PAN-811 prevents chemotherapy-induced cognitive impairment and preserves neurogenesis in the hippocampus of adult rats

PLoS One. 2018 Jan 25;13(1):e0191866. doi: 10.1371/journal.pone.0191866. eCollection 2018.

Abstract

Chemotherapy-induced cognitive impairment (CICI) occurs in a substantial proportion of treated cancer patients, with no drug currently available for its therapy. This study investigated whether PAN-811, a ribonucleotide reductase inhibitor, can reduce cognitive impairment and related suppression of neurogenesis following chemotherapy in an animal model. Young adult rats in Chemo and Chemo+PAN-811 groups received 3 intraperitoneal (i.p.) injections of methotrexate (MTX) and 5-fluorouracil (5-FU), and those in Saline and Saline+PAN-811 groups received equal volumes of physiological saline at 10-day intervals. PAN-811 in saline was delivered through i.p. injection, 10 min following each saline (Saline+PAN-811 group) or MTX/5-FU (Chemo+PAN-811 group) treatment, while equal volumes of saline were delivered to Saline and Chemo groups. Over Days 31-66, rats were administered tests of spatial memory, nonmatching-to-sample rule learning, and discrimination learning, which are sensitive to dysfunction in hippocampus, frontal lobe and striatum, respectively. On Day 97, neurogenesis was immnunohistochemically evaluated by counting doublecortin-positive (DCX+) cells in the dentate gyrus (DG). The results demonstrated that the Chemo group was impaired on the three cognitive tasks, but co-administration of PAN-811 significantly reduced all MTX/5-FU-induced cognitive impairments. In addition, MTX/5-FU reduced DCX+ cells to 67% of that in Saline control rats, an effect that was completely blocked by PAN-811 co-administration. Overall, we present the first evidence that PAN-811 protects cognitive functions and preserves neurogenesis from deleterious effects of MTX/5-FU. The current findings provide a basis for rapid clinical translation to determine the effect of PAN-811 on CICI in human.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / adverse effects
  • Cognitive Dysfunction / chemically induced
  • Cognitive Dysfunction / prevention & control*
  • Dentate Gyrus / drug effects
  • Discrimination Learning / drug effects
  • Disease Models, Animal
  • Doublecortin Protein
  • Enzyme Inhibitors / pharmacology
  • Female
  • Fluorouracil / administration & dosage
  • Fluorouracil / adverse effects
  • Hippocampus / drug effects
  • Hippocampus / pathology
  • Hippocampus / physiopathology
  • Humans
  • Learning / drug effects
  • Methotrexate / administration & dosage
  • Methotrexate / adverse effects
  • Neurogenesis / drug effects*
  • Neuroprotective Agents / pharmacology*
  • Pyridines / pharmacology*
  • Rats
  • Rats, Long-Evans
  • Ribonucleotide Reductases / antagonists & inhibitors
  • Spatial Memory / drug effects
  • Thiosemicarbazones / pharmacology*

Substances

  • Antineoplastic Agents
  • Dcx protein, rat
  • Doublecortin Protein
  • Enzyme Inhibitors
  • Neuroprotective Agents
  • Pyridines
  • Thiosemicarbazones
  • 3-aminopyridine-2-carboxaldehyde thiosemicarbazone
  • Ribonucleotide Reductases
  • Fluorouracil
  • Methotrexate

Grants and funding

Panacea Pharmaceuticals, Inc is a commercial company. We had submitted a patent of this concept, prior to this article. The funder provided support in the form of salaries for authors ZJ, SF and HAG, but the company as such did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘Author Contributions’ section.