Mdr1a-1b knockout rats
HsdSage:SD-Mdr1aem1SageMdr1bem1Sage
Location
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- Background strain: Sprague Dawley
- Mdr1a (Abcba1) and Mdr1b (Abc1b) have both been knocked out as a large deletion
Availability: Live colony
Zygosity genotype: Homozygous
P-glycoprotein plays a critical role in efflux for both brain and liver. Homozygous null Mdr1a rats display increased exposure to CNS drugs in the brain, as well as increased bioavailability in the plasma for P-gp-specific substrates.
MDR1 encodes for P-glycoprotein and is a membrane-bound drug transporter expressed in the brain and intestine. It effectively blocks drugs from crossing the blood-brain barrier. P-gp can confer multiple drug resistance to tumor cells. Absence of P-gp creates a functional deficiency in the blood-brain barrier and results in elevated drug levels in many tissues, making this a useful model for efflux assay, efficacy, formulation, tissue distribution, studying neurotoxicology and chemotherapeutic agents.
Origin:
The Mdr1a-1b KO rat model was originally created at SAGE Labs, Inc. in St. Louis, MO and distributed out of the Boyertown, PA facility. The line continues to be maintained through the original SAGE Labs animal inventory acquired by Envigo, then Envigo was acquired by Inotiv in 2021.
Diet and Husbandry:
Our rodent models are raised and maintained on Teklad diet, bedding, and enrichment products:
- Diet: Teklad Global Rodent Diet
- Bedding: Teklad Contact Bedding (U.S. only)
- Enrichment: Teklad Enrichment Products (U.S. only)
Model Support Services:
Inotiv offers related model support services to deliver research-ready models to your facility:
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Available regions:
For pricing information, please contact us using the phone number above.
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Research use and related publications
- Drug-drug interactions
- ADMET
- Blood brain barrier efflux
- DMPK assay
- Drug metabolism
- Drug resistance
- Drug transporter
- Efficacy
- Formulation drug-drug interactions
- Neurotoxicology
- PK-PD efflux assay