Pharmacognosy Magazine

ORIGINAL ARTICLE
Year
: 2010  |  Volume : 6  |  Issue : 24  |  Page : 282--285

Effects of Achillea wilhelmsii on rat's gastric acid output at basal, vagotomized, and vagal-stimulated conditions


S Niazmand1, E Khooshnood2, M Derakhshan3,  
1 Department of Physiology, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran
2 Department of Biology, Sciences School, Azad University of Mashhad, Mashhad, Iran
3 Department of Clinical Microbiology and Virology in Ghaem Hospital and Buali Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran

Correspondence Address:
S Niazmand
Department of Physiology, Medical school, Mashhad University of Medical Sciences (MUMS), Mashhad
Iran

Abstract

Background: Achillea is a plant widely used in traditional medicine for gastrointestinal disorders. There are some reports on gastrointestinal effects of Achillea, such as antiulcer, antibacterial, hepatoprotective, choleretic, and antispasmodic. To investigate the effects of aqueous-ethanol extract of Achillea wilhelmsii on rat«SQ»s gastric acid output in basal, vagotomized (VX), and vagal-stimulated conditions. Materials and Methods: 24 male Wistar rats were randomly divided into 2 groups: control and test. Gastroduodenostomy was performed for each rat. Gastric content was collected for 30 min by washout technique. One milliliter of 3 doses (0.5, 1, and 2 mg/kg) was introduced into the stomach of each rat in the test group and the same volume of saline was used in the control group. Total titratable acid was measured by a titrator. Results: The extract inhibited acid output significantly in basal condition by 1 and 2 mg/kg doses (P < 0.05) but in VX condition this inhibitory effect on acid output disappeared and the 1 and 2 mg/kg doses increased acid output significantly (P < 0.05 and P < 0.001, respectively). The extract showed a reduction in the acid output in vagal-stimulated condition by 1 and 2 mg/kg doses, which were not statistically significant. Conclusion: These results showed an inhibitory effect of A. wilhelmsii extract on acid output in basal condition. The inhibitory effect of the extract was exerted via gastric vagal parasympathetic nerve.



How to cite this article:
Niazmand S, Khooshnood E, Derakhshan M. Effects of Achillea wilhelmsii on rat's gastric acid output at basal, vagotomized, and vagal-stimulated conditions.Phcog Mag 2010;6:282-285


How to cite this URL:
Niazmand S, Khooshnood E, Derakhshan M. Effects of Achillea wilhelmsii on rat's gastric acid output at basal, vagotomized, and vagal-stimulated conditions. Phcog Mag [serial online] 2010 [cited 2019 Oct 23 ];6:282-285
Available from: http://www.phcog.com/text.asp?2010/6/24/282/71791


Full Text

 Introduction



Gastrointestinal disorders due to abnormal metabolic or physical processes, such as gastric and duodenal ulcers, gastritis, dyspepsia, hyperchlorhydria, or functional gastrointestinal disorders, such as irritable bowel syndrome (IBS), are highly prevalent worldwide. [1] Several metabolic and physical disorders related to gastric acid and gastric motility disturbances have been treated by using synthetic and herbal medicines. Medicinal plants have been used for over 2000 years and an increasing attention has been paid to herbal medicine products because of their effectiveness and lower cost in recent years. Achillea is one of the most important genera of the Compositae family and comprises more than 120 spices. Several effects, such as anti-inflammatory, [2] antibacterial, [3],[4] antihypertensive, and anti-hyperlipidemia, [5] and antitumor, [6],[7] have been reported for Achillea. It is widely used in traditional medicine for gastrointestinal disorders [8] and there are some reports of its effects, such as antispasmodic, [9],[10] choleretic, [11] antiulcer, [12] antibacterial (Helicobacter pylori), [13] and hepatoprotective, on the gastrointestinal tract. [10] Achillea wilhelmsii is the major spice, which is grown in Iran and widely used in Iranian traditional medicine for gastrointestinal disorders. It has chemical components, including flavonoids, alkaloids (achilleine), cineol, borneol, α- and β-pinen, camphor, caryophyllene, thujene, rutin, sesquiterpenoids, and monoterpenoids.[14],[15],[16],[17] No reports on its effect on gastric acid output are available at the moment. Thus, the aim of this study was to investigate possible effects of aqueous-ethanol extract of A. wilhelmsii on gastric acid output. To further clarify the interaction of the extract with gastric vagal parasympathetic system, we considered 3 conditions: basal, vagotomized, and vagal stimulated.

 Materials and Methods



Plant material

The aerial part of A. wilhelsii was collected from South Khorasan Province, Iran, and identified by botanists in the Herbarium of Pharmacy School, Mashhad University of Medical Sciences (voucher No. 142-2012-4) and then dried at room temperature.

Extraction method

Three hundred grams of aerial parts of the plant were soaked in ethanol (50%) for 24 h and paper filter was used to filter the solute after mixing. The solution was then dried using a 40°C oven for 36 h. The dried extract was dissolved in the distilled water to make 0.5, 1, and 2 mg/kg doses.

Experimental procedure

The experiment was conducted using 24 male Wistar rats (weighed 200-250 g). The animals were kept in a 20°C±2°C temperature with a 12 h light/dark cycle and fed with standard diet and tap drinking water. The study was permitted by the Institutional Animal Ethics Committee of Mashhad University of Medical Sciences (MUMS). Animals were randomly divided into 2 groups: control and test. The surgical procedure was performed for all the groups. In the test group, the extract was administered and in the control group, saline was used instead of the extract. All the rats were not fed for 24 h but were allowed access to drinking water before operation. To avoid the effect of circadian rhythm, the experiments were started at 8:00 AM every day. Anesthesia was induced by sodium thiopental (50 mg/kg; ip) and cervical esophagus was ligated after tracheostomy. A midline incision was performed on abdomen and a silicone tube (2.5 mm in external diameter) was introduced to the stomach via duodenum. [18] For emptying the remaining gastric contents, the stomach was washed with 1 mL of 37°C normal saline (pH = 7). In VX condition, vagus nerve in the cervical region was dissected and the extract was introduced to the stomach. In vagal-stimulated condition, the vagus nerve was stimulated (15 V, 4 Hz, width 0.05 ms, 30 min) by a stimulator (Harvard Apparatus, England). [19] Gastric acid output was measured 30 min after the extract was introduced to the stomach and the acid output was calculated and reported as mEq/30 min. The gastric content was titrated by NaOH (0.01 N). To measure the gastric acid output in the test group, 1 mL of 0.5, 1, and 2 mg/kg of the aqueous-ethanol extract was introduced into the stomach of each rat for 30 min.

Data analysis

The data were represented as mean ± SEM and analyzed by Wilcoxon signed rank test. P < 0.05 was considered significant.

 Results



Basal acid output in the test group showed a significant decrease with 1 and 2 mg/kg doses of the extract in comparison to the control group (45.2% and 43.2%, respectively, P < 0.05) [Figure 1]. In VX condition, the test group showed a rise in the acid output, which was significant by the 1 and 2 mg/kg doses in comparison to the control group (45% and 129%, P < 0.05 and P <0.001, respectively) [Figure 2]. In vagal stimulation condition, the extract showed a reduction in the acid output by 1 and 2 mg/kg doses (10% and 7%, respectively), which were not statistically significant in comparison to the control group [Figure 3]. {Figure 1}{Figure 2}{Figure 3}

 Discussion



Recent studies have revealed some effects of Achillea on gastrointestinal tract as mentioned in the Introduction, but previous studies have not precisely clarified the probable mechanism involved in gastric acid output. The results of this study indicate that the aqueous-ethanol extract of A. wilhelmsii had an inhibitory effect on gastric acid output in basal condition. This inhibitory effect disappeared at VX condition and prominent excitatory effects were shown; thus the inhibitory effect of the extract in basal condition should be exerted via gastric vagal parasympathetic nerve. The doses of 1 and 2 mg/kg showed inhibitory effect on gastric acid output in basal condition, but at VX condition they had excitatory effect on gastric acid output in comparison with the control group. This may indicate the presence of compound/s with an excitatory effect on gastric acid secretion in the extract that act through processes other than gastric parasympathetic system. The inhibitory effect of the extract on gastric acid output in vagal-stimulated condition was not significant, thus it may be concluded that the extract was unable to overcome the excitatory effect of the vagal stimulation on gastric acid secretion. The previous studies showed that Achillea reduced the gastric acidity and increase the mucus synthesis and excretory function of the stomach. [20],[21] The antiulcer and gastroprotective effect of Achillea may be partly due to the reductive potential of gastric acid output at basal condition. There is another study that shows cineole, one of the main constituent of A. wilhelmsii, has inhibitory effect on gastric acid secretion that leads to its gastroprotective effect. [22]

 Conclusion



Our findings show that the A. wilhelmsii extract has an inhibitory effect on gastric acid output in basal condition via the gastric parasympathetic nerve. But the extract has no effect in vagal-stimulated condition.

 Acknowledgments



This work was supported by the vice chancellor for research in Mashhad University of Medical Sciences (MUMS) [No: 186334]. The authors thank Dr SA Rezaee for his critical reading of the manuscript and valuable advice.

References

1Del Valle J. peptic ulcer disease and related disorders. In: Dennis LK, editor. Harrison's principles of internal medicine. 16 th ed. New York: McGraw- Hill Medical Publishing Division; 2005. p. 1746-62.
2Benedek B, Kopp B, Melzig MF. Achillea millefolium L. s.l. is the anti-inflammatory activity mediated by protease inhibition? J Ethnopharmacol. 2007;113:312-7.
3Candan F, Unlu M, Tepe B, Daferera D, Polissiou M, Sokmen A, et al. Antioxidant and antimicrobial activity of the essential oil and methanol extracts of Achillea millefolium subsp. millefolium Afan. (Asteraceae). J Ethnopharmacol 2003;87:215-20.
4Stojanovic G, Radulovic N, Hashimoto T, Palic R. In vitro antimicrobial activity of extracts of four Achillea species: the composition of Achillea clavennae L. (Asteraceae) extract. J Ethnopharmacol 2005;101:185-90.
5Asgary S, Naderi GH, Sarrafzadegan N, Mohammadifard N, Mostafavi S, Vakili R. Antihypertensive and antihyperlipidemic effects of Achillea wilhelmsii. Drugs Exp Clin Res 2000;26:89-93.
6Tozyo T, Yoshimura Y, Sakurai K, Uchida N, Takeda Y, Nakai H, et al. Antitumor sesquiterpenoids in Achillea millefolium. Chem Pharm Bull (Tokyo) 1994;42:1096-100.
7Csupor-Lِffler B, Hajdْ Z, Zupkَ I, Rιthy B, Falkay G, Forgo P, et al. Antiproliferative effect of flavonoids and sesquiterpenoids from Achillea millefolium s.l. on cultured human tumour cell lines. Phytother Res 2009;23:672-6.
8Nemeth E, Bernath J. Biological activities of yarrow species (Achillea spp.). Curr Pharm Des 2008;14:3151-67.
9Lemmens-Gruber R, Marchart E, Rawnduzi P, Engel N, Benedek B, Kopp B. Investigation of the spasmolytic activity of the flavonoid fraction of Achillea millefolium s.l. on isolated guinea-pig ilea. Arzneimittelforschung 2006;56:582-8.
10Yaeesh S, Jamal Q, Khan AU, Gilani AH. Studies on hepatoprotective, antispasmodic and calcium antagonist activities of the aqueous-methanol extract of Achillea millefolium. Phytother Res 2006;20:546-51.
11Benedek B, Geisz N, Jδger W, Thalhammer T, Kopp B. Choleretic effects of yarrow (Achillea millefolium s.l.) in the isolated perfused rat liver. Phytomedicine 2006;13:702-6.
12Cavalcanti AM, Baggio CH, Freitas CS, Rieck L, de Sousa RS, Da Silva-Santos JE, et al. Safety and antiulcer efficacy studies of Achillea millefolium L. after chronic treatment in Wistar rats. J Ethnopharmacol 2006;107:277-84.
13Mahady GB, Pendland SL, Stoia A, Hamill FA, Fabricant D, Dietz BM, et al. In vitro susceptibility of Helicobacter pylori to botanical extracts used traditionally for the treatment of gastrointestinal disorders. Phytother Res 2005;19:988-91.
14Dokhani S, Cottrell T, Khajeddin J, Mazza G. Analysis of aroma and phenolic components of selected Achillea species. Plant Foods Hum Nutr 2005;60:55-62.
15Afsharypuor S, Asgary S, Lockwood GB. Constituents of the essential oil of Achillea wilhelmsii from Iran. Planta Med 1996;62:77-8.
16Gherase F, Spac A, Dorneanu V, Stγnescu U, Grigorescu E. Pharmacognostic research of some species of Achillea . Note 1. Volatile oils analysis. Rev Med Chir Soc Med Nat Iasi. 2003;107:188-91.
17Javidian K, Miri R, Sadeghpour H. Composition of the volatile oil of Achillea wilhelmsii C. Koch from Iran. Daru 2004;12:63-6.
18Stephens RL, Ishikawa T, Weiner H, Norin D, Tache Y. TRH analogue, RX 77368, injected into dorsal vagal complex stimulated gastric acid secretion. Am J Physiol 1988;245:G639-43.
19Salim AS. Gastric diversion, a method for H+ output estimation in the rat. Digestion 1988;39:47-51.
20Vymiatnina ZK, Gridneva VI. Effect of Achillea asiatica Serg. on gastric secretory and excretory activity. Eksp Klin Farmakol 1997;60:54-7.
21Stojanovic G. Experimental study of the effect of the phytomixture made of leaves of Plantago major L. and Achillea millenfolium L. on the secretion activity of the stomach in dogs. Eksp Klin Gastroenterol 2005;4:73-6, 113.
22Santos FA, Rao VS. 1, 8-cineol, a food flavoring agent, prevents ethanol-induced gastric injury in rats. Dig Dis Sci 2001;46:331-7.