|Year : 2014 | Volume
| Issue : 3 | Page : 204-209
Anti-diarrhoeal investigation from aqueous extract of Cuminum cyminum Linn. Seed in Albino rats
Himanshu Bhusan Sahoo1, Saroj Kumar Sahoo2, Sarada Prasad Sarangi3, Rakesh Sagar4, Mohan Lal Kori5
1 Department of Pharmacology and Experimental Biology, Vedica College of Pharmacy, RKDF University, Bhopal, Madhya Pradesh, India
2 Department of Pharmaceutical Chemistry, Sri Sivani College of Pharmacy, Srikakulam, Andhra Pradesh, India
3 Department of Pharmaceutical Chemistry, Jayamukhi Institute of Pharmaceutical Science, Warangal, Andhra Pradesh, India
4 Department of Pharmacognosy and Phytochemistry, Sri Satya Sai Institute of Pharmaceutical Sciences, Bhopal, Madhya Pradesh, India
5 Department of Pharmacognosy and Phytochemistry, Vedica College of Pharmacy, RKDF University, Bhopal, Madhya Pradesh, India
|Date of Submission||04-Nov-2013|
|Date of Decision||05-Jan-2014|
|Date of Web Publication||16-May-2014|
Dr. Mohan Lal Kori
Department of Pharmacognosy and Phytochemistry, Vedica College of Pharmacy, Bhopal - 462 033, Madhya Pradesh
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Cuminum cyminum Linn. (Umbelliferae), commonly known as Jeera. It is native from mediterranean region, but today widely cultivated in Asian countries. It has been reported to possess various medicinal properties and an important food ingredient. The seed of the plant are claimed for treatment of diarrhoea by various traditional practitioners. Objectives: Hence, the present investigation was undertaken to evaluate aq. extract of C. cyminum seeds (ACCS) against diarrhoea on albino rats. Materials and Methods : The animals were divided into five groups and the control group was applied with 2% acacia suspension, the standard group with loperamide (3 mg/kg) or atropine sulphate (5mg/kg) and three test groups administered orally with 100, 250 and 500 mg/kg of ACCS. The antidiarrhoeal effect was investigated by castor oil induce diarrhoea model, prostaglandin E 2 (PGE 2 ) induced enteropooling model, intestinal transit by charcoal meal test. Results: The ACCS showed significant (P < 0.001) inhibition in frequency of diarrhoea, defecation time delaying, secretion of intestinal fluid as well as intestinal propulsion as compared to control and the graded doses of tested extract followed dose dependent protection against diarrhoea. Conclusions: The study reveals that the ACCS is a potent antidiarrhoeal drug which supports the traditional claim.
Keywords: Antidiarrhoeal effect, castor oil, enteropooling model, Intestinal transit, seed
|How to cite this article:|
Sahoo HB, Sahoo SK, Sarangi SP, Sagar R, Kori ML. Anti-diarrhoeal investigation from aqueous extract of Cuminum cyminum Linn. Seed in Albino rats. Phcog Res 2014;6:204-9
|How to cite this URL:|
Sahoo HB, Sahoo SK, Sarangi SP, Sagar R, Kori ML. Anti-diarrhoeal investigation from aqueous extract of Cuminum cyminum Linn. Seed in Albino rats. Phcog Res [serial online] 2014 [cited 2021 Feb 28];6:204-9. Available from: http://www.phcogres.com/text.asp?2014/6/3/204/132596
| Introduction|| |
Since ancient times, diarrhoea has been recognized as one of the most important health issue world widely, particularly afflicting those populations of socio-economically backward classes and from tribal areas to third-world countries. , Globally, about 2.2 million people have been killed annually by diarrhoea, majority of them are infants and children below the age of 5 years. , According to world health organization, it is the one of the most common cause of morbidity and mortality in many developing countries and became a leading cause of malnutrition in world to-day.  Diarrhoea is characterized by rapid movement of semisolid or watery feacal matter through intestine, three or more times in a day with severe or light abdominal pain and bowel sounds. ,, It was caused either by means of polluted water, consumption of contaminated food and by physical contact like handshake etc., The food or water contamination is mostly due to diarrhoeagenic microorganisms like Escheria coli, Campylobacter jejuni, Vibrio cholera, Giardia intestinalis, Cryptosporidium parvum, Entamoeba histolytica, Cyclospora cayetanensis, viruses like Rota or Adeno and some other species like Salmonella, Shigella, Clostridium etc., These microorganisms cause the influx of water and ions to the intestinal lumen by increasing intestinal motility, thereby causing dehydration of body.  Such type of symptom in diarrhoea is treated by the administration of oral rehydration salts in children or adults to maintain the body fluids osmolality.  Alternatively, some drugs like Diphenoxylate, Loperamide, Diloxanide furoate, Racecadotril, Atropine sulfate etc., are available in the market for treating diarrhoea. But all of the existing drugs suffer from adverse effects like the induction of bronchospasm, vomiting, intestinal obstruction, constipation etc.  In order to overcome these menace of anti-diarrhoeal drugs in world market, the World Health Organization (WHO) has introduced a programme, which encourages towards traditional herbal medicines.  Therefore, there has been great interest in herbal remedies for the treatment of such ailments.
Cuminum cyminum L. is commonly known as 'Jeera' in Hindi, belonging to Umbelliferae family. It is an annual shrub up to 10 to 50cm height, native from the Mediterranean region. The plant is indigenous to Turkistan or northern Egypt, but is today widely cultivated in Pakistan, India, Arabia, UAE, Israel, Iran, Iraq, Yugoslavia, Syria, Bulgaria, Malta, Sudan, Cyprus, China and Java.  Several studies on anti-diabetic,  antioxidant,  anti-bacterial,  anti-fungal,  bronchodilatory,  hepatoprotective and renoprotective,  chemopreventive,  anti-epileptic,  galactagogue,  Hypolipidemic,  male anti-fertility,  memory-enhancing and anti-stress  effect of C. cyminum seed extracts have been reported in literature. The antidiarrhoeal effect of C. cyminum is mentioned in different system of traditional medicine i.e. In Iranian folk medicine,  traditional medicine of Tunisia  and Ayurvedic medicinal system of India.  However, there is no scientific evidence on antidiarrhoeal activity of C. cyminum against above traditional claims so far. Hence, we investigated the antidiarrhoeal activity of C. cyminum seed extract in experimental rats [Figure 1].
| Materials and Methods|| |
Gum acacia, castor oil, charcoal meal (SD Fine chemicals, Mumbai); Lopermaide (Micro labs, Bangalore), Ethanol (Merck, Mumbai); PGE 2 (Astrazeneca, Bangalore) and Ketamine, Atropine Sulphate (Hi Media, Mumbai) were procured. All other reagents and chemicals were of analytical grade.
The dried seeds of Cuminum cyminum were collected from local region of Bhopal, Madhyapradesh, India. Further taxonomic identification and authentification was conducted at the Department of Botany, Dr. H. S. Gour Central University, Sagar, MP, India, where a plant specimen was deposited in the herbarium for further reference.
Preparation of extract
The collected seeds were allowed to shade-dry and powdered to course consistently in a grinder mill. Then the coarse powder was passed through 40 mesh size and stored in an airtight container at room temperature. Accurately 250gm of coarse powder was weighed and extracted in water by adopting a simple maceration procedure at room temperature, for seven days, in conical flasks with occasional shaking and stirring. Then the extract was filtered and concentrated to dryness at room temperature to avoid decomposition. The yield of the extract was found to be 21.49% w/w and preserved in refrigerator for further use. The ACCS was subjected to qualitative analysis for various phytoconstituents.  A known volume of extract was suspended in distilled water and was orally administered to the animals by gastric intubation using a feeding needle during the experimental period.
Adult albino rats (200-250 g) of either sex were procured from the animal house of Vedica College of Pharmacy, Bhopal, India. The study protocol was approved from the Institutional Animal Ethics Committee (IAEC) under the reference no. 1693/PO/a/13/CPCSEA and CPCSEA guidelines were adhered during the maintenance and experiment. All animals were maintained under standard husbandry conditions with food and water ad libitum.
Acute oral toxicity study
The animals were fasted overnight prior to the experiment. Different doses (50-2000 mg/kg, P.O) of the aqueous extract were administered to groups of rats and they were observed continuously for 1 h and then at half-hourly intervals for 4 h, for any gross behavioural changes and further up to 72 h, followed 14 days for any mortality as per the OECD Guideline 425. The seed extract of Cuminum cyminum was found to be non-toxic up to the maximum dose of 2000 mg/kg body weight. Dose selected for antidiarrhoeal evaluation was 100, 250 and 500 mg/kg respectively.
Evaluation of in-vivo antidiarrhoeal activity
Castor oil induced diarrhoea model
Albino wistar strain rats of either sex (150-200 gm) were fasted overnight and divided into five groups (n = 6).  Group I served as control (2% acacia suspension, orally), group II served as standard (Loperamide at a dose of 3 mg/kg orally as suspension) and group III, IV and V were administered the graded dose of ACCS extract (100, 250 and 500 mg/kg respectively). After 60 min of drug treatment, the animals of each group received 1 ml of castor oil orally. The frequency of diarrhoea, wt of faecal material and delay of defecation time was noted up to 4 h in the transparent metabolic cages with pre weighed plastic dishes placed at the base. Weight of plastic dish before and after defecation was noted and compared to control.
Effect on charcoal meal test
Albino wistar rats were treated as described earlier except that Atropine sulfate (5 mg/kg IM) was used as a standard drug.  One hour later after drug treatments, each of these animals were given 1mL of charcoal meal (3% charcoal suspension in 5% suspension of acacia) by oral route to induce diarrhoea. All animals were sacrificed after 30 min; the stomach and small intestine were removed and extended on a clean glass surface. The distance travelled by the charcoal meal from the pylorus to caecum was measured and expressed as a percentage of distance travelled by charcoal plug for each animal.
Prostaglandin E 2 (PGE 2 ) induced enteropooling model
Overnight fasted rats of either sex were divided into six groups; each group carries six animals.  Group I served as negative control (2% acacia suspension orally); group II served as positive control (PGE2 100 μg/kg p.o.); group III, IV and V were received ACCS of 100, 250 and 500 mg/kg P.O. respectively; and group VI served as standard (loperamide 3 mg/kg orally as suspension). After 30 min of extract administration, PGE2 was administered to induce diarrhoea. After two hours of administration of PGE2, each rat was sacrificed by administering excessive dose of ketamine and the small intestine was removed after tying the end with thread and weighed. The intestinal contents were collected by milking into a graduated tube and their volume was measured by measuring cylinder. The intestine was reweighed and the difference between full and empty intestine was calculated.
| Statistical Analysis|| |
The values were expressed as Mean ± SEM of six animals. For statistical analysis of the data, group means were compared by one-way Analysis of variance followed by Dunnett's t'test. Probability values with P < 0.05 were considered as significant. It was carried out with graph pad in Stat 3 software.
| Results|| |
Qualitative phytochemical screening
Phytochemical analysis of the crude eve positive reaction for each of the following secondary metabolites: Alkaloids, Glycosides, Flavonoids, Coumarins, Lignins, Tannins, Terpenoids, Carbohydrates, Protein, fatty acids, phenolic compounds and amino acids.
Effect on castor oil-induced diarrhoea
After administration of castor oil, the diarrhoea was clinically apparent in all the treated groups as compared to control for next 4 h. This was markedly reduction of number of wet faeces as well as frequency of diarrhoea and also observed delay of defecation time. The dose of 500 mg/kg is closer resemblance to the effect of the standard antidiarrhoeal drug as shown in [Table 1].
|Table 1: Effect of aqueous extract of cuminum cyminum seed on castor oil induced diarrhoea in rats|
Click here to view
Effect on charcoal meal test
All the doses of ACCS and atropine sulphate decreased the propulsion of the charcoal meal as compared to control group. The distance travelled by the charcoal meal was found to be 37.81, 39.91 and 44.88% in the ACCS treated groups with the dose of 100, 250, 500 mg/kg respectively; where as the standard showed 50.52%, compared to control group. All these observations were significant (P < 0.001) reduction with dosed dependency in intestinal transit as compared to control. The activity of test extract at dose of 500 mg/kg on charcoal meal test was found to be more effective when compared to atropine, an anticholinergic drug as shown in [Table 2].
|Table 2: Effect of aqueous extract of cuminum cyminum seed on charcoal meal induced peristalsis|
Click here to view
Effect on prostaglandin E 2 induced enteropooling model
The ACCS (100, 250, 500 mg/kg) slowed down the intestinal fluid accumulation by 36.27% to 76.27% in respect to PGE2 treated control group. All the doses of the extract produced a significant (P < 0.001) decrease of intestinal propulsive movement and also dose dependency was observed between the doses of ACCS as shown in [Table 3].
|Table 3: Effect of aqueous extract of cuminum cyminum seed on PGE2 induced enteropooling in rats|
Click here to view
| Discussion|| |
Diarrhoea is usually considered a result of altered motility and fluid accumulation within the intestinal tract. Many antidiarrhoeal agents act by reducing the gastrointestinal motility and its secretions. Castor oil causes diarrhea due to its active metabolite i.e. recinolic acid, which increases peristaltic activity in the small intestine leading to changes in the electrolyte permeability of the intestinal mucosal membrane. The precise mechanism of action of castor oil is through elevated level of prostaglandin biosynthesis. The aq. extract of Cuminum cyminum observed that statistically significant inhibition of the intestinal transit and secretion induced by castor oil in rats. These inhibition may be due to presence of flavonoidal and terpenoidal derivatives, by inhibiting the release of autocoids and prostaglandins in intestinal cells. ,
Phytochemical screening revealed the presence of tannins, alkaloids, glycosides, sugars, terpenes and flavonoids in the aq. extract of Cuminum cyminum. Earlier studies have shown that the anti-dysenteric and anti-diarrhoeal properties of medicinal plants were due to the presence of tannins, alkaloids, saponins, flavonoids, sterols or triterpenes and reducing sugars. , Hence, tannins, reducing sugars, triterpenes and flavonoids may be responsible for the mechanism of action of the anti-diarrhoeal activity of Cuminum cyminum. This could be due to the fact that the aq. extract increased the re-absorption of water by decreasing the intestinal motility as well as intestinal transit in the charcoal meal test. In addition, its antidiarrhoeal action may also be due to the presence of denatured proteins and tannic acid or tannins, which form protein-tannate complex. These complexes coat over the intestinal mucosa and make the mucosa more resistant and hence, reduce secretion and peristaltic movement. ,, The secretory diarrhoea is associated with activation of Cl - channel, results massive secretion of watery diarrhoea from the intestinal lumen. The aq. extract may inhibit the watery secretion from luminal wall by reverting this mechanism. The antidiarrhoeal effect of the aq. extract may be also due to an inhibition of muscle contraction, as observed by charcoal meal and consequently, in a reduction of intestinal propulsion. The inhibition of intestinal muscle contraction is due to presence of flavonoidal constituents. ,, The ACCS resulted in markedly reduction in frequency of diarrhoea, the weight and volume of intestinal contents as well as intestinal transit. The dose of 500 mg/kg of the extract exerted greater antidiarrhoeal effect as comparable to other doses. These results justify the usefulness of ACCS in antidiarrhoeal model as shown in [Figure 2].
|Figure 2: Comparative study of antidiarrhoeal potential of graded dose of ACCS Vs Std drug.|
Click here to view
In summary, the present study revealed that the ACCS showed marked reduction in frequency of diaarrhoeal stool and the reduction in weight and volume of intestinal content, as well as a modest reduction in intestinal transit. The mechanism of antidiarrhoeal effect may be due to reduction of gastrointestinal motility, inhibition of the synthesis of prostaglandin and intestinal muscle contraction. These above mechanisms are due to presence of pharmacologically active substances i.e. tannins, terpenoids and flavonoids etc., Further studies are required to fully investigate the mechanisms responsible for this observed antidiarrhoeal activity.
| Acknowledgement|| |
The authors are extremely thankful to Ayushmati Educational Society, Bhopal, MP and Vice-chancellor of RKDF University, Bhopal, MP for providing financial support and research facilities to conduct this work.
| References|| |
|1.||Fernando C, Ramon A, Halley P. Effect of plants used in Mexico to treat gastrointestinal disorders on charcoal gum acacia induced hyperperistalsis in rats. J Ethnopharmacol 2010;128:49-51. |
|2.||Farthing M, Lindberg G, Dite P, Khalif I, Salazar-Lindo E, Ramakrishna BS, et al. World Gastroenterology Organisation Practice Guidelines: Acute diarrhea, 2008; 1-29. |
|3.||Venkatesan N, Thiyagarajan V, Narayanan S, Arul A, Raja S, Vijaya Kumar SG, et al. Antidiarrhoeal potential of Asparagus racemosus wild root extracts in laboratory animals. J Pharmacol Pharm Sci 2005;8:39-45. |
|4.||Gutierrez RM, Mitchell S, Solis RV. Psidium guajava: A review of its traditional uses, phytochemistry and pharmacology. J Ethnopharmacol 2008;117:1-27. |
|5.||Victoria CG, Bryce J, Fontain O, Monsch R. Reducing deaths from diarrhea through oral rehydration therapy. Bull World Health Organ 2000;78:1246-55. |
|6.||Suleiman MM, Dzenda T, Sani CA. Antidiarrhoeal activity of the methanol stem-bark extract of Annona senegalensis Pers. (Annonaceae). J Ethnopharmacol 2008;116:125-30. |
|7.||Mbagwu HO, Adeyemi OO. Anti-diarrhoeal activity of the aqueous extract of Mezoneuron benthamianum Baill (Caesalpinaceae). J Ethnopharmacol 2008;116:16-20. |
|8.||Ezekwesili CN, Obiora KA, Ugwu OP. Evaluation of the anti-diarrhoeal property of the crude aqueous extract of Ocimum gratissimum L.0 (Labitae) in rats. Biokemistr 2004;16:122-31. |
|9.||Longe RL, Dipiro JT. Diarrhoea and constipation. In: Dipiro JT, Talbert RL, Hayes PE, editors. Pharmacotherapy: A Pathophysiologic Approach. 2 nd ed. New York: Elsevier; 1992. 566-578. |
|10.||Horn R, Perry A, Robinson S. A simple solution. Time 2006;7:42-7. |
|11.||Hardman JG, Limbard LE. The Pharmacological Basis of Therapeutics. In Goodman and Gilman's. 10 th ed. New York: McGraw Hill; 2001. p. 1038. |
|12.||Atta AH, Mouneir SM. Antidiarrhoeal activity of some Egyptian medicinal plant extracts. J Ethnopharmacol 2004;92:303-9. |
|13.||Sebastian P. Ayurvedic Medicine: The Principle of Traditional Practice. 1 st ed. Edinburgh, UK: Churchill Livingstone; 2006. p. 399. |
|14.||Dhandapani S, Subramanian VR, Rajagopal S, Namasivayam N. Hypolipidemic effect of Cuminum cyminum L. on alloxane induced diabetic rats. Pharmacol Res 2002;46:251-5. |
|15.||Jagtap AG, Patil PB. Antihyperglycemic activity and inhibition of advanced glycation end product formation by Cuminum cyminum in streptozotocin induced diabetic rats. Food Chem Toxicol 2010;48:2030-6. |
|16.||Iacobellis NS, Cantore PL, Capasso F, Senatore F. Antibacterial activity of Cuminum cyminum L. and Carum carvi L. essential oils. J Agric Food Chem 2005;53:57-61. |
|17.||Romagnoli C, Andreotti E, Maietti S, Mahendra R, Mares D. Antifungal activity of essential oil from fruits of Indian Cuminum cyminum. Pharm Biol 2010;48:834-8. |
|18.||Boskabady M, Kiani S, Azizi H. Relaxant effect of Cuminum cyminum on guinea pig tracheal chains and its possible mechanism (s). Indian J Pharmacol 2005;37:111-5. |
|19.||Aruna K, Rukkumani R, Varma PS, Menon VP. Therapeutic role of Cuminum cyminum on ethanol and thermally oxidized sunflower oil induced toxicity. Phytother Res 2005;19:416-21. |
|20.||Gagandeep DS, Mendiz E, Rao AR, Kale RK. Chemopreventive effects of Cuminum cyminum in chemically induced forestomach and uterine cervix tumors in murine model systems. Nutr Cancer 2003;47:171-80. |
|21.||Janahmadi M, Niazi F, Danyali S, Kamalinejad M. Effects of the fruit essential oil of Cuminum cyminum Linn.(Apiaceae) on pentylenetetrazol-induced epileptiform activity in F1 neurones of Helix aspersa. J Ethnopharmacol 2006;104:278-82. |
|22.||Agrawala IP, Achar MV, Boradkar RV, Roy N. Galactagogue action of Cuminum cyminum and Nigella staiva. Indian J Med Res 1968;56:841-4. |
|23.||Dhandapani S, Subramanian VR, Rajagopal S, Namasivayam N. Hypolipidemic effect of Cuminum cyminum L. On alloxan-induced diabetic rats. Pharmacol Res 2002;46:251-5. |
|24.||Gupta RS, Saxena P, Gupta R, Kachhawa JB. Evaluation of reversible contraceptive activities of Cuminum cyminum in male albino rats. Contraception 2011;84:98-107. |
|25.||Koppula S, Choi DK. Cuminum cyminum extract attenuates scopolamine induced memory loss and stress-induced urinary biochemical changes in rats: A noninvasive biochemical approach. Pharm Biol 2011;49:702-8. |
|26.||Zargari A. Medicinal plants. Vol. 2. Tehran: Tehran University Press; 1989. p. 519-21. |
|27.||Johri RK. Cuminum cyminum and Carum carvi: An update. Pharmacogn Rev 2011;5:63-72. |
|28.||Anonymous. The Ayurvedic Pharmacopoeia Of India. Part 1. Vol. 1. Government of India, Ministry of Health and Family Welfare, Department of Ayush; 1986. p. 142-3. |
|29.||Evans WC. Trease and Evans' Pharmaconosy. 15 th ed. London: W.B. Saunders Company Ltd.; 2005. |
|30.||Dangi SY, Jolly CI, Narayanan S. Antihypertensive activity of the total alkaloids from the leaves of Moringa oleifera. Pharm Biol 2002;40:144-8. |
|31.||Rouf AS, Islam MS, Rahman MT. Evaluation of antidiarrhoeal activity Rumex maritimus root. J Ethnopharmacol 2003;84:307-10. |
|32.||Biswas S, Murugesan T, Sinha S, Maiti K, Gayen JR, Pal M, et al. Antidiarrhoeal activity of Strychnos potatorum seed extract in rats. Fitoterapia 2002;73:43-7. |
|33.||Nikiéma JB, Vanhaelen-Fastré R, Vanhaelen M, Fontaine J, De Graef C, Heenen M. Effects of antiinflammatory triterpenes isolated from Leptadenia hastata latex on keratinocyte proliferation. Phytother Res 2001;15:131-4. |
|34.||Veiga VFJ, Zunino L, Calixto JB, Patitucci ML, Pinto AC. Phytochemical and antioedematogenic studies of commercial copaiba oils available in Brazil. Phytother Res 2001;15:476-80. |
|35.||Hari JR, Lakshmi. Anti-diarrhoeal activity of the aqueous extract of the bark of cinnamomum zeylanicum linn in mice. J Clin Diagn Res 2012;6:215-9. |
|36.||Longanga OA, Vercruysse A, Foriers A. Contribution to the ethno botanical, phytochemical and pharmacological studies of traditionally used medicinal plants in the treatment of dysentery and diarrhea in the Lamella area, Democratic Republic of Congo (DRC). J Ethanopharmacol 2000;71:411-23. |
|37.||Sharma P, Vidyasagar G, Singh S, Ghule S, Kumar B. Antidiarrhoeal activity of leaf extract of celosia argentea in experimentally induced diarrhoea in rats. J Adv Pharm Technol Res 2010;1:41-8. |
|38.||Macauder PJ. Flavonoids affect acetylcholine, prostaglandin E and antigen mediated muscle contration. Prog Clin Biol Res 1986;231:489-92. |
|39.||Yu LL, Liao JF, Chen CF. Anti-diarrhoeal effect of water extract of Evodiae fructus in mice. J Ethnopharmacol 2000;73:39-45. |
|40.||Capasso F, Pinto A, Mascolo N, Autore G, Franco MP. Effect of flavonoids on PGE 2 and LTD 4-induced contractions on the guinea pig isolated ileum. Pharmacol Res Commun 1988;20 Suppl 1:S201-2. |
|41.||Di Carlo G, Autore G, Izzo AA. Inhibition of intestinal motility and secretory by flavonoids in mice and rats: Structure activity relationships. J Pharm Pharmacol 1993;45:1054-9. |
|42.||Niemegeers CL, Lenaerts FZ, Janseen PA. Loperamide R- 18553, a novel type of anti- diarrhoeal agent. Part 1: In vitro to oral pharmacology and acute toxicity. Comparison with morphine, codein, diphenoxylate and difenoxine. Arzeimittelforsc 1974;24:1633-6. |
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]