AI Article Synopsis

  • Membrane transporters in the choroid plexus facilitate the movement of substances between blood and cerebrospinal fluid (CSF), with OCTN1 (SLC22A4) being a key transporter whose roles in this process are not fully understood.
  • In a study, tritium-labeled ergothioneine (labeled as [H]ERGO) was injected into mice to investigate OCTN1's function in clearing substances from the CSF.
  • Results showed that while wild-type mice efficiently cleared [H]ERGO from CSF, knockout mice lacking the octn1 gene had significantly reduced clearance, indicating that OCTN1 plays a vital role in removing ergothioneine from CSF in

Article Abstract

Membrane transporters expressed in the choroid plexus (CP) are involved in the transport of substances between the blood and cerebrospinal fluid (CSF). Carnitine/organic cation transporter 1 (OCTN1, also known as SLC22A4) is expressed in rodent CP; however, its specific roles in blood-CSF transport remain unclear. Therefore, in this study, we aimed to evaluate the potential role of OCTN1 in the elimination of substances from CSF. Tritium-labeled ergothioneine ([H]ERGO), a typical in vivo substrate of OCTN1, was injected into the lateral ventricles of wild-type and octn1 gene knockout (octn1) mice. Clearance of [H]ERGO from CSF was higher than that of the bulk flow marker, [C]mannitol, in wild-type mice. However, [H]ERGO clearance was significantly lower in octn1 mice than in wild-type mice. Furthermore, OCTN1 expression in CP was determined via immunohistochemical analysis. CP/CSF ratio of [H]ERGO was significantly lower in octn1 mice than in wild-type mice. These results suggest that OCTN1 is functionally expressed in CP and involved in the elimination of ERGO from CSF in mice.

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Source
http://dx.doi.org/10.1248/bpb.b24-00451DOI Listing

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