Korean J Physiol Pharmacol.  2012 Apr;16(2):79-89. 10.4196/kjpp.2012.16.2.79.

Phellodendron amurense and Its Major Alkaloid Compound, Berberine Ameliorates Scopolamine-Induced Neuronal Impairment and Memory Dysfunction in Rats

Affiliations
  • 1Acupuncture and Meridian Science Research Center, College of Oriental Medicine, Kyung Hee University, Seoul 130-701, Korea. bombi@khu.ac.kr, dhhahm@khu.ac.kr
  • 2The Graduate School of Basic Science of Oriental Medicine, College of Oriental Medicine, Kyung Hee University, Seoul 130-701, Korea.

Abstract

We examine whether Phellodendron amurense (PA) and its major alkaloid compound, berberine (BER), improved memory defects caused by administering scopolamine in rats. Effects of PA and BER on the acetylcholinergic system and pro-inflammatory cytokines in the hippocampus were also investigated. Male rats were administered daily doses for 14 days of PA (100 and 200 mg/kg, i.p.) and BER (20 mg/kg, i.p.) 30 min before scopolamine injection (2 mg/kg, i.p.). Daily administration of PA and BER improved memory impairment as measured by the passive avoidance test and reduced the escape latency for finding the platform in the Morris water maze test. Administration of PA and BER significantly alleviated memory-associated decreases in cholinergic immunoreactivity and restored brain-derived neurotrophic factor and cAMP-response element-binding protein mRNA expression in the hippocampus. PA and BER also decreased significantly the expression of proinflammatory cytokines such as interleukin-1beta, tumor necrosis factor-alpha and cyclooxygenase-2 mRNA in the hippocampus. These results demonstrated that PA and BER had significant neuroprotective effects against neuronal impairment and memory dysfunction caused by scopolamine in rats. These results suggest that PA and BER may be useful as therapeutic agents for improving cognitive functioning by stimulating cholinergic enzyme activity and alleviating inflammatory responses.

Keyword

Scopolamine; Memory; Cholinergic neurons; Brain-derived neurotrophic factor; Proinflammatory cytokines

MeSH Terms

Animals
Berberine
Brain-Derived Neurotrophic Factor
Cholinergic Neurons
Cyclooxygenase 2
Cytokines
Hippocampus
Humans
Interleukin-1beta
Male
Memory
Neurons
Neuroprotective Agents
Phellodendron
Rats
RNA, Messenger
Scopolamine Hydrobromide
Tumor Necrosis Factor-alpha
United Nations
Berberine
Brain-Derived Neurotrophic Factor
Cyclooxygenase 2
Cytokines
Interleukin-1beta
Neuroprotective Agents
RNA, Messenger
Scopolamine Hydrobromide
Tumor Necrosis Factor-alpha

Figure

  • Fig. 1 Experimental schedules of scopolamine-induced spatial memory impairments in the rats. Exp 1 was designed to explore the efficacy of PA and BER administration for amelioration of memory impairment in an animal model using a passive avoidance test (PAT) and immunohistochemistry. Exp 2 was designed to explore the efficacy of PA and BER administration for amelioration of memory impairment in an animal model using the Morris water maze (MWM) test, ELISA and RT-RCT analyses.

  • Fig. 2 Effect of PA and BER on the latencies to enter the dark compartment in the acquisition trial and in the retention test during the PAT test. ***p<0.001 vs. the SAL group; #p<0.05 and ##p<0.01 vs. the SCO group.

  • Fig. 3 Time to escape (latency) during acquisition trials of hidden platform (A), probe trial (B), and swim speed (C) during the Morris water maze test. **p<0.01 and ***p<0.001 vs. the SAL group; #p<0.05 and ##p<0.01 vs. the SCO group.

  • Fig. 4 Representative photographs showing the distribution of choline acetyltransferase- and acetylcholinesterase-reactive cells in the hippocampus of the SAL-ChAT-MS (A), SCO-ChAT-MS (B), SCO+PA200-ChAT-MS (C), SAL-ChAT-hippocampus (D) SCO-ChAT-hippocampus (E), SCO+PA200-ChAT-hippocampus (F), SAL-AchE-CA1 (G), SCO-AchE-CA1 (H), SCO+PA200-AchE-CA1 (I), SAL-AchE-CA1 (J), SCO-AchE-CA1 (K), and SCO+PA200-AchE-CA1 (L) groups. Sections were cut coronally at 30 µm. Scale bar indicates 50 µm.

  • Fig. 5 Percentage (±SE) values of the mean number of choline acetyltransferase (ChAT)-stained neurons (A) and the density of acetylcholinesterase-stained neuron (B) in different hippocampal areas after the Morris water maze task. **p<0.01 and ***p<0.001 vs. the SAL group; #p<0.05 and ##p<0.01 vs. the SCO group.

  • Fig. 6 Interleukin-1 beta (IL-1β) (A) and Interleukin-6 (IL-6) (B) protein expression in rat plasma after scopolamine injection for 14 days. *p<0.05 and **p<0.01 vs. the SAL group; #p<0.05 vs. the SCO group.

  • Fig. 7 PCR bands and their relative intensities of brain-derived neurotrophic factor (BDNF) and cAMP-response element-binding protein (CREB) mRNA (A), and PCR bands and their relative intensities of interleukin-1 beta (IL-1β), tumour necrosis factor (TNF)-α, and cyclooxygenase-2 (COX-2) mRNA (B) in the hippocampus of scopolamine-induced cognitive impairment rats. *p<0.05 and **p<0.01 vs. the SAL group; #p<0.05 and ##p<0.01 vs. the SCO group.


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