Pharmacokinetics and distribution of 2-hydroxypropyl-β-cyclodextrin following a single intrathecal dose to cats

J Inherit Metab Dis. 2020 May;43(3):618-634. doi: 10.1002/jimd.12189. Epub 2019 Dec 15.

Abstract

2-Hydroxypropyl-β-cyclodextrin (HP-β-CD) is an experimental therapy for Niemann-Pick disease type C (NPC) that reduced neuronal cholesterol and ganglioside storage, reduced Purkinje cell death, and increased lifespan in npc1-/- mice and NPC1 cats. In this study, tissue distribution was investigated in normal cats that received a single 120-mg dose of [14 C]-HP-β-CD (approximately 200 μCi/cat) via the cerebellomedullary cistern (CBMC) and lumbar cistern. One cat was euthanized at each of various time points up to 24 hours postdose for subsequent processing and quantitative whole-body autoradiographic analysis. HP-β-CD-derived radioactivity absorbed from the CBMC was widely distributed to cat tissues; most tissues were observed to have reached their highest concentration at 1 hour postdose. HP-β-CD-derived radioactivity penetrated into the deeper parts of the central nervous system with the highest concentration at 4 hours (403 μg Eq/g or 0.28 mM) and remained high (49.7 μg Eq/g or 0.03 mM) at 24 hours. The relatively long half-life (11-30 hours) in cerebral ventricles and the subarachnoid space surrounding the brain and spinal cord might contribute to the efficacy of HP-β-CD in NPC1 cats. Other tissues with high concentrations of radioactivity were nasal turbinates, pituitary gland, and urinary bladder, while relatively low concentrations were observed in blood and bile.

Keywords: Niemann Pick type C; animal model; brain; cholesterol; drug therapy; inborn errors of metabolism; storage diseases.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2-Hydroxypropyl-beta-cyclodextrin / pharmacokinetics*
  • 2-Hydroxypropyl-beta-cyclodextrin / pharmacology*
  • Animals
  • Cats
  • Cholesterol / metabolism
  • Disease Models, Animal
  • Female
  • Male
  • Mice
  • Niemann-Pick C1 Protein / genetics*
  • Niemann-Pick Disease, Type C / drug therapy*
  • Niemann-Pick Disease, Type C / metabolism

Substances

  • Niemann-Pick C1 Protein
  • 2-Hydroxypropyl-beta-cyclodextrin
  • Cholesterol