Anti-Amnesic Effect of Agastache rugosa on Scopolamine-Induced Memory Impairment in Mice

Author:

Kang Sohi12ORCID,Lee Nari3,Jung Bokyung1,Jeong Huiyeong1,Moon Changjong1ORCID,Park Sang-Ik1ORCID,Yun Seungpil4ORCID,Yim Teresa5,Oh Jung Min3,Kim Jae-Won3,Song Ji Hoon36,Chae Sungwook78,Kim Joong Sun1

Affiliation:

1. College of Veterinary Medicine and BK21 FOUR Program, Chonnam National University, Gwangju 61186, Republic of Korea

2. Department of Anatomy and Convergence Medical Science, College of Medicine, Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Republic of Korea

3. Jeju Institute of Korean Medicine, Jeju-si 63309, Republic of Korea

4. Department of Pharmacology and Convergence Medical Science, College of Medicine, Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Republic of Korea

5. Global GreenFriends Co., Seocho-gu, Seoul 06569, Republic of Korea

6. Vital to Life Co., Seongnam-si 13306, Republic of Korea

7. Center for Companion Animal New Drug Development, Jeonbuk Branch, Korea Institute of Toxicology, Jeongeup 56212, Republic of Korea

8. KMConvergence Research Division, Korea Institute of Oriental Medicine, 1672 Yuseongdae-ro, Yuseong-gu, Daejeon 34054, Republic of Korea

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.

Funder

Gyeongsang National University in 2024

Regional Innovation Strategy (RIS) through the National Research Foundation of Korea funded by the Ministry of Education

Convergence Research Group Project of the National Research Council of Science

Technology Development Program of MSS

Publisher

MDPI AG

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