Planta Med 2019; 85(13): 1080-1087
DOI: 10.1055/a-0978-5214
Biological and Pharmacological Activity
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Acanthopanax senticosus Induces Vasorelaxation via Endothelial Nitric Oxide-Dependent and -Independent Pathways

Yayoi Shiokawa
1   Department of Pharmacology II, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Womenʼs University, Nishinomiya, Japan
,
Shino Miyauchi-Wakuda
1   Department of Pharmacology II, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Womenʼs University, Nishinomiya, Japan
,
Satomi Kagota
1   Department of Pharmacology II, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Womenʼs University, Nishinomiya, Japan
,
Kana Maruyama-Fumoto
1   Department of Pharmacology II, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Womenʼs University, Nishinomiya, Japan
,
Shizuo Yamada
2   Center for Pharma-Food Research, Graduate School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan
,
Kazumasa Shinozuka
1   Department of Pharmacology II, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Womenʼs University, Nishinomiya, Japan
› Author Affiliations
Further Information

Publication History

received 26 April 2019
revised 09 July 2019

accepted 11 July 2019

Publication Date:
23 July 2019 (online)

Abstract

Although Acanthopanax senticosus root extract (ASRE), a functional food used in Japan, improves peripheral blood circulation and exerts vasorelaxant effects in rats under healthy conditions, the underlying mechanisms currently remain unclear. Therefore, we investigated the mechanisms responsible for ASRE-induced relaxation in isolated thoracic aortas using organ bath techniques and examined whether ASRE affects systemic and peripheral circulation using a photoplethysmographic tail-cuff system and noncontact laser tissue blood flow meter in Wistar rats. Similar to acetylcholine (ACh), ASRE induced dose-dependent relaxation in aortas pre-contracted with phenylephrine; however, in contrast to ACh, ASRE-induced relaxation was partially inhibited by treatments with antagonists of nitric oxide (NO) synthase and soluble guanylyl cyclase as well as by endothelium removal. Contractile responses to phenylephrine or potassium chloride were observed in the presence of ASRE. The oral administration of ASRE (900 mg/kg/d for 1 wk) decreased systolic blood pressure in rats 3 h after the treatment and did not affect heart rate, tail blood flow, mass, or velocity; this decreasing effect was not observed on day 2. A 1-wk treatment with ASRE did not affect vasorelaxation in response to ASRE. These results demonstrate that ASRE induces vasorelaxation via endothelial NO production and an NO-independent pathway in rats. Based on these findings, positive impacts of ASRE on blood pressure and peripheral blood circulation cannot be expected under healthy conditions as the systemic effects of ASRE are temporary. Instead, caution is needed to prevent the occurrence of side effects (i.e., orthostatic dizziness) at the beginning of ASRE dosing.

 
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