
@2025 Afarand., IRAN
ISSN: 2252-0805 The Horizon of Medical Sciences 2014;20(2):109-113
ISSN: 2252-0805 The Horizon of Medical Sciences 2014;20(2):109-113
Effect of Hydro-Alcoholic Extract of Nigella sativa on Gastric Acid and Mucus Secretion in Cyclooxygenase Inhibition Condition in Rats
ARTICLE INFO
Article Type
Original ResearchAuthors
Paseban M. (1 )Niazmand S. (*)
Shafei M.N. (1 )
Soukhtanlou M. (2)
(*) Physiology Department, , Medicine Faculty, Mashhad University of Medical Sciences, Mashhad, Iran
(1 ) Physiology Department, Medicine Faculty, Mashhad University of Medical Sciences, Mashhad, Iran
(2) Biochemistry Department, Medicine Faculty, Mashhad University of Medical Sciences, Mashhad, Iran
Correspondence
Address: Physiology Department, Medicine Faculty, Azadi Square, Mashhad, Khorasan Razavi, Iran. Postal Code: 91779-48564Phone: +985118002223
Fax: +985118828564
niazmands@mums.ac.ir
Article History
Received: November 18, 2013Accepted: May 7, 2014
ePublished: July 1, 2014
BRIEF TEXT
Gastric ulcer is due to imbalance between the defense factors of gastric mucosa like mucus secretion, as well as invasive factors like gastric acid secretion [1]. … [2, 3] NSAIDs are administrated for different diseases [4]; however, their complications on stomach and gastrointestinal tract are the main factors limiting the use of these drugs [5]. … [6,7] Medicinal plants have been used for centuries [8]; and Nigella sativa, having many benefits, is currently in use [9]. Thymoquinone, carvacrol, 4-terpincal, and T-anethole are of the main compounds of the herb. Thymoquinone has antioxidant and anticonvulsant properties, and sweeps the free radicals up [9, 14]. According to studies, Nigella sativa seeds have many other properties, including antibacterial [10], relief [11], hypoglycemic [12], smooth muscle relaxant [13], anti-inflammatory [15], anti-worm [16], antihistamines [17], and antihypertensive [18] properties.
Non-declared
The aim of this study was to investigate the effect of hydro-alcoholic extract of Nigella sativa on acid and gastric mucus secretion in cyclooxygenase inhibition conditions.
This is an interventional study.
Wistar male rats (180g to 220g) from Animal Home of Medicine Faculty of Mashhad University of Medical Sciences were studied at the university in 2012-13.
40 rats were brought under study.
During the experiment, the rats were housed in Animal Room of Medical Faculty in a group, under standard criteria, a proper temperature of22±2℃, and 12-hour light/dark cycle. Using maceration method, 50% hydro-alcoholic extract of Nigella sativa was prepared. To evaporate the solvent and obtain the dried extract, the solvent was put into an oven (40℃). To produce different doses (100 mg/kg, 200 mg/kg, and 400 mg/kg), the dried extract was dissolved in the distilled water. The rats were randomly divided into 5 groups of 8, as follows: Positive Control Group: Receiving the distilled water for 5 days and then, receiving Indomethacin at a dose of 35mg/kg. 100-group: Receiving Nigella sativa seed extract at a dose of 100mg/kg for 5 days and then, receiving 35mg/kg Indomethacin 200-group: Receiving Nigella sativa seed extract at a dose of 200mg/kg for 5 days and then, receiving 35mg/kg Indomethacin 400-group: Receiving Nigella sativa seed extract at a dose of 400mg/kg for 5 days and then, receiving 35mg/kg Indomethacin Ranitidine Group: Receiving Ranitidine at a dose of 50mg/kg for 5 days and then, receiving 35mg/kg Indomethacin For the rats and for 5 days, Nigella sativa seed extract and Ranitidine at different doses were orally (by gavage) administrated once a day and twice a day, respectively. Then, at 6th day and after 24-hour fasting, Indomethacin was administrated by gavage to the rats. 6 hour after Indomethacin administration, the rats were anesthetized, using 80mg/kg ketamine and 8mg/kg xylazine; and pyloric section of their stomach was obstructed for one hour, using suture. After one hour, collecting gastric juice, the stomach was removed. The gastric juice was centrifuged for 10 minutes and with a velocity of 2000 rpm. After taking, the solvent on the top of the tube was tilled by 0.01 normal NaOH. The acid normality was computed with N1V1=N2V2 formula. After removing from abdominal cavity, stomach tissue was washed; and gastric mucus was studied. Corne method was used to measure gastric mucus [19]. Data were analyzed, using SPSS 11.5 software. One-way ANOVA and Post-hoc Tukey tests were used to compare the groups.
In spite of statistically insignificance, there was increase in acid out-put in groups receiving the extract (100, 200, and 400mg per kg body weight) and receiving Ranitidine (50mg per kg body weight), than control group did (Diagram 1). There was significant increase in gastric mucus secretion in groups receiving the extract at doses of 100 and 200mg/kg, than control group did (Diagram 2).
… [20-27] The results are consistent with those of another study showing no significant change in free acidity in case of Nigella sativa oil administration to healthy animals, while showing increase in free acidity in animals receiving Nigella sativa oil before gastric ulcer induction [28]. … [29] The results of the present study, showing unsuccessful Ranitidine action to acid secretion reduction, are to some extent consistent with those of another study showing no PH increase by Ranitidine and revealing reduction in Ranitidine effect on gastric acid suppression through inhibition of prostaglandin synthesis by Indomethacin [30].
The produced prostaglandin due to Nigella sativa seed extract in gastric juice and its expression in the stomach tissue ought to be measured. In addition, effects of Nigella sativa seed on pepsin, superoxide dismutase catalase, glutathione, glutathione peroxidase, and myeloperoxidase, as well as expression of anti-apoptotic proteins in gastric ulcer, ought to be investigated.
There was no limitation.
Increasing mucus secretion, Nigella sativa seed extract can protect gastric mucosa against injuries caused by inhibition of cyclooxygenase. Nevertheless, it cannot reduce secretion of the acid increased by Indomethacin.
The researchers feel grateful to the research deputy of Mashhad University of Medical Sciences.
Non-declared
All procedures were approved by Ethics Committee of Mashhad University of Medical Sciences.
The research deputy of Mashhad University of Medical Sciences funded the research.
TABLES and CHARTS
Show attach fileCITIATION LINKS
[1]Goel RK, Bhattacharya SK. Gastroduodenal mucosal defence and mucosal protective agents. Indian J Exp Biol. 1991;29(8):701-14.
[2]Koda-Kimble AN, Alldredge BK. Applied therapeutics: The clinical use of druges. 10th ed. Baltimore: Wolters Kluwer Health/Lippincott Williams & Wilkins; 1978.
[3]Yeomans ND, Naesdal J. Systematic review: Ulcer definition in NSAID ulcer prevention trials. Aliment Pharm Ther. 2008;27(6):465-72.
[4]Chan FK. Helicobacter pylori, NSAIDs and gastrointestinal haemorrhage. Eur J Gastroenterol Hepatol. 2002;14(1):1-3.
[5]Brzozowski T, Konturek PC, Konturek SJ, Brzozowska I, Pawlik T. Role of prostaglandins in gastroprotection and gastric adaptation. J Physiol Pharmacol. 2005;56(5):33-55.
[6]Barrett KE BS, Barman SM, Boitano S, Brooks H. Ganongs review of medical physiology. 24rd ed. New York: Mc Graw Hill; 2010.
[7]Yoshikawa T, Naito Y, Kishi A, Tomii T, Kaneko T, Iinuma S, et al. Role of active oxygen, lipid peroxidation, and antioxidants in the pathogenesis of gastric mucosal injury induced by indomethacin in rats. Gut. 1993;34(6):732-7.
[8]Mir Heydar H. Plant referrences: Use of plants in prevention and treatment of diseases. Tehran: Farhang-e- Eslami; 2003. [Persian]
[9]Hadjzadeh MAR, Mohammadian N, Rahmani Z, Rassouli FB. Effect of thymoquinone on ethylene glycol-induced kidney calculi in rats. Urol J. 2008;5(3):149-55.
[10]Hannan A, Saleem S, Chaudhary S, Barkaat M, Arshad MU. Anti bacterial activity of Nigella sativa against clinical isolates of methicillin resistant Staphylococcus aureus. J Ayub Med Coll Abbottabad. 2008;20(3):72-4.
[11]Al-Naggar TB, Gómez-Serranillos MP, Carretero ME, Villar AM. Neuropharmacological activity of Nigella sativa L. extracts. J Ethnopharmacol. 2003;88(1):63-8.
[12]Al-Hader A, Aqel M, Hasan Z. Hypoglycemic effects of the volatile oil of Nigella sativa. Int J Pharm. 1993;31(2):96-100.
[13]Boskabady MH, Keyhanmanesh R, Ebrahimi Saadatloo MA. Relaxant effects of different fractions from Nigella sativa L. on guinea pig tracheal chains and its possible mechanism(s). Indian J Exp Biol. 2008;46(12):805-10.
[14]Farah N, Benghuzzi H, Tucci M, Cason Z. The effects of isolated antioxidants from black seed on the cellular metabolism of A549 cells. Biomed Sci Instrum. 2004;41:211-6.
[15]Al-Ghamdi MS. The anti-inflammatory, analgesic and antipyretic activity of Nigella sativa. J Ethnopharmacol. 2001;76(1):45-8.
[16]Mahmoud MR, El-Abhar HS, Saleh S. The effect of Nigella sativa oil against the liver damage induced by Schistosoma mansoni infection in mice. J Ethnopharmacol. 2002;79(1):1-11.
[17]El-Dakhakhny M. Studies on the Egyptian Nigella sativa L. IV Some pharmacological properties of seeds active principle in comparison to its dihydro compound and its polymer. Arzneimittelforschung. 1965;15(10):1227-9.
[18]El-Tahir KE, Ashour M, Al-Harbi MM. The cardiovascular actions of the volatile oil of the black seed (Nigella sativa) in rats: Elucidation of the mechanism of action. Gen Pharm Vasc Sys. 1993;24(5):1123-31.
[19]Corne SJ, Morrissy SM, Wood RJ. Proceedings: A method for the quantitive estimation of gastric barrier mucus. J Physiol 1974;242(2):116-7.
[20]Rao CV, Sairam K, Goel RK. Experimental evaluation of Bacopa monnieraon rat gastric ulceration and secretion. Indian J Physiol Pharmacol. 2000;44(1):35-41.
[21]Naito Y, Yoshikawa T. Oxidative stress involvement and gene expression in indomethacin-induced gastropathy. Redox Rep. 2006;11(6):243-53.
[22]Suleyman H, Albayrak A, Bilici M, Cadirci E, Halici Z. Different mechanisms in formation and prevention of indomethacin-induced gastric ulcers. Inflammation. 2010;33(4):224-34.
[23]Venables C. Mucus, pepsin, and peptic ulcer. Gut. 1986;27(3):233-8.
[24]Wallace J, Whittle BJ. Role of mucus in the repair of gastric epithelial damage in the rat. Inhibition of epithelial recovery by mucolytic agents. Gastroenterology. 1986;91(3):603-11.
[25]Cross C, Halliwell B, Allen A. Antioxidant protection: A function of tracheobronchial and gastrointestinal mucus. Lancet. 1984;323(8390):1328-30.
[26]Bandyopadhyay SK, Pakrashi SC, Pakrashi A. The role of antioxidant activity of "Phyllanthus emblica" fruits on prevention from indomethacin induced gastric ulcer. J Ethnopharmacol. 2000;70(2):171-6.
[27]Hoogerwerf WA, Pasricha PJ. Agents used for the control of gastric acidity and treatment of peptic ulcer and gastrooesophageal reflux diseases. Goodman & Gilman’s The Pharmacological Basis of Therapeutics, 10th ed. New York: Mc Graw-Hill; 2001.
[28]El-Dakhakhny M, Barakat M, El-Halim M, Aly SM. Effects of Nigella sativa oil gastric secretion and ethanolinduced ulcer in rats. J Ethnopharmacol. 2000;72(1):299- 304.
[29]Arroyo M-T, Lanas A, Sáinz R. Prevention and healing of experimental indomethacin-induced gastric lesions: Effects of ebrotidine, omeprazole and ranitidine. Eur J Gastroenterol Hepatol. 2000;12(3):313-8.
[30]Terzi Coelho CB, Dragosavac D, Coelho Neto JS, Montes CG, Guerrazzi F, Andreollo NA. Ranitidine is unable to maintain gastric ulcer pH levels above 4 in septic patients. J Crit Care. 2009;24(4):627.e7-627.e13.
[2]Koda-Kimble AN, Alldredge BK. Applied therapeutics: The clinical use of druges. 10th ed. Baltimore: Wolters Kluwer Health/Lippincott Williams & Wilkins; 1978.
[3]Yeomans ND, Naesdal J. Systematic review: Ulcer definition in NSAID ulcer prevention trials. Aliment Pharm Ther. 2008;27(6):465-72.
[4]Chan FK. Helicobacter pylori, NSAIDs and gastrointestinal haemorrhage. Eur J Gastroenterol Hepatol. 2002;14(1):1-3.
[5]Brzozowski T, Konturek PC, Konturek SJ, Brzozowska I, Pawlik T. Role of prostaglandins in gastroprotection and gastric adaptation. J Physiol Pharmacol. 2005;56(5):33-55.
[6]Barrett KE BS, Barman SM, Boitano S, Brooks H. Ganongs review of medical physiology. 24rd ed. New York: Mc Graw Hill; 2010.
[7]Yoshikawa T, Naito Y, Kishi A, Tomii T, Kaneko T, Iinuma S, et al. Role of active oxygen, lipid peroxidation, and antioxidants in the pathogenesis of gastric mucosal injury induced by indomethacin in rats. Gut. 1993;34(6):732-7.
[8]Mir Heydar H. Plant referrences: Use of plants in prevention and treatment of diseases. Tehran: Farhang-e- Eslami; 2003. [Persian]
[9]Hadjzadeh MAR, Mohammadian N, Rahmani Z, Rassouli FB. Effect of thymoquinone on ethylene glycol-induced kidney calculi in rats. Urol J. 2008;5(3):149-55.
[10]Hannan A, Saleem S, Chaudhary S, Barkaat M, Arshad MU. Anti bacterial activity of Nigella sativa against clinical isolates of methicillin resistant Staphylococcus aureus. J Ayub Med Coll Abbottabad. 2008;20(3):72-4.
[11]Al-Naggar TB, Gómez-Serranillos MP, Carretero ME, Villar AM. Neuropharmacological activity of Nigella sativa L. extracts. J Ethnopharmacol. 2003;88(1):63-8.
[12]Al-Hader A, Aqel M, Hasan Z. Hypoglycemic effects of the volatile oil of Nigella sativa. Int J Pharm. 1993;31(2):96-100.
[13]Boskabady MH, Keyhanmanesh R, Ebrahimi Saadatloo MA. Relaxant effects of different fractions from Nigella sativa L. on guinea pig tracheal chains and its possible mechanism(s). Indian J Exp Biol. 2008;46(12):805-10.
[14]Farah N, Benghuzzi H, Tucci M, Cason Z. The effects of isolated antioxidants from black seed on the cellular metabolism of A549 cells. Biomed Sci Instrum. 2004;41:211-6.
[15]Al-Ghamdi MS. The anti-inflammatory, analgesic and antipyretic activity of Nigella sativa. J Ethnopharmacol. 2001;76(1):45-8.
[16]Mahmoud MR, El-Abhar HS, Saleh S. The effect of Nigella sativa oil against the liver damage induced by Schistosoma mansoni infection in mice. J Ethnopharmacol. 2002;79(1):1-11.
[17]El-Dakhakhny M. Studies on the Egyptian Nigella sativa L. IV Some pharmacological properties of seeds active principle in comparison to its dihydro compound and its polymer. Arzneimittelforschung. 1965;15(10):1227-9.
[18]El-Tahir KE, Ashour M, Al-Harbi MM. The cardiovascular actions of the volatile oil of the black seed (Nigella sativa) in rats: Elucidation of the mechanism of action. Gen Pharm Vasc Sys. 1993;24(5):1123-31.
[19]Corne SJ, Morrissy SM, Wood RJ. Proceedings: A method for the quantitive estimation of gastric barrier mucus. J Physiol 1974;242(2):116-7.
[20]Rao CV, Sairam K, Goel RK. Experimental evaluation of Bacopa monnieraon rat gastric ulceration and secretion. Indian J Physiol Pharmacol. 2000;44(1):35-41.
[21]Naito Y, Yoshikawa T. Oxidative stress involvement and gene expression in indomethacin-induced gastropathy. Redox Rep. 2006;11(6):243-53.
[22]Suleyman H, Albayrak A, Bilici M, Cadirci E, Halici Z. Different mechanisms in formation and prevention of indomethacin-induced gastric ulcers. Inflammation. 2010;33(4):224-34.
[23]Venables C. Mucus, pepsin, and peptic ulcer. Gut. 1986;27(3):233-8.
[24]Wallace J, Whittle BJ. Role of mucus in the repair of gastric epithelial damage in the rat. Inhibition of epithelial recovery by mucolytic agents. Gastroenterology. 1986;91(3):603-11.
[25]Cross C, Halliwell B, Allen A. Antioxidant protection: A function of tracheobronchial and gastrointestinal mucus. Lancet. 1984;323(8390):1328-30.
[26]Bandyopadhyay SK, Pakrashi SC, Pakrashi A. The role of antioxidant activity of "Phyllanthus emblica" fruits on prevention from indomethacin induced gastric ulcer. J Ethnopharmacol. 2000;70(2):171-6.
[27]Hoogerwerf WA, Pasricha PJ. Agents used for the control of gastric acidity and treatment of peptic ulcer and gastrooesophageal reflux diseases. Goodman & Gilman’s The Pharmacological Basis of Therapeutics, 10th ed. New York: Mc Graw-Hill; 2001.
[28]El-Dakhakhny M, Barakat M, El-Halim M, Aly SM. Effects of Nigella sativa oil gastric secretion and ethanolinduced ulcer in rats. J Ethnopharmacol. 2000;72(1):299- 304.
[29]Arroyo M-T, Lanas A, Sáinz R. Prevention and healing of experimental indomethacin-induced gastric lesions: Effects of ebrotidine, omeprazole and ranitidine. Eur J Gastroenterol Hepatol. 2000;12(3):313-8.
[30]Terzi Coelho CB, Dragosavac D, Coelho Neto JS, Montes CG, Guerrazzi F, Andreollo NA. Ranitidine is unable to maintain gastric ulcer pH levels above 4 in septic patients. J Crit Care. 2009;24(4):627.e7-627.e13.