Anti-Amnesic Effect of Agastache rugosa on Scopolamine-Induced Memory Impairment in Miceopen access
- Authors
- Kang, Sohi; Lee, Nari; Jung, Bokyung; Jeong, Huiyeong; Moon, Changjong; Park, Sang-Ik; Yun, Seungpil; Yim, Teresa; Oh, Jung Min; Kim, Jae-Won; Song, Ji Hoon; Chae, Sungwook; Kim, Joong Sun
- Issue Date
- Sep-2024
- Publisher
- Multidisciplinary Digital Publishing Institute (MDPI)
- Keywords
- Agastache rugosa; cholinergic system dysfunction; cognitive dysfunction; neuroprotection; scopolamine hydrobromide
- Citation
- Pharmaceuticals, v.17, no.9
- Indexed
- SCIE
SCOPUS
- Journal Title
- Pharmaceuticals
- Volume
- 17
- Number
- 9
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/74346
- DOI
- 10.3390/ph17091173
- ISSN
- 1424-8247
1424-8247
- Abstract
- Agastache rugosa, a traditional Asian herbal medicine, is primarily used for digestive problems; yet, its cognitive benefits remain unexplored. This study evaluated the anti-amnesic effects of A. rugosa extract (ARE) on scopolamine (SCO)-induced memory impairment in mice. Mice received 100 or 200 mg/kg ARE orally for 5 days, followed by SCO injection. The ARE demonstrated significant antioxidant (DPPH IC50: 75.3 µg/mL) and anti-inflammatory effects (NO reduction). Furthermore, the ARE significantly improved memory performance in the passive avoidance test (escape latency: 157.2 s vs. 536.9 s), the novel object recognition test (novel object preference: 47.6% vs. 66.3%) and the Morris water maze (time spent in the target quadrant: 30.0% vs. 45.1%). The ARE reduced hippocampal acetylcholinesterase activity (1.8-fold vs. 1.1-fold) while increasing choline acetyltransferase (0.4-fold vs. 1.0-fold) and muscarinic acetylcholine receptor subtype I (0.3-fold vs. 1.6-fold) expression. The ARE improved hippocampal neurogenesis via doublecortin- (0.4-fold vs. 1.1-fold) and KI-67-positive (6.3 vs. 12.0) cells. Therefore, the ARE exerts protective effects against cognitive decline through cholinergic system modulation and antioxidant activity, supporting its potential use as a cognitive enhancer. © 2024 by the authors.
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