Dendrobium nobile Lindl alkaloid attenuates 6-OHDA-induced dopamine neurotoxicity

Biotechnol Appl Biochem. 2021 Dec;68(6):1501-1507. doi: 10.1002/bab.2071. Epub 2020 Nov 17.

Abstract

Parkinson's disease (PD) is one of the most common central nervous system (CNS) degenerative disease and is characterized by a progressive loss of midbrain substantia nigra dopamine (DA) neurons. Dendrobium nobileLindl alkaloid (DNLA) is an active component extracted from D. nobile Lindl, which is a traditional Chinese herb. The various pharmacological effects of D. nobile are beneficial for human health. Recently, DNLA-mediated neuroprotective effects have been reported. However, the neuroprotection of DNLA on 6-hydroxydopamine (6-OHDA)-induced DA neurotoxicity is still unknown. This study aimed to explore the neuroprotective effects of DNLA on DA neurotoxicity induced by 6-OHDA. In PD rat model, continuous intragastric administration of DNLA (20 mg/kg) for 7 days significantly ameliorated 6-OHDA-induced DA neurons loss in the midbrain substantia nigra. In addition, primary rat midbrain neuron-glia cocultures were used to explore the mechanisms underlying DNLA-related DA neuroprotection. The studies on neuron-glia cocultures revealed that neuroprotective effects of DNLA (2.5 ng/mL) were mediated by inhibiting the release of proinflammatory cytokines. Taken together, DNLA holds neuroprotective effect on 6-OHDA-induced neurons neurodegeneration by selectively inhibiting the production of proinflammatory factors and could be a potential compound for PD treatment.

Keywords: 6-OHDA; DNLA; Parkinson's disease; dopamine neurotoxicity.

MeSH terms

  • Alkaloids / administration & dosage
  • Alkaloids / pharmacology*
  • Animals
  • Dopamine / toxicity
  • Male
  • Neurons / drug effects*
  • Neurons / pathology
  • Neuroprotective Agents / administration & dosage
  • Neuroprotective Agents / pharmacology*
  • Oxidopamine / antagonists & inhibitors*
  • Oxidopamine / pharmacology
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Alkaloids
  • Neuroprotective Agents
  • Oxidopamine
  • Dopamine