PP  Vol.10 No.5 , May 2019
Antispasmodic Effects of Salvia officinalis in Isolated Ileum of Rabbit
ABSTRACT
Salvia officinalis has been commonly used in Syria and other Middle East countries in popular medicine for many medical purposes. One of the strong claims about its properties is the spasmolytic effect. The aim of this research was to investigate the spasmolytic effect of ethanolic extract of Salvia officinalis in isolated rabbit ileum preparations. Male rabbits were sacrificed and portions of ileum were isolated and mounted in Tyrode’s solution. Afterwards, the experiments were performed according to different groups with different spasmogenic agents: the first group was only with spontaneous contraction, the second was KCl-induced contractions and the third was Carbachol-induced contractions. The examined extract was added cumulatively in all previous groups. Verapamil was used as a reference. The results showed profound relaxing effect of S. officinalis extract in mentioned groups, especially in the group of KCl-induced contraction. These findings suggest that the main mechanism of the spasmolytic action is related to the inhibition of calcium entry through cell membrane as well as via internal stores.

1. Introduction

Salvia officinalis L. belongs to the family of Lamiaceae. It is a perennial round shrub (Figure 1). This family contains about 1000 species but Salvia is the main genus. The species of S. officinalis grows natively in the Middle East. S. officinalis shrubs, particularly the aerial parts, has a historical record regarding folk medicine.

Figure 1. Salvia officinalis L.

In traditional medicine of Asia and many parts of the world, the plant has widely been used in diverse disorders including: diabetes mellitus [1], bacterial infection [2] tumor and inflammation [3] [4]. Indeed, the effect of this plant was investigated in some nervous system disorders [5] [6]. In food industry, Salvia has been used as flavoring agent in foods [7], as dried leaves or essential oil.

The main important ingredients in essential oil are cineole and borneol. Whereas leaves contain mainly tannic acid, oleic acid, ursonic acid, ursolic acid, niacin, nicotinamide, flavones, flavonoid glycosides, cornsole, cornsolic acid, fumaric acid, chlorogenic acid, caffeic acid, and estrogenic substances [8] [9] [10].

Recently, a lot of researches have been performed to confirm some of the popular uses of S. officinalis or to discover new medicinal properties. Among these biologic effects was Antioxidant, antimicrobial, anticancer, cytotoxic, and hemostatic, as well as many others [11] [12].

Saliva is well known in Syrian traditional medical practice, as many other plants [13], by having several properties [14] [15] [16]. Among these properties it has been claimed that leaves can treat some common digestive problems such as intestinal spasms. However there is no direct scientific evidence to support these claims.

Therefore, by taking into account the traditional uses of S. officinalis, the current work is an approach to explore its rationale on scientific basis. We aim to examine if S. officinalis ethanolic extract has spasmolytic effect on the duodenal smooth muscle as a pharmacological approach to validate its use in traditional medicine. Hence, we designed the current model to elucidate possible mode of action for spasmolytic activity of S. officinalis.

2. Materials and Methods

2.1. Plant Sample Collection and Extraction

The plant was collected from countryside of Damascus in summer 2017 and identified at the faculty of science, Damascus University. The leaves of Salvia officinalis L. were dried in dark and room temperature. The plant extract was prepared by decoction followed by lyophylization. Ground, dried leaves (10 g) were added to 100 ml mixture of 30 ml de-ionized water and 70 ml ethanol and shaken for 24 hours. Solid material was removed by filtration, then the ethanol was evaporated under vacuum and the remaining aqueous extract was lyophilized to dryness. Dried extract was approximately 5% (w/w) of crude material. Working solutions of extract were prepared daily at a concentration of 80 mg/ml in distilled water.

Animals: Locally available breed of male rabbits, weighing between 1.5 and 2 kg, purchased from the Experimental Animal Center of Agriculture research department, Damascus. They were maintained at the animal house of the college of Pharmacy, IUST University, Damascus, Syria at temperature of 25˚C ± 2˚C and exposed to 12 h light-dark cycles were used in experiments. The animals had free access to water and a standard diet. Guide for the care and use of laboratory animals issued by Institute of Laboratory Animal Research, Commission on Life Sciences, NRC was followed.

Chemicals and drugs: The following chemicals and drugs were used: carbachol, verapamil hydrochloride, potassium chloride, and Sodium chloride were purchased from Sigma Chemicals Co. St. Louis, MO. Potassium-di-hydrogen phosphate, glucose, calcium chloride, magnesium sulfate, sodium bicarbonate, sodium-di-hydrogen phosphate and ethanol were purchased from Merck, Darmstadt, Germany. All chemicals used were of the analytical grade and dissolved in distilled water.

Studies on isolated ileum preparations: Rabbits were sacrificed by cervical dislocation, abdomens opened, ileum isolated, cleaned off from the connective tissues and cut into pieces of about 2 cm. Each piece was mounted in a 20 mL organ batch (Harvard Tissue Organ Bath System, England) containing Tyrode’s solution composed of KCl 2.68, NaCl 136.9, MgCl2 1.05, NaHCO3 11.90, NaH2PO4 0.42, CaCl2 1.8, and glucose 5.55 mM, maintained at 37C and continuously bubbled with carbogen (95% O2 and 5% CO2). Spontaneous contractions were recorded under preload of 1 g tension by using force displacement transducer. Isometric tension change was recorded continuously on a two-channel physiological recorder (Dei lierreelectronique, France) connected to a recorder (recorder company, USA). The tissue was allowed to equilibrate for about 30 min with fluid changed at intervals of 10 min before addition of any drug.

2.2. The Study Protocol

Relaxing effect of the extract on spontaneous contraction of ileum:

The tested extract was added on the spontaneous contracting ileum preparations in cumulative doses. Verapamil was used as standard and added cumulatively (10−9 M - 10−5 M). The inhibitory effects of test materials were calculated as percent change in spontaneous contractions of ileum obtained immediately before addition of the test substances.

Relaxant effect of extract on contraction induced by carbachol:

In another set of experiments, the cholinergic agonist, carbachol (1 μM) was used to induce contraction in ileum preparations, and when the plateau was attained (sustained contraction), the extract was added cumulatively to induce a concentration-dependent response [17].

Relaxant effect of extract on contraction induced by KCl (80 mM):

In another set of experiments, K‏ (80 mM), as KCl, was applied on isolated tissue as spasmogenic agent and after achieving sustained contraction, the tested extract was then added to the organ bath in cumulative doses.

The calcium channel blocker, Verapamil, was used as a reference.

Statistical analysis: The relaxant response to the extract was expressed as a percentage of the extract-induced contraction. IC50 values were obtained as the extract concentration causing a half-maximum relaxation and were calculated by non-linear regression analysis of the concentration-response curves using all the data point. Results are expressed as the Means ± S.E.Ms for n separate experiments. Data were analyzed by Student t-test and a probability of less than 0.05 was regarded significant.

3. Results

Effect of the extract on spontaneous contraction of ileum:

Salvia officinalis L. extract produced concentration-dependent inhibition of spontaneous contraction exhibited by ileum preparations comparing with the control group, P < 0.05 (IC50 = 6320 mg/L), the effect was dose-dependent (Table 1, Figure 2 and Figure 4). Verapamil induced relaxation in a dose-dependent manner (Figure 3 and Figure 4).

Effect of the extract on carbachol-induced contraction:

S. officinalis L. extract produced concentration-dependent inhibition on contraction induced by carbachol of ileum preparations comparing with the control group, P < 0.05 (IC50 = 4870 mg/L), the effect was dose-dependent (Figure 5 and Figure 6).

Table 1. The inhibitory effect of Salvia officinalis L. extract on spontaneous contraction of rabbit ileum.

Figure 2. The effect of Salvia officinalis L. extract on spontaneous contraction of rabbit ileum.

Figure 3. The effect of verapamil on spontaneous contraction of rabbit ileum.

Figure 4. The trace of effects of S. officinalis L. extract (A), and Verapamil (B) on ileum spontaneous contraction.

Figure 5. The effect of S. officinalis L. extract on carbacol-induced contraction of ileum.

Figure 6. The trace of S. officinalis L. extract’s effect on carbacol-induced contraction of ileum.

Effect of extract on contraction induced by KCl (80 mM):

The extract induced concentration-dependent inhibition on contraction induced by KCl of ileum preparations comparing with the control group, P < 0.05 (IC50 = 5640 mg/L), the effect was dose-dependent (Figure 7 and Figure 9).

Verapamil induced relaxation in a dose-dependent manner (Figure 8 and Figure 9).

4. Discussion

The aim of our study is to detect the relaxant effect of S. officinalis L. extract on the smooth muscle of ileum. The use of this plant in traditional medicine as spasmolytic and the lack of scientific evidence have made this study necessary. Our results showed clearly that the extract relaxed spontaneous, carbacol-induced and KCl-induced contractions.

The spontaneous contraction is regulated by depolarization and repolarization induced by Ca+2 movement into cytoplasm via voltage-dependent calcium channels and through releasing from internal stores [18] [19] [20], whereas relaxation is induced by removal of calcium from cytoplasm. In this study, the extract showed the ability, in a dose-dependent manner, to reduce spontaneous

Figure 7. Effect of S. officinalis L. extract on KCl-induced contraction of ileum.

Figure 8. The effect of Verapamil on KCl-induced contraction of ileum.

Figure 9. (A) The trace of S. officinalis L. extract’s effect on KCl-induced contraction of ileum; (B) The trace of Verapamil’s effect on KCl-induced contraction of ileum.

contraction. This relaxing action may be due by influencing the entry or releasing of calcium into the cytoplasm. In this regard, the extract was similar to Verapamil, the calcium channel blocker, in inhibiting spontaneous contraction.

The study of extract effect on spontaneous contraction is an important procedure and many researchers perform this essential procedure when studying the effect of their extracts on ileum contraction. The most acceptable explanation for inhibitory effect on spontaneous contraction on ileum is the interaction of extract with calcium entry via smooth muscle membrane [21] [22].

As a step toward clarifying and further investigating the relaxing effect of extract, we studied the effect on contraction induced by high concentration of KCl (80 mM). This is an important step to clarify the mechanism of relaxing effect, because this kind of contraction is induced via entering of Ca+2 through calcium channels [22] [23].

The findings showed that the extract completely inhibited KCl-induced contraction, and was similar to the effect of Verapamil, the calcium channel blocker. This effect means that the extract has an ability to block calcium entry through calcium channels, as calcium channel blockers do. This explanation is the most agreeable among researchers [24], like Sadraei who indicated clearly that his investigated extract had profound blocking effect on calcium entry via membrane channels, which he considered the basic mechanism beyond the relaxing effect of his tested plant [25].

The extract inhibited the contraction induced by the cholinergic agonist, carbachol. As in case of KCl-induced contraction, the inhibitory effect was dose-dependent but the extract did not completely abolish the contraction.

Cholinergic agonists, contract the smooth muscle of ileum through stimulating M3 receptors [26] [27] ; which in turn activate second messengers like inositol trisphosphate (IP3) and diacylglycerol and these intracellular mediators are responsible for releasing calcium ions (Ca+2) from internal stores [28] [29]. Since our extract could inhibit the contraction induced by activating M3, this may mean it has the ability to block these receptors or poses ingredients that can affect the intracellular signals and mediators which are activated via M3 receptors stimulation [30] [31].

5. Conclusion

S. officinalis L. extract has profound relaxing effect for normal, KCl and carbachol-induced contraction. This effect, as the results show, is related mostly to suppress calcium movement via both cell membrane and internal stores. We strongly recommend further investigation on isolated active compounds to clarify their role in the mechanism of relaxing action.

NOTES

*The authors contribute equally to this paper.

Cite this paper
Al-Aghawani, W. and Naser, I. (2019) Antispasmodic Effects of Salvia officinalis in Isolated Ileum of Rabbit. Pharmacology & Pharmacy, 10, 223-233. doi: 10.4236/pp.2019.105019.
References
[1]   Belhadj, S., Hentati, O., Hammami, M., Ben Hadj, A., Boudawara, T., Dammak, M., Zouari, S. and El Feki, A. (2018) Metabolic Impairments and Tissue Disorders in Alloxan-Induced Diabetic Rats Are Alleviated by Salvia officinalis L. Essential Oil. Biomedicine & Pharmacotherapy, 108, 985-995.
https://doi.org/10.1016/j.biopha.2018.09.108

[2]   Pavic, V., Jakovljevic, M., Molnar, M. and Jokic, S. (2019) Extraction of Carnosic Acid and Carnosol from Sage (Salvia officinalis L.) Leaves by Supercritical Fluid Extraction and Their Antioxidant and Antibacterial Activity. Plants (Basel), 8, E16.
https://doi.org/10.3390/plants8010016

[3]   Garcia, C.S., Menti, C., Lambert, A.P. and Barcellos, T. (2016) Pharmacological Perspectives from Brazilian Salvia officinalis (Lamiaceae): Antioxidant, and Antitumor in Mammalian Cells. The Anais da Academia Brasileira de Ciências, 88, 281-292.
https://doi.org/10.1590/0001-3765201520150344

[4]   Rodrigues, M.R., Kanazawa, L.K., das Neves, T.L. and da Silva, C.F. (2012) Antinociceptive and Anti-Inflammatory Potential of Extract and Isolated Compounds from the Leaves of Salvia officinalis in Mice. Journal of Ethnopharmacology, 139, 519-526.
https://doi.org/10.1016/j.jep.2011.11.042

[5]   Moss, M., Smith, E., Milner, M. and McCready, J. (2018) Acute Ingestion of Rosemary Water: Evidence of Cognitive and Cerebrovascular Effects in Healthy Adults. Journal of Psychopharmacology, 32, 1319-1329.
https://doi.org/10.1177/0269881118798339

[6]   Perry, N.S.L., Menzies, R., Hodgson, F. and Wedgewood, P. (2018) A Randomised Double-Blind Placebo-Controlled Pilot Trial of a Combined Extract of Sage, Rosemary and Melissa, Traditional Herbal Medicines, on the Enhancement of Memory in Normal Healthy Subjects, Including Influence of Age. Phytomedicine, 39, 42-48.
https://doi.org/10.1016/j.phymed.2017.08.015

[7]   Walch, S.G., Kuballa, T., Stuhlinger, W. and Lachenmeier, D.W. (2011) Determination of the Biologically Active Flavour Substances Thujone and Camphor in Foods and Medicines Containing Sage (Salvia officinalis L.). Chemistry Central Journal, 5, 1-10.
https://doi.org/10.1186/1752-153X-5-44

[8]   Abu-Darwish, M.S., Cabral, C., Ferreira, V. and Gonçalves, M.J. (2013) Essential Oil of Common Sage (Salvia officinalis L.) from Jordan: Assessment of Safety in Mammalian Cells and Its Antifungal and Anti-Inflammatory Potential. BioMed Research International, 2013, Article ID: 538940.
https://doi.org/10.1155/2013/538940

[9]   Khedher, M.R.B., Khedher, S.B., Chaieb, I., Tounsi, S. and Hammami, M. (2018) Chemical Composition and Biological Activities of Salvia officinalis Essential Oil from Tunisia. Experimental and Therapeutic Medicine, 15, 1863-1870.

[10]   Cocan, I., Alexa, E., Danciu, C. and Radulov, I. (2018) Phytochemical Screening and Biological Activity of Lamiaceae Family Plant Extracts. Experimental and Therapeutic Medicine, 15, 1863-1870.

[11]   Tayarani-Najarana, Z., Mousavi, S.H., Tajfarda, F., Asilid, J. and Soltanie, S. (2013) Cytotoxic and Apoptogenic Properties of Three Isolatedditerpenoids from Salvia chorassanica through Bioassay-Guided Fractionation. Food and Chemical Toxicology, 57, 346-351.
https://doi.org/10.1016/j.fct.2013.03.037

[12]   Jiang, Y., Zhang, L. and Rupasinghe, H.P. (2017) Antiproliferative Effects of Extracts from Salvia officinalis L. and Saliva miltiorrhiza Bunge on Hepatocellular Carcinoma Cells. Biomedicine & Pharmacotherapy, 85, 57-67.
https://doi.org/10.1016/j.biopha.2016.11.113

[13]   Alaghawani, W. and Naser, I. (2013) Study the Hypoglycemic Effect of Crataegus laevigata in Diabetic Rats. International Journal of Pharmaceutical and Clinical Research, 5, 145-149.

[14]   El Astal, Z.Y., Ashour, E.-R.A. and Kerrit, A.A.-M. (2005) Antimicrobial Activity of Some Medicinal Plant Extracts in Palestine. Pakistan Journal of Medical Sciences, 21, 187-193.

[15]   Amr, S. and Dordevi’c, S. (2000) The Investigation of the Quality of Sage (Salvia officinalis L.). Originating from Jordan, 1, 103-108.

[16]   Al-Qura’n, S. (2008) Taxonomical and Pharmacological Survey of Therapeutic Plants in Jordan. Journal of Natural Products, 1, 10-26.

[17]   Aslam, N. and Janbaz, K.H. (2017) Antispasmodic and Bronchorelaxant Activities of Salsola imbricata Are Mediated through Dual Ca+2 Antagonistic and β-Adrenergic Agonistic Effects. Pharmaceutical Biology, 55, 1131-1137.
https://doi.org/10.1080/13880209.2017.1291691

[18]   Montgomery, L.E., Tansey, E.A., Johnson, C.D., Roe, S.M. and Quinn, J.G. (2016) Autonomic Modification of Intestinal Smooth Muscle Contractility. Advances in Physiology Education, 40, 104-109.
https://doi.org/10.1152/advan.00038.2015

[19]   Voussen, B., Beck, K., Mauro, N., Keppler, J. and Friebe, A. (2018) Comparison of Nitrergic Signaling in Circular and Longitudinal Smooth Muscle of Murine Ileum. Neurogastroenterology & Motility, 30, e13175.
https://doi.org/10.1111/nmo.13175

[20]   Grasa, L., Rebollar, E., Arruebo, M.P., et al. (2004) The Role of Ca2+ in the Contractility of Rabbit Small Intestine in Vitro. Journal of Physiology and Pharmacology, 55, 639-650.

[21]   Khan, A.U., Ali, S., Gilani, A.H., Ahmed, M. and Choudhary, M.I. (2017) Antispasmodic, Bronchodilator, Vasorelaxant and Cardiosuppressant Effects of Buxus papillosa. BMC Complementary and Alternative Medicine, 17, 54.
https://doi.org/10.1186/s12906-017-1558-x

[22]   Khan, H., Ali, I., Khan, A.U., Naz, R. and Gilani, A.H. (2012) Antibacterial, Antifungal, Antispasmodic and Ca2+ Antagonist Activities of Caesalpinia bonducella. Natural Product Research, 25, 444-449.
https://doi.org/10.1080/14786419.2010.529445

[23]   Ali, N., Jamil, A., Shah, S.W., Shah, I. and Ahmed, G. (2017) Spasmogenic and Spasmolytic Activity of Rind of Punica granatum Linn. BMC Complementary and Alternative Medicine, 17, 97.
https://doi.org/10.1186/s12906-017-1616-4

[24]   Sadraei, H., Asghari, G. and Alipour, M. (2016) Anti-Spasmodic Assessment of Hydroalcoholic Extract and Essential Oil of Aerial Part of Pycnocycla caespitosa Boiss. & Hausskn on Rat Ileum Contractions. Research in Pharmaceutical Sciences, 11, 33-42.

[25]   Sadraei, H., Asghari, G. and Alinejad, M. (2016) Comparison of Antispasmodic Effect of Hydroalcoholic Extract of Dracocephalum kotschyi Boiss. in Rat Uterus and Ileum. Research in Pharmaceutical Sciences, 11, 284-292.
https://doi.org/10.4103/1735-5362.189295

[26]   Eglen, R.M., Hegde, S.S. and Watson, N. (1996) Muscarinic Receptor Subtypes and Smooth Muscle Function. Pharmacological Reviews, 48, 531-565.

[27]   Sadraei, H., Asghari, G. and Jalali, F. (2016) Assessment of Hydroalcoholic and Hexane Extracts of Rosa persica Mich. Flower on Rat Ileum Spasm. Research in Pharmaceutical Sciences, 11, 160-167.
https://doi.org/10.4103/1735-5362.189295

[28]   More, J.L., Macrez, N. and Mironneau, J. (1997) Specific Gq Protein Involvement in Muscarinic M3 Receptor-Induced Phosphatidylinositol Hydrolysis and Ca2+ Release in Mouse Duodenal Myocytes. British Journal of Pharmacology, 121, 451-458.
https://doi.org/10.1038/sj.bjp.0701157

[29]   Ritter, J., et al. (2012) Rang & Dale’s Pharmacology. 7th Edition, Elsevier, Amsterdam, 151-157.
https://doi.org/10.1016/B978-0-7020-3471-8.00013-5

[30]   Sadraei, H., Asghari, G. and Farahnaki, F. (2015) Assessment of Hydroalcoholic Extract of Seeds and Leaves of Moringa peregrina on Ileum Spasm. Research in Pharmaceutical Sciences, 10, 252-258.

[31]   Saikia, B., Barua, C.C., Haloi, P. and Patowary, P. (2017) Anticholinergic, Antihistaminic, and Antiserotonergic Activity of n-Hexane Extract of Zanthoxylum alatum Seeds on Isolated Tissue Preparations: An ex Vivo Study. Indian Journal of Pharmacology, 49, 42-48.

 
 
Top