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Published on: March 11, 2016
Tissue distribution and renal developmental changes in rat organic cation transporter mRNA levels
A L Slitt1, N J Cherrington, D P Hartley
1Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas, USA.
Abstract:
Organic cation transporters (OCTs) are responsible for excretion of cationic substances into urine. Tissue OCT expression may be important for the disposition and excretion of xenobiotics. Therefore, OCT1, OCT2, OCT3, OCTN1, and OCTN2 mRNA levels were measured in adult rat tissues and rat kidney tissue at various stages of development from day 0 to 45. OCT1 mRNA expression was highest in kidney and spleen, moderate in skin, and low in the gastrointestinal tract, brain, lung, thymus, muscle, and prostate. OCT2 mRNA levels were highest in kidney, with low expression in other tissues, and with renal OCT2 levels being approximately 4 times higher in males than that in females. In gonadectomized males, OCT2 mRNA levels were attenuated to female levels, suggesting a role for testosterone in OCT2 expression. OCT3 was moderately expressed in kidney and was highest in blood vessel, skin, and thymus. OCTN1 was expressed in most of the tissues examined, with relatively higher expression in kidney and ileum and lower levels in thymus. Lastly, OCTN2 was expressed abundantly in kidney and ileum, moderately in large intestine, dorsal prostate, bladder, duodenum, and cerebellum, and minimally in thymus, spleen, and cerebral cortex. Renal OCT1, OCTN1, and OCTN2 mRNA levels increased gradually from postnatal day 0 through day 45 in both genders. Renal OCT2 levels remained the same in males and females through day 25 and then dramatically increased only in male kidney after day 30. In summary, OCT mRNA was detected primarily in kidney, and the high level of renal OCT expression may explain why the kidney is a target organ for xenobiotics with cationic properties.
Insights
Organic cation transporters (OCTs) are crucial for excreting cationic substances. This study reveals significant OCT mRNA expression in rat kidneys, highlighting their role in xenobiotic processing.
Area of Science:
- Pharmacology
- Molecular Biology
- Physiology
Background:
- Organic cation transporters (OCTs) facilitate the excretion of cationic compounds.
- Tissue-specific OCT expression influences the disposition and elimination of xenobiotics.
- Understanding OCT distribution is vital for predicting drug and toxin behavior.
Purpose of the Study:
- To quantify mRNA levels of OCT1, OCT2, OCT3, OCTN1, and OCTN2 in adult rat tissues.
- To examine the developmental expression of renal OCTs from postnatal day 0 to 45.
- To investigate the influence of sex and gonadectomy on OCT2 expression.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) was used to measure OCT mRNA expression.
- Analysis was performed on various adult rat tissues.
- Kidney tissues from rats at different developmental stages (postnatal days 0-45) were analyzed.
Main Results:
- OCT1, OCT2, OCT3, OCTN1, and OCTN2 mRNA were detected in multiple rat tissues, with prominent expression in the kidney.
- Renal OCT1, OCTN1, and OCTN2 mRNA levels increased developmentally in both sexes.
- Renal OCT2 expression was significantly higher in adult males, influenced by testosterone, and showed a distinct postnatal surge after day 30 in males.
Conclusions:
- The kidney exhibits substantial expression of multiple OCT family members, underscoring its importance in handling cationic xenobiotics.
- Developmental and sex-specific expression patterns, particularly for OCT2, suggest complex regulatory mechanisms.
- These findings provide a foundation for understanding the renal handling of cationic drugs and endogenous compounds.
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