Gintonin Attenuates D-Galactose-Induced Hippocampal Senescence by Improving Long-Term Hippocampal Potentiation, Neurogenesis, and Cognitive Functions

Gerontology. 2018;64(6):562-575. doi: 10.1159/000491113. Epub 2018 Aug 23.

Abstract

Background: Ginseng has been used to improve brain function and increase longevity. However, little is known about the ingredients of ginseng and molecular mechanisms of its anti-brain aging effects. Gintonin is a novel exogenous ginseng-derived lysophosphatidic acid (LPA) receptor ligand; LPA and LPA1 receptors are involved in adult hippocampal neurogenesis. D-galactose (D-gal) is used to induce brain -aging in animal models because long-term treatment with D-gal facilitates hippocampal aging in experimental adult animals by decreasing hippocampal neurogenesis and inducing learning and memory dysfunction.

Objective: To investigate the protective effects of gintonin on D-gal-induced hippocampal senescence, impairment of long-term potentiation (LTP), and memory dysfunction.

Methods: Brain hippocampal aging was induced by D-gal administration (150 mg/kg/day, s.c.; 10 weeks). From the 7th week, gintonin (50 or 100 mg/kg/day, per os) was co-administered with D-gal for 4 weeks. We performed histological analyses, LTP measurements, and object location test.

Results: Co-administration of gintonin ameliorated D-gal-induced reductions in hippocampal Ki67-immunoreactive proliferating cells, doublecortin-immunoreactive neuroblasts, 5-bromo-2'-deoxyuridine-incorporating NeuN-immunoreactive mature neurons, and LPA1 receptor expression. Co-administration of gintonin in D-gal-treated mice increased the expression of phosphorylated cyclic adenosine monophosphate response element binding protein in the hippocampal dentate gyrus. In addition, co-administration of gintonin in D-gal-treated mice enhanced LTP and restored the cognitive functions compared with those in mice treated with D-gal only.

Conclusion: These results show that gintonin administration restores D-gal-induced memory deficits by enhancing hippocampal LPA1 receptor expression, LTP, and neurogenesis. Finally, the present study shows that gintonin exerts anti-brain aging effects that are responsible for alleviating brain aging-related dysfunction.

Keywords: Anti-brain aging; Brain senescence; D-galactose; Ginseng; Gintonin; Hippocampus; Neurogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cellular Senescence* / drug effects
  • Cellular Senescence* / physiology
  • Disease Models, Animal
  • Galactose / metabolism*
  • Glycoproteins / pharmacology
  • Hippocampus* / drug effects
  • Hippocampus* / metabolism
  • Long-Term Potentiation / drug effects*
  • Lysophospholipids / pharmacology
  • Memory Disorders* / drug therapy
  • Memory Disorders* / metabolism
  • Memory Disorders* / physiopathology
  • Mice
  • Neurogenesis / drug effects
  • Neurons / drug effects
  • Neurons / physiology
  • Plant Extracts / pharmacology*
  • Receptors, Lysophosphatidic Acid / metabolism
  • Treatment Outcome

Substances

  • Glycoproteins
  • Lysophospholipids
  • Plant Extracts
  • Receptors, Lysophosphatidic Acid
  • gintonin
  • Galactose