HUREL® Rat WH™

Co-culture comprised of cryopreserved primary rat hepatocytes cultured with cells of non-parenchymal, stromal type.


Example Metabolic Activity (nmoles/hr/106 cells)

SubstrateEnzymeConcentration (µM)Day 1Day 4Day 8
7-EthoxycoumarinPhase I(ECOD)1000.050.050.05
Phase II(UGT)0.050.050.05
Phase II(SULT)0.050.050.05
7-HydroxycoumarinPhase II(UGT)1000.050.050.05
Phase II(SULT)0.050.050.05

Culture Conditions and Morphology

Cryopreserved human hepatocytes were thawed and plated with HUREL PlatinumHeps™ Media supplemented with 10% serum and subsequently changed 24 hours post-seeding to HUREL PlatinumHeps™ Basal Media. CYP substrate concentrations are given in the table above along with metabolite formation recorded as nmoles/hr/106 cells. All incubations were carried out in triplicate on days 1, 4, and 8 upon cell delivery and incubated for 60 minutes. Reactions took place in a humidified incubator at 37°C, in 5% CO2. Col­lected supernatants were stored at -20°C until further LC/MS/MS analysis.


Day 1 – Morphology

Day 7 – Morphology

Day 7 – Bile Canaliculi

Day 1- Morphology phase contrast image

Phase contrast image in a 24-well at a 10X magnification.

Day 7- Morphology phase contrast image

Phase contrast image in a 24-well at a 10X magnification.

Day 7- Bile Canaliculi assay

Bile canaliculi assayed via 5-(and-6)-carboxy-2′, 7′ – dichlorofluorescein diacetate (C-DCFDA) stain at a concentration of 5 microns and imaged in the GFP channel in a 96-well at 10X magnifcation with filters EX/EM 492-495/512-527 nm


Example Culture Origin

Rat Donor Demographics
  • Strain: Wister Han
  • Number of Donors:14
  • Age: 14 months
  • Gender: Male