Pharmacological characteristics of Artemisia vulgaris L. in isolated porcine basilar artery. (22nd April 2016)
- Record Type:
- Journal Article
- Title:
- Pharmacological characteristics of Artemisia vulgaris L. in isolated porcine basilar artery. (22nd April 2016)
- Main Title:
- Pharmacological characteristics of Artemisia vulgaris L. in isolated porcine basilar artery
- Authors:
- Nguyen, Ha Thi Thanh
Nguyen, Hai Thanh
Islam, Md. Zahorul
Obi, Takeshi
Pothinuch, Pitchaya
Zar, Phyu Phyu Khine
Hou, De Xing
Van Nguyen, Thanh
Nguyen, Tuong Manh
Van Dao, Cuong
Shiraishi, Mitsuya
Miyamoto, Atsushi - Abstract:
- Abstract: Ethnopharmacological relevance: In Vietnamese traditional herbalism, there are conflicting opinions about the effect of Artemisia vulgaris L. (AVL, English name: mugwort) on hypertension. Some ethnic doctors recommend the use of AVL for treatment of hypertension, whereas others advise against it. The purpose of this study was to clarify the pharmacological characteristics of AVL in isolated arteries to explain the conflicts surrounding the use of AVL for treatment of hypertension. Materials and methods: We initially performed a functional study using an organ bath system to investigate the effect of AVL extract on isolated porcine basilar artery. We then measured the change in intracellular free Ca 2+ concentration elicited by AVL using cultured smooth muscle cells loaded with the Ca 2+ indicator fluo-4. Finally, using HPLC, we determined the active components in AVL. Results and discussion: AVL induced vasoconstriction at resting tension, and endothelial removal enhanced this effect significantly. Pretreatment with PD123319 (an AT2 receptor antagonist), Nω - nitro - L - arginine (a nitric oxide synthase inhibitor), or both, also enhanced this effect. AVL-induced contraction was competitively inhibited by methiothepin (a 5-HT1 and 5-HT2 receptor antagonist) in the presence of ketanserin (a 5-HT2 receptor antagonist). Removal of extracellular calcium with nifedipine (an L-type Ca 2+ channel blocker) or ruthenium red (a ryanodine receptor blocker) significantlyAbstract: Ethnopharmacological relevance: In Vietnamese traditional herbalism, there are conflicting opinions about the effect of Artemisia vulgaris L. (AVL, English name: mugwort) on hypertension. Some ethnic doctors recommend the use of AVL for treatment of hypertension, whereas others advise against it. The purpose of this study was to clarify the pharmacological characteristics of AVL in isolated arteries to explain the conflicts surrounding the use of AVL for treatment of hypertension. Materials and methods: We initially performed a functional study using an organ bath system to investigate the effect of AVL extract on isolated porcine basilar artery. We then measured the change in intracellular free Ca 2+ concentration elicited by AVL using cultured smooth muscle cells loaded with the Ca 2+ indicator fluo-4. Finally, using HPLC, we determined the active components in AVL. Results and discussion: AVL induced vasoconstriction at resting tension, and endothelial removal enhanced this effect significantly. Pretreatment with PD123319 (an AT2 receptor antagonist), Nω - nitro - L - arginine (a nitric oxide synthase inhibitor), or both, also enhanced this effect. AVL-induced contraction was competitively inhibited by methiothepin (a 5-HT1 and 5-HT2 receptor antagonist) in the presence of ketanserin (a 5-HT2 receptor antagonist). Removal of extracellular calcium with nifedipine (an L-type Ca 2+ channel blocker) or ruthenium red (a ryanodine receptor blocker) significantly reduced AVL-induced contraction, whereas losartan (an AT1 receptor antagonist) and diphenhydramine (a H1 receptor antagonist) had no effect on this contraction. AVL increased the intracellular free Ca 2+ concentration in cultured cells, and this increment was inhibited by methiothepin. HPLC analysis revealed that the retention time of the first peak in the AVL profile was similar to that of the 5-HT standard, and that addition of 5-HT to the AVL sample enhanced this peak. On the other hand, AVL induced endothelium-independent relaxation under precontracted conditions with 60 mM KCl. Captopril (an angiotensin converting enzyme inhibitor), atenolol (a β1 receptor antagonist) and cimetidine (a H2 receptor antagonist) had no effect on this relaxation. In Ca 2+ -free 60 mM KCl-containing solution, pretreatment with AVL significantly inhibited CaCl2 -induced contraction. Conclusion: For the first time, the present study has demonstrated that AVL has two opposite effects, contraction and relaxation, on isolated artery, which may help to explain the conflicting indications for AVL in traditional herbalism. 5-HT is a significant factor affecting artery contraction in the presence of AVL. Graphical abstract: … (more)
- Is Part Of:
- Journal of ethnopharmacology. Volume 182(2016)
- Journal:
- Journal of ethnopharmacology
- Issue:
- Volume 182(2016)
- Issue Display:
- Volume 182, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 182
- Issue:
- 2016
- Issue Sort Value:
- 2016-0182-2016-0000
- Page Start:
- 16
- Page End:
- 26
- Publication Date:
- 2016-04-22
- Subjects:
- AVL Artemisia vulgaris L. -- CRC concentration response curve -- 2-APB 2-aminoethyl diphenylborinate -- 5-HT 5-hydroxytryptamine -- BK bradykinin -- EGTA ethylene glycol-bis(2-aminoethylether)-N, N, N′, N′-tetraacetic acid -- L-NA Nω-nitro-L-arginine -- SNP sodium nitroprusside -- U46619 9, 11-dideoxy-9α, 11α-methanoepoxy prostaglandin F2α
Serotonin -- Artemisia vulgaris L. -- Mugwort -- Basilar artery -- Biphasic effects -- Hypertension
Ethnopharmacology -- Periodicals
Pharmacognosy -- Periodicals
Herbs -- Periodicals
Herbs -- Periodicals
Pharmacognosy -- Periodicals
Pharmacognosie -- Périodiques
Herbes -- Périodiques
615.1 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03788741 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jep.2016.02.009 ↗
- Languages:
- English
- ISSNs:
- 0378-8741
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4979.602400
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