Oral Administration of Lipopolysaccharide Prevents Cognitive Impairment in Streptozotocin-induced Diabetic Mice in a Blood Glucose-independent Manner

Anticancer Res. 2021 Aug;41(8):4053-4059. doi: 10.21873/anticanres.15206.

Abstract

Background/aim: Diabetes is a risk factor for dementia. However, no radical preventive method for diabetes-associated dementia has yet been developed. Our previous study revealed that oral administration of lipopolysaccharide (LPS) prevents high-fat diet-induced cognitive impairment. Therefore, we investigated here whether oral administration of LPS (OAL) could also prevent diabetes-associated dementia.

Materials and methods: Diabetic mice were produced by intraperitoneal administration of streptozotocin (STZ), and then mice were orally administered LPS. Cognitive ability was evaluated using the Morris water maze, and gene expression was analyzed in isolated microglia.

Results: OAL prevented STZ-induced diabetic cognitive impairment, but did not affect blood glucose levels. Moreover, OAL promoted the expression of neuroprotective genes in microglia, such as heat shock protein family 40 (HSP40) and chemokine CCL7.

Conclusion: OAL prevents diabetes-associated dementia, potentially via promotion of HSP40 and CCL7 expression in microglia.

Keywords: Lipopolysaccharide (LPS); cognitive impairment; dementia; diabetes; microglia; oral administration; streptozotocin (STZ).

MeSH terms

  • Administration, Oral
  • Animals
  • Blood Glucose / drug effects
  • Chemokine CCL7 / genetics
  • Cognitive Dysfunction / blood
  • Cognitive Dysfunction / etiology
  • Cognitive Dysfunction / genetics
  • Cognitive Dysfunction / prevention & control*
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / drug therapy*
  • Diabetes Mellitus, Type 1 / genetics
  • HSP40 Heat-Shock Proteins / genetics
  • Lipopolysaccharides / pharmacology
  • Lipopolysaccharides / therapeutic use*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microglia / drug effects
  • Microglia / metabolism
  • Neuroprotective Agents / pharmacology
  • Neuroprotective Agents / therapeutic use*

Substances

  • Blood Glucose
  • Ccl7 protein, mouse
  • Chemokine CCL7
  • Dnajb1 protein, mouse
  • HSP40 Heat-Shock Proteins
  • Lipopolysaccharides
  • Neuroprotective Agents