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| Year : 2015 | Volume
: 47
| Issue : 1 | Page : 109-113 |
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Interaction of aqueous leaf extract of Aegle marmelos (L.) Corr. with cholinergic, serotonergic and adrenergic receptors: An ex vivo study
Sanjeev Kumar, Rakesh Kumar Mahaseth, Mukesh Tiwari, Ratika Sehgal, Preety Rajora, Rajani Mathur
Department of Pharmacology, Delhi Institute of Pharmaceutical Sciences and Research, Pushp Vihar, New Delhi, India
| Date of Submission | 01-Aug-2014 |
| Date of Decision | 16-Oct-2014 |
| Date of Acceptance | 27-Nov-2014 |
| Date of Web Publication | 30-Jan-2015 |
Correspondence Address:
Dr. Rajani Mathur
Department of Pharmacology, Delhi Institute of Pharmaceutical Sciences and Research, Pushp Vihar, New Delhi
India
 Source of Support: Government. of N.C.T. of Delhi., Conflict of Interest: None  | Check |
DOI: 10.4103/0253-7613.150374
Objectives: The aim was to study interaction of aqueous leaf extract of Aegle marmelos (AM) with cholinergic, serotonergic, and adrenergic receptor systems using appropriate rat tissues-ileum, fundus and tracheal chain, respectively.
Materials and Methods: Cumulative concentration-response curves (CRC) were constructed at various doses on each tissue for AM and respective standard agonist. The CRC was again plotted in presence and absence of respective standard antagonist to confirm the interaction of receptor system and AM.
Results: AM induced concentration-dependent contractions in isolated rat ileum (0.2-6.4 mg/ml) and fundus (0.2-3.2 mg/ml) that were inhibited significantly (P < 0.05) in the presence of atropine (10−7 M) and ketanserin (10−6 M), respectively. The relaxant effect, produced by AM (0.2 mg/ml) on carbachol (10−5 M) precontracted rat tracheal chain, was also inhibited significantly (P < 0.05) by propranolol (1 ng/ml).
Conclusion: It may be concluded that AM possesses agonistic activity on cholinergic, serotonergic and adrenergic receptors.
Keywords: Aegle marmelos, fundus, ileum, single channel organ bath, tracheal chain
How to cite this article:
Kumar S, Mahaseth RK, Tiwari M, Sehgal R, Rajora P, Mathur R. Interaction of aqueous leaf extract of Aegle marmelos (L.) Corr. with cholinergic, serotonergic and adrenergic receptors: An ex vivo study. Indian J Pharmacol 2015;47:109-13 |
How to cite this URL:
Kumar S, Mahaseth RK, Tiwari M, Sehgal R, Rajora P, Mathur R. Interaction of aqueous leaf extract of Aegle marmelos (L.) Corr. with cholinergic, serotonergic and adrenergic receptors: An ex vivo study. Indian J Pharmacol [serial online] 2015 [cited 2023 Jun 5];47:109-13. Available from: https://www.ijp-online.com/text.asp?2015/47/1/109/150374 |
| » Introduction | |  |
The use of plants as a source of herbal medicine has been an innate and vital aspect of India's healthcare system. Like allopathic drugs, herbal medicines also have different pharmacokinetic and pharmacodynamic properties, which ultimately lead to therapeutic responses, but sometimes cause adverse actions and/or drug-herbal interactions. Understanding the interaction of herbal medicine with various receptor systems can provide the basis for their rational therapeutic use. Many adverse effects of drugs and drug toxicities can be anticipated by understanding the mechanism(s) of action of the drug, its pharmacokinetics, and its interactions with various receptor systems. [1]
Aegle marmelos (AM) (L.) Corr., (Rutaceae) is commonly known as bael/bilva, which is considered as a sacred tree by the hindus. The bael tree has great mythological significance, and the leaves of the tree are traditionally used as sacred offerings to Lord Shiva. Various pharmacological properties of AM such as hypoglycemic, hypolipidemic, antioxidant, analgesic, antiinflammatory, hepato-protective have been known for a long time, and these have been corroborated in pharmacological studies. [2],[3],[4],[5],[6],[7]
Despite wide variety of therapeutic use in the traditional system of medicine and their validation in pharmacological studies, no information about its interaction with receptor system is available. Due to the presence of multiple active constituents in medicinal plants, receptor binding studies are not suitable for evaluating their interactions with receptor systems. The objective of this study was to carry out preliminary investigation using ex vivo preparations to study the interaction of aqueous leaf extract of AM (L.) Corr. with cholinergic, serotonergic and adrenergic receptor systems.
| » Materials and Methods | | |
Drugs and Reagents
The drugs used were 5-hydroxytryptamine and ketanserin (+) tatrate (Sigma Eldrich, India), acetycholine hydrochloride and atropine sulphate (Himedia, India), isoprenaline and propranolol HCl (Samarth Pharma, India) and carbachol (CCh) (TCI Chemicals, India). Other chemicals, including the reagents used in the preparation of physiological solutions were of analytical grade.
Plant Material and Preparation of Extract
Fresh leaves of the plant were collected, identified (NHCP/NBPGR/2009-21), weighed, washed, dried in the shade and powdered. The powder was mixed with distilled water (1:10 w/v) and stirred at room temperature for 2 h. The extract was then filtered, frozen at −20°C and lyophilized at −70°C under vacuum. Percentage yield of powder with respect to dry powder was 16.33% w/w. Preliminary phytochemical screening was done as per standard procedures.
Animals
Male Wistar albino rats weighing 150-250 g were selected for the study and housed in standard environmental conditions (temperature 25°C ± 2°C and 12 h dark and light cycle) and fed with rodent pellet diet and drinking water ad libitum. The study was approved by Institutional Animal Ethical Committee (IAEC/2013/18).
Tissue Preparation
Overnight fasted rats with free access to water were euthanized under CO 2 and dissected. After isolation, ileum was placed in Tyrode's solution, whereas trachea and fundus were placed in Kreb's solution. Tissue preparation was performed as per the method described below and responses of the tissues were recorded using single channel organ bath (50 mL) (Radnoti Single Channel Organ Bath, USA) and data was acquired using polyVIEW 16 (version 1.1) Data Acquisition System (Grass Technologies, USA).
Ileum
Ileum was cleaned off from extraneous tissue and lumen was cleaned with gentle care by flushing the Tyrode's solution into it. Ileum (1 cm) was mounted in the organ bath maintained at 37°C and constantly bubbled with carbogen and allowed to equilibrate for 30 min. Subsequently, concentration response curves (CRC) of acetylcholine (Ach) (10−9 -10−4 M) alone, ACh in the presence of atropine (10−7 M), AM (0.2, 0.4, 0.8, 1.6 and 3.2 mg/ml) alone and AM in presence of atropine (10−7 M) were recorded.
Fundus
The fundus portion of the stomach was cut and opened along the lesser curvature into a sheet, and a 1 cm long strip was prepared by cutting along the longitudinal fibers. The strip was mounted and allowed to equilibrate in Kreb's solution maintained at 37°C and constantly bubbled with carbogen for 45 min in the organ bath. Subsequently, CRC of 5-HT (10−9 -10−5 M) alone, 5-HT in the presence of ketanserin (10−6 M), AM (0.2, 0.4, 0.8, 1.6 and 3.2 mg/ml) alone and AM in presence of ketanserin (10−6 M) were recorded.
Tracheal Chain
The tracheal tissue was cleaned of extraneous tissue and cut into 5-6 rings, each containing 2-3 cartilaginous rings. These rings were connected in series by means of short loops of silk thread to form a tracheal chain according to the method described in Kulkarni. [8] The tracheal chain was mounted in organ bath and was allowed to equilibrate in Kreb's solution maintained at 37°C and constantly bubbled with carbogen for 45 min and a CRC was obtained with CCh (10−9 -10−4 M) to identify the sub-maximal concentration. The response of isoprenaline (10−6 M) on CCh (10−5 M, as identified) precontracted tracheal chain alone and also in the presence of propranolol (1 ng/ml) was recorded. Further response of AM (0.2 mg/ml) on CCh (10−5 M) contracted tracheal chain alone and also in the presence of propranolol (1 ng/ml) was recorded.
Doses were selected by titrating various concentrations of AM starting from 1 μg/mL and increasing by ×10 in each step.
Statistical Analysis
All the data were expressed as mean ± SEM (n = 3). Student t-test was used to compare the two groups. Significance was accepted at P < 0.05.
| » Results | | |
AM tested positive for the presence of alkaloids, cardiac glycosides, terpenoids, reducing sugars, saponins, tannins, steroids, flavonoids, and proteins.
In isolated rat ileum, ACh as well as AM induced concentration-dependent contractions. In the presence of atropine (10−7 M), a rightward shift in the CRC of ACh [[Figure 1]a] as well as AM [[Figure 1]b] was recorded. The EC 50 of ACh in presence of atropine (4.56 ± 0.73 × 10−8 M) was significantly higher (P < 0.05) than EC 50 of ACh alone (8.63 ± 4.38 × 10−9 M). Similarly, the EC 50 of AM in the presence of atropine (3.30 ± 0.39 mg/ml) was significantly higher (P < 0.05) than EC 50 of AM alone (0.78 ± 0.12 mg/ml). The CRC of AM was on the right side of ACh [[Figure 1]c] and the EC 50 of AM (0.78 ± 0.12 mg/ml) was significantly higher (P < 0.05) than that of ACh (1.57 ± 0.8 × 10−6 mg / ml). Moreover, the maximal response of AM (1053.82 ± 18.40 mg) was found to be significantly less (P < 0.05) than that of ACh (1491.01 ± 79.60 mg) [[Figure 1]c]. | Figure 1: Interaction of Aegle marmelos (AM) with Muscarinic receptors. Cumulative concentration-response curves of (a) acetylcholine (Ach) alone and ACh in the presence of atropine (10−7 M) (b) AM alone and AM in the presence of atropine (10−7 M) (c) ACh and AM on isolated rat ileum values are expressed as mean ± standard error of the mean (n = 3)
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Concentration-dependent contractions were induced by 5-HT as well as AM in isolated rat fundus and both showed a right ward shift in CRC in the presence of ketanserin (10−6 M) [[Figure 2]a and b]. The EC 50 of 5-HT after ketanserin (3.6 ± 0.15 × 10−8 M) was significantly higher (P < 0.05) than EC 50 of 5-HT alone (1.0 ± 0.37 × 10−8 M). The EC 50 of AM after ketanserin (10−6 M) (0.62 ± 0.03 mg/ml) was significantly higher (P < 0.05) than EC 50 of AM alone (0.28 ± 0.03 mg/ml). The CRC of AM was shifted to the right side of 5-HT [[Figure 2]c] and the EC 50 of AM (0.28 ± 0.03 mg/ml) was significantly higher (P < 0.05) than that of 5-HT (4.1 ± 1.5 × 10−6 mg / ml). The maximal response of AM (827.44 ± 69.24 mg) was found significantly lesser (P < 0.05) than that of 5-HT (1110.93 ± 35.83 mg) [[Figure 2]c]. | Figure 2: Interaction of Aegle marmelos (AM) with serotonergic receptors. Cumulative concentration-response curves of (a) 5-HT alone and 5-HT in the presence of ketanserin (10−6 M) (b) AM alone and AM in the presence of ketanserin (10−6 M) (c) 5-HT and AM on isolated rat fundus. Values are expressed as mean ± standard error of the mean (n = 3)
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Isoprenaline (10−6 M) exerted relaxant effect of 81.45% on rat tracheal chain precontracted with CCh (10−5 M). In the presence of propranolol (1 ng/ml), the relaxant effect of isoprenaline (10−6 M) was reduced significantly (P < 0.05) to 32.97% [[Figure 3]a]. AM (0.2 mg/ml) produced relaxant effect of 66.81% on CCh (10−5 M) precontracted tracheal chain. The relaxant effect was reduced significantly (P < 0.05) to 36.23% in the presence of propranolol (1 ng/ml) [[Figure 3]b]. | Figure 3: Interaction of Aegle marmelos (AM) with adrenergic receptors. Effect of propranolol on the relaxant effects of (a) isoprenaline (10−6 M) and (b) AM (0.2 mg/ml) on isolated rat trachea precontracted with carbachol (10−5 M). Values are expressed as mean ± standard error of the mean (n = 3)
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| » Discussion | | |
In the present study, the activity of AM was significantly inhibited in the presence of atropine confirming the presence of cholinergic (ACh-like) components in AM. Moreover, the CRC of AM being on the right side of ACh and higher EC 50 of AM than that of ACh indicate lesser potency of AM when compared with ACh and also, the lower maximal response of ileum to AM indicates its lesser efficacy than ACh. The ileum is supplied with cholinergic nerves that produce contractions via muscarinic receptors, and these cholinergic nerves play an important role in the regulation of gastrointestinal motility. [9] The agonistic action of AM on cholinergic receptor may explain the medicinal use of leaves of AM as mild laxative.
The contractile effect of 5-HT on rat fundus is mediated through serotonergic receptors [10] and is competitively blocked by ketanserin. [11] The dose-dependent contractile effect of AM on isolated rat fundus was inhibited significantly by ketanserin confirming its action on serotonergic system as one of the possible mechanisms. It has been reported that methanolic extract of AM leaves possesses potential anxiolytic and antidepressant activities. [12] Further, it has been proposed, that the stimulation of 5-HT 2B receptor produces anxiolysis. [13] The agonistic action of AM on serotonin receptor as demonstrated by this study may explain the basis for reported use of AM in anxiety and depression.
Isoprenaline as well as AM exerted relaxant effects on precontracted (with CCh) isolated rat trachea. Furthermore, the effects of isoprenaline as well as AM on tracheal chain were reduced significantly in the presence of propranolol. Inhibition of relaxant effect in the presence of a β-blocker, shows that AM possesses an adrenergic component, which relaxed the precontracted tracheal muscle. In a previous study, alcoholic extract of leaves of AM showed relaxant effect on guinea pig tracheal chain and the effect was attributed to the presence of one or more antihistaminic constituents. [14] In our study, aqueous extract was investigated and the relaxant effect on rat tracheal chain may be due the presence of some adrenergic components in the plant. It may be hypothesized that AM shows anti-asthmatic activity due to presence of both components, that is, antihistaminic as well as adrenergic.
| » Conclusion | | |
In this preliminary study, it was demonstrated that aqueous extract of AM possesses agonistic activity on cholinergic, serotonergic and adrenergic receptors using isolated rat ileum, fundus and tracheal tissue preparations.
| » References | | |
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[Figure 1], [Figure 2], [Figure 3]
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