
Pentru rase specifice
Highest prevalence reported in Collies; also common in Shelties, Australian Shepherds, and Miniature American Shepherds. Appearance alone does not predict status; DNA test once.
Surse
- Plumb's Veterinary Drug Handbook, pages 1280, 1982, 2140.
- Small Animal Internal Medicine (5th Edition), page 1178.
- Small Animal Critical Care Medicine (2nd Edition), page 993.
My highlights & notes
Semne și simptome
Rase cu risc mai mare
Cum se diagnostichează
- MDR1 Genetic TestingStandard de aur
Abordări de tratament
Tratamentul trebuie prescris de un medic veterinar autorizat. Dozele specifice nu sunt afișate intenționat.
Întrebări frecvente
What is MDR1 Mutation?
The MDR1 mutation (ABCB1 gene defect) is a common hereditary condition in dogs, especially herding breeds, that causes life-threatening sensitivities to everyday medications. Learn how to identify at-risk dogs, recognize signs of drug toxicity, and safely manage your dog's healthcare with genetic testing.
What are the symptoms of MDR1 Mutation?
Loss of appetite、Ataxia (wobbly, unsteady walking)、Low mood and dullness、Diarrhoea、Excessive drooling、Lethargy、Mydriasis、Tremors (shaking, trembling)
How is MDR1 Mutation diagnosed?
MDR1 Genetic Testing
How is MDR1 Mutation treated?
Tratamentul trebuie prescris de un medic veterinar autorizat. Dozele specifice nu sunt afișate intenționat.
Surse
- Plumb · p. 1982
- Internal Medicine 5th · p. 1178
- Small Animal Critical Care Medicine, 2nd Edition (VetBooks.ir) · p. 993
- Plumb · p. 2140
- Plumb · p. 1280
Acest articol este educație generală și nu înlocuiește sfatul veterinar. Dacă animalul e bolnav, consultați un veterinar.
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