- Research article
- Open Access
- Open Peer Review
Cactus (Opuntia humifusa) water extract ameliorates loperamide-induced constipation in rats
- Sung Hee Han†1,
- Kyungmi Park†2,
- Eun Young Kim3,
- So Hyun Ahn3,
- Hyun-Sun Lee4 and
- Hyung Joo Suh5Email author
© The Author(s). 2017
- Received: 4 June 2016
- Accepted: 28 September 2016
- Published: 17 January 2017
Korean cactus Cheonnyuncho (Opuntia humifusa) is rich in pectin, phenols, flavonoids, and minerals such as calcium and phosphorus. Some Koreans drink Cheonnyuncho juice prepared by grinding Cheonnyuncho with water. Cheonnyuncho is well known for its functional properties and antioxidant effects, but its effect on constipation has not been sufficiently studied.
Loperamide (2 mg/kg) was injected subcutaneously to induce constipation in rats. The animals were divided into four groups: a normal group (NOR), constipation control group (CON), and two constipation groups receiving the Cheonnyuncho extract (CE) at two different concentrations in drinking water, 3% (L-CE group) and 6% (H-CE group), for 25 days.
The fecal pellet numbers of NOR and L-CE were significantly increased from 35.67 ± 2.09 (CON) to 50.60 ± 1.38 and 46.50 ± 2.91 after loperamide treatment, respectively (p < 0.05). The water content of fecal excretions was significantly enhanced in only the L-CE group (33.05 ± 0.49%) compared to control (23.38 ± 1.26%) (p < 0.05) after loperamide treatment. The oral intake of CE (L-CE and H-CE groups) significantly increased levels of the intestinal transit ratio (45.25 ± 1.86% and 41.05 ± 2.47%, respectively) compared to the CON group (32.15 ± 2.05%) (p < 0.05). Treatment with the low concentration of CE significantly increased fecal levels of acetic, propionic, butyric, and valeric acids, as well as the total short-chain fatty acid (SCFA) concentration. Histological analyses revealed that the thickness of the distal colon also increased in the CE-treated groups in a dose-dependent manner.
Constipation decreased when CE was fed to the rats. In particular, the fecal pellet number and water content, as well as histological parameters such as distal colon thickness, improved. The CE treatment also increased the fecal SCFA content. These results show that the extract of Cheonnyuncho (O. humifusa) alleviated the symptoms of loperamide-induced constipation.
- Opuntia humifusa
- Gastrointestinal transit
Constipation refers to bowel movements that are infrequent or hard to pass and is a common cause of painful defecation. Severe constipation includes a failure to pass stools or gas and fecal impaction, which can progress to bowel obstruction and become life threatening. Constipation is a symptom with many causes, including mechanical and functional ones . Causes of colonic slow-transit constipation include diet, hormonal disorders such as hypothyroidism, side effects of medications, and infrequently, heavy metal toxicity . Because constipation is a symptom, not a disease, effective treatment of constipation may first require determining the cause. Treatments include changes in dietary habits, laxatives, enemas, biofeedback, and in particular situations, surgery. Constipation is common, and its incidence in the general population varies from 2 to 30% [1, 3, 4].
The food and pharmaceutical industries have expressed an increasing interest in functional materials with biological activities . Naturally derived materials are often as effective in disease control as chemically synthesized materials, and consumer preference is higher for the former because of their low toxicity and fewer side effects .
Medicinal properties of Opuntia humifusa have been explored in recent years [6, 7]. It has been reported that extracts of O. humifusa exhibit anti-inflammatory and radical-scavenging activities by suppressing the expression of inducible nitric oxide synthase, as well as cytokines including interleukin (IL)-6 and IL-1β, in lipopolysaccharide-treated RAW 264.7 cells . Hahm et al.  reported that oral administration of O. humifusa showed antidiabetic activity owing to a decrease in blood glucose levels in streptozotocin-induced diabetic rats, caused by an increase in the relative beta-cell volume in the pancreas . O. humifusa is also a high-fiber source and is characterized by mucilage production. Mucilage, which is a complex of carbohydrates, is classified as a dietary fiber. Its main component is pectin (48.5%), but mucilage also contains arabinose, galactose, galacturonic acid, and rhamnose . O. humifusa is a good source of dietary fiber, and when added to food as a supplement, can provide beneficial health effects and prevent colonic diseases. Oral intake of the fruit or stem of O. humifusa on an empty stomach has been shown to be effective in treating constipation and urination problems, increasing intestinal movement, and improving appetite . However, scientific evidence of the correlation between O. humifusa intake and constipation improvement has not been presented to date. Therefore, it is worth investigating the laxative effects of an extract of the cactus in an animal model of constipation to verify its mechanism of action under physiological conditions. In this study, we investigated the effect of an extract of the cactus on loperamide-induced constipation in rats.
Preparation of Cheonnyuncho water extract
Cheonnyuncho grown in Sejong, Korea, was harvested in October 2014, washed with water, which was then removed with kitchen paper towels, and stored in a refrigerator. The identity of the plant was ascertained morphologically by Prof. K. S. Shin of Kyonggi University, Suwon, Korea. A voucher specimen (KUCHS-2012008) was deposited at the College of Health Sciences, Korea University, Seoul, Korea. The Cheonnyuncho extract (CE) was prepared as described in our previous study . Briefly, cactus cladodes (10.0 kg) were homogenized with 50.0 L of water. Then, the suspension was hydrolyzed with 250 mL of an enzyme solution [pectinase (2400 U/g) and cellulase (1200 U/g), 1:3 (v/v)] at 45 °C for 6 h. The reaction was stopped by heating to 95 °C for 20 min, followed by cooling to room temperature (23 ± 0.5 °C) The resulting crude extract was filtered and lyophilized to a dry powder.
Cheonnyuncho dietary fiber and mucilage analysis
The amounts of soluble dietary fiber (SDF), insoluble dietary fiber (IDF), and total dietary fiber (TDF) were determined by the gravimetric enzymatic method as previously described by Prosky et al. . For the extraction of mucilage, nopal pads were homogenized with water at a ratio of 1:5 by using an Ultra Turrax model T25 basic homogenizer (IKA Works, Wilmington, NC, USA), and then the mixture was filtered through a fine cloth. The resulting solution was concentrated in vacuum and poured into ethanol (1:5, v/v). The precipitate was separated by centrifugation (5000 g, 1 h), dissolved in distilled water, and freeze-dried.
Experimental animal groups
Male Sprague–Dawley rats (n = 24), with an average weight of 170 g, were purchased from Deahan Biolink (Seoul, South Korea) and maintained at animal facilities of Korea University (Seoul, South Korea) after adaptation for 1 week. Each rat was kept in a specific, pathogen-free room at 24 ± 0.5 °C with relative humidity of 50–55% under 12-h day/night cycles. A standard maintenance diet (Purina rodent chow) and water with/without CE were freely provided in the cage for 25 days. All experiments were performed according to the protocols approved by the Institutional Animal Care and Use Committee at Korea University (KUIACUC-2013-198).
The animals were randomly divided into a normal group (NOR) and three experimental groups, a control group (CON), L-CE group (3% CE added to drinking water), and H-CE group (6% CE added to drinking water). There were six animals assigned to each group. The animals in the NOR and CON groups received only water, without CE. In the experimental animals, constipation was induced by loperamide hydrochloride (Sigma Chemical Co., St. Louis, MO, USA) injection after CE intake (L-CE and H-CE groups) or water intake (CON group). The rats were injected with loperamide (2 mg/kg of body weight) in a saline solution subcutaneously twice per day, at 09:00 and 18:00, for 7 days.
Body weight gain, food intake, and food efficiency ratio
We measured the body weight gain and food intake before inducing constipation with loperamide on week 1 of the experiment and then again after inducing constipation. The food efficiency ratio was calculated by dividing the dietary intake by weight gain during the same period.
Wet and dry weight of fecal pellets
The wet and dry weights of fecal pellets of the animals were measured. Fecal samples were collected before the induction of constipation four times every day for 1 week after the experiment started and once every day during the collection period of constipation . We calculated changes in the wet weight of fecal pellets and water content of fecal pellets. The water content was determined by drying fecal pellets at 70 °C for 24 h in an oven and calculating the difference between the weight before and after drying.
To analyze the content of triglycerides, total cholesterol, and high-density lipoprotein (HDL) cholesterol in the serum, the experimental animals were anesthetized on the last day of the experiment, and blood was collected from the abdominal vein via laparotomy. Serum was obtained from the collected blood by centrifugation (2000 g, 10 min) and analyzed by using an automated serum analyzer (Dri-chem 3500i, Fujifilm, Tokyo, Japan). Serum triglycerides, total cholesterol, and HDL cholesterol were measured using the TG-0024, TCHO-0222, and HDL-0233 kits (Fujifilm), respectively.
Gastrointestinal transit ratio
Concentration of short-chain fatty acids
In order to measure the amount of short-chain fatty acids (SCFAs), feces were collected. One gram of feces was extracted with 5 mL of methanol in a conical tube, and the extract was stored at −60 °C until use. The extracted sample was filtered through a 0.45-μm filter (Millipore, MA, USA). The filtrate was analyzed using a DB-FFAP 123–3253 column (50 mm × 0.32 mm i.d., coated with 0.50-μm film; J&W Scientific, Agilent Technologies, Inc., USA) and a gas chromatography system (YL-6100, Yong-Lin Co., Seoul, Korea) equipped with a flame ionization detector and autosampler (HT 300, Toung-Lin Co., Seoul, Korea). The injection amount of the sample was 1 μL, the inlet and detector temperatures were 200 and 240 °C, respectively, and the analysis conditions were as described by Demigne et al. . The content of acetic, propionic, butyric, and valeric acids was obtained from a calibration curve created using a respective standard reagent.
Histology of the distal colon
Intestinal tissue was embedded in paraffin, and tissue sections (5 μm) were deparaffinized with xylene. After deparaffinization, the tissues were treated with ethanol for 5 min. Then, the samples were stained with Alcian blue for 30 min and rinsed with water. After rinsing, the tissues were stained with a nuclear fast red solution for 30 s and re-dehydrated with ethanol. Then, the tissues were dehydrated, washed, and sealed using xylene. Alcian blue-positive intestinal mucosa cells were observed with an optical microscope (Axiovert S100, Zeiss, Bovenden, Germany).
All statistical analyses were performed using the Statistical Package for Social Sciences, version 12.0 (SPSS, Inc., Chicago, IL, USA). Analysis of variance was performed, and differences among samples were determined using Duncan’s multiple range tests at a significance level of p < 0.05. All data were at the 95% significance level and are reported as mean ± standard deviation (SD) values.
Dietary fiber and mucilage content of Cheonnyuncho
Compared with other plants, Opuntia spp. cladodes exhibit very strong physical properties, such as water-holding capacity, swelling, and viscosity. These are attributable to starchy polysaccharides and IDF, which exhibit poor physical properties in hydration treatments [17, 18]. Fiber is an essential component in a healthy diet and is needed to maintain optimal health. However, dietary fiber intake is often insufficient in all populations [19, 20]. For this reason, fiber is a widely used ingredient in the functional food industry.
Total, insoluble, and soluble dietary fiber and mucilage contents of Cheonnyuncho (g/100 g)
Total dietary fiber (TDF)a
Insoluble dietary fiber (IDF)
Soluble dietary fiber (SDF)
58.07 ± 4.48
39.15 ± 0.52
18.92 ± 3.96
64.74 ± 4.67
19.45 ± 2.00
14.74 ± 0.83
4.71 ± 1.17
46.12 ± 2.61
Number of fecal pellets and fecal water content in experimental animals
Effect of CE on intestinal transit ratio
Triacylglycerol, total cholesterol, and HDL cholesterol
Effects of CE on serum triacylglycerol, total cholesterol, and HDL cholesterol levels in the loperamide-induced constipation rat model
78.75 ± 11.90ns
63.00 ± 8.57
61.33 ± 20.96
78.33 ± 26.78
71.20 ± 5.52ns
75.53 ± 9.77
68.09 ± 9.77
67.34 ± 3.00
24.47 ± 2.23ns
24.61 ± 1.70
24.31 ± 2.38
27.32 ± 3.12
Concentrations of SCFAs
Histology of the distal colon
Cheonnyuncho (O. humifusa) is rich in dietary fiber and therefore, the SDF/IDF ratio is as important a nutritional parameter as the TDF content because they cause different physiological effects . SDF usually comprises compounds with high water-holding capacities, which are substrates for intestinal microbiota and contribute to the health status. The CE sample contained 19.45% TDF and 46.12% mucilage (Table 1). The enzyme treatment used for the extraction might have caused hydrolysis of the fiber and decreased the TDF content. The cactus mucilage, which is a polysaccharide complex, is mainly composed of arabinose, galactose, rhamnose, and galacturonic acid . The characteristic sugar composition of the mucilage suggests a strong similarity to pectins, although the former contains lower levels of galacturonic acid . These biological features have all been associated with the prevention of gastrointestinal diseases, colon cancer, and intestinal constipation .
In constipation, fecal parameters such as the fecal pellet number and fecal water content have been used as indices of the effect of laxative agents . The results obtained for the fecal pellet numbers and fecal water content showed that the fecal output, measured by the fecal pellet number and water content, was significantly elevated by the administration of CE (Fig. 1). These results indicated that CE decreased constipation in the loperamide-treated animals. We suggest that dietary fiber, one of the main components of the cactus, may account for this effect. Cacti contain dietary fiber, and beneficial effects of fiber have been reported for hypertension, diabetes, obesity, gastrointestinal disease, hyperlipidemia, and immune function [31–33]. Lee and Hwang  reported that cellulose increases the fecal excretion by increasing the water content, bulk, and viscosity and that both water-soluble and insoluble cellulose increases the fecal excretion . These previous studies provide the rationale for identifying cellulose as an active component of CE against constipation. Cellulose is a matrix that decreases food digestion by coliform bacteria and increases the fecal water content and bulk .
The effect of CE on the intestinal transit ratio may also be explained by the action of the putative active component of CE, cellulose. Soluble fiber has consistently been reported to accelerate peristaltic activity by maintaining higher acidity levels because fiber fermentation results in SCFA production by intestinal coliform bacteria in rats . Generally, the cactus pulp is an important source of pectin, which constitutes up to 70% of its total raw fiber, while the peel and seeds are composed of cellulose, with its levels constituting 71 and 83%, respectively . The intestinal transit ratio increases by activated peristalsis after administration of dietary fiber to rats . Peristalsis and its related physiological/structural changes may be interpreted as the effects of the CE fiber, which induces intestinal transit and prevents constipation.
Our results showed that the triglyceride, total cholesterol, and HDL cholesterol levels were not significantly different among the L-CE, H-CE, and CON groups, which is not unusual. A recent study has reported that pectin reduces cholesterol absorption . According to the report by Ghaffarzadegan et al. , cholesterol and triglyceride levels were affected by pectin, which reduced triglycerides and plasma and liver cholesterol. However, the reduction ratios of triglycerides and cholesterol were significantly influenced by the degree of pectin esterification. Low-methoxylation pectin reduced cholesterol and triglyceride levels in fat-diet–fed rats, unlike high-methoxylation pectin. Thus, the source and type of pectin may affect blood cholesterol.
Our results showed that the contents of acetic, propionic, butyric, and valeric acids increased in the fecal samples. This factor influences the composition and metabolic activity of colonic microbiota. The availability of a particular dietary fiber is important for the formation of SCFAs, with different types of dietary fiber giving rise to different SCFA amounts and profiles during colonic fermentation. An increased amount of SCFAs in the intestine is a suitable environment for the growth of probiotic microorganisms [40, 42, 43]. The formation of SCFAs helps improve regularity and laxation by increasing the fecal weight and bulk and fecal water-holding capacity . Our findings indicated that CE was fermented by colonic bacteria and might have increased the number of beneficial bacteria, simultaneously alleviating constipation and improving the bowel environment. Therefore, it is believed that CE could be used as a good prebiotic.
The observation of intestinal epithelial cells showed that CE affected the mucus cell activity. Dietary fiber increases the amount of colonic mucus . The mucilage activity in the distal colon is decreased by a high-cellulose diet, and the amount of colonic mucin may increase. Thus, the supply of dietary fiber may increase mucus release into the lumen and decrease mucus degradation in the colonic lumen. According to our data, the thickness of the epithelial tissue layer and the density of mucin-containing crypt cells in the rat distal colon decreased upon loperamide treatment in the CON group but recovered appreciably in the CE diet groups.
Our results demonstrate that loperamide-induced constipation was alleviated by the administration of CE to rats. The CE-treated rats showed improved fecal parameters such as the number of fecal pellets, fecal water content, gastrointestinal transit, and SCFA content. Histopathologic evaluation revealed that the supplementation with CE increased the mucus content in epithelial cells of the loperamide-treated rats. Thus, treatment with CE improves constipation through changes to the intestinal environment, including the intactness of the intestinal epithelium and therapy of a disturbed mucosal barrier. Our results demonstrate that Cheonnyuncho (O. humifusa) alleviates the symptoms of loperamide-induced constipation.
This work was supported by the Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries (IPET) through the High Value-Added Food Technology Development Program funded by the Ministry of Agriculture, Food and Rural Affairs (MAFRA) (114037-03-2-HD030).
Availability of data and materials
The data will be accessible by contacting the corresponding author of this study.
SHH and KMP collected the test data, elucidated the results, and drafted the manuscript. Also, SHH and KMP equally contributed to this research as first authors. KMP and HSL participated in the preparation of all Cheonnyuncho samples for this study. EYK and SYA assisted animal tests of this study. HJS planned the research and interpreted the results. All authors read and approved the final manuscript for simission.
The authors declare that they have no competing interests.
Consent for publication
This study did not involve human participants; hence, this information is not relevant.
This study was approved by the Institutional Animal Care and Use Committee at Korea University (License No. KUIACUC-2013-198).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Andromanakos N, Skandalakis P, Troupis T, Filippou D. Constipation of anorectal outlet obstruction: Pathophysiology, evaluation and management. J Gastroenterol Hepatol. 2006;21:638–46.View ArticlePubMedGoogle Scholar
- Sanabria T. Five part herbal cleanse protocol (detoxifying tea, tonifying tea, relaxing tea, parasite tea, intestinal tea) in conjunction with yoga and a vegan alkalinizing food and juice cleanse program. In: Google Patents. 2013.Google Scholar
- Heaton KW, Radvan J, Cripps H, Mountford RA, Braddon FEM, Hughes AO. Defecation Frequency and Timing, and Stool Form in the General-Population–a Prospective-Study. Gut. 1992;33:818–24.View ArticlePubMedPubMed CentralGoogle Scholar
- Sonnenberg A, Koch TR. Epidemiology of constipation in the United States. Dis Colon Rectum. 1989;32:1–8.View ArticlePubMedGoogle Scholar
- Lee NYJC, Byub MW. Application of irradiation technology for development of functional natural materials. Food Ind Nutr. 2005;10:26–31.Google Scholar
- Patel S. Opuntia cladodes (nopal): Emerging functional food and dietary supplement. Mediterr J Nutr Metab. 2014;7:11–9.Google Scholar
- Hahm S-W, Park J, Son Y-S. Opuntia humifusa stems lower blood glucose and cholesterol levels in streptozotocin-induced diabetic rats. Nutr Res. 2011;31:479–87.Google Scholar
- Cho JY, Park SC, Kim TW, Kim KS, Song JC, Kim SK, Lee HM, Sung HJ, Park HJ, Song YB, et al. Radical scavenging and anti-inflammatory activity of extracts from Opuntia humifusa Raf. J Pharm Pharmacol. 2006;58:113–9.View ArticlePubMedGoogle Scholar
- Feugang JM, Konarski P, Zou D, Stintzing FC, Zou C. Nutritional and medicinal use of Cactus pear (Opuntia spp.) cladodes and fruits. Front Biosci. 2006;11:2574–89.Google Scholar
- Lee KSOC, Lee KY. Antioxidative efffect of the fractions extracted from a Cactus Cheonnyuncho (Opuntia humifusa). Korean J Food Sci Technol. 2005;37:474–8.Google Scholar
- Cho IK, Seo KS, Kim YD. Antimicrobial Activities, Antioxidant Effects, and Total Polyphenol Contents of Extracts of Prickly Pear, Opuntia ficus indica. Korean J Food Preserv. 2009;16:953–8.Google Scholar
- Kim JH, Lee HJ, Lee H-S, Lim E-J, Imm J-Y, Suh HJ. Physical and sensory characteristics of fibre-enriched sponge cakes made with Opuntia humifusa. LWT Food Sci Technol. 2012;47:478–84.View ArticleGoogle Scholar
- Prosky L, Asp NG, Schweizer TF, Devries JW, Furda I. Determination of Insoluble, Soluble, and Total Dietary Fiber in Foods and Food-Products–Interlaboratory Study. J Assoc Off Anal Chem. 1988;71:1017–23.PubMedGoogle Scholar
- Wintola OA, Sunmonu TO, Afolayan AJ. The effect of Aloe ferox Mill. in the treatment of loperamide-induced constipation in Wistar rats. BMC Gastroenterol. 2010;10:95–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Yu LL, Liao JF, Chen CF. Anti-diarrheal effect of water extract of Evodiae fructus in mice. Ethnopharmacol. 2000;73:39–45.View ArticleGoogle Scholar
- Demigne CRC. Stimulation of absorption of volatile fatty-acids and minerals in the cecum of rats adapted to a very high-fiber diet. Br J Nutr. 1985;115:53–60.Google Scholar
- Ayadi MA, Abdelmaksoud W, Ennouri M, Attia H. Cladodes from Opuntia ficus indica as a source of dietary fiber: Effect on dough characteristics and cake making. Ind Crop Prod. 2009;30:40–7.View ArticleGoogle Scholar
- Majdoub H, Picton L, Le Cerf D, Roudesli S. Water Retention Capacity of Polysaccharides from Prickly Pear Nopals of Opuntia Ficus Indica and Opuntia Litoralis : Physical–Chemical Approach. J Polym Environ. 2010;18:451–8.View ArticleGoogle Scholar
- Brownlee LA, Havler ME, Dettmar PW, Allen A, Pearson JP. Colonic mucus: secretion and turnover in relation to dietary fiber intake. Proc Nutr Soc. 2003;62:245–9.View ArticlePubMedGoogle Scholar
- Leung FW. Etiologic factors of chronic constipation: review of the scientific evidence. Dig Dis Sci. 2007;52:313–6.View ArticlePubMedGoogle Scholar
- Yoon WB, Hong YK, Jun HI, Cha MN, Kim YS. Flow behaviors of fruit and stem extracts from Korean cactus (Opuntia humifusa). Food Sci Biotechnol. 2014;23:1103–10.View ArticleGoogle Scholar
- Jung EYYS, Suh HJ. Hypocholesterol Effect of Opuntia humifusa Extract on High Cholesterol Diet-induced Hypercholesterolemic Rats. J Korean Soc Food Sci Nutr. 2014;43:485–90.View ArticleGoogle Scholar
- Hu JL, Nie SP, Xie MY. High pressure homogenization increases antioxidant capacity and short-chain fatty acid yield of polysaccharide from seeds of Plantago asiatica L. Food Chem. 2013;138:2338–45.View ArticlePubMedGoogle Scholar
- Osuna-Martínez U, Reyes-Esparza J, Rodríguez-Fragoso L. Cactus (Opuntia ficus-indica): a review on its antioxidants properties and potential pharmacological use in chronic diseases. Nat Prod Chem Res. 2014;2:2–9.Google Scholar
- Burger-van Paassen N, Vincent A, Puiman P, van der Sluis M, Bouma J, Boehm G, van Goudoever H, Van Seuningen I, Renes IB. The Regulation of the Intestinal Mucin MUC2 Expression By Short Chain Fatty Acids: Implications for Epithelial Protection. Biochem J. 2009;420:211–9.View ArticlePubMedGoogle Scholar
- Shiau SY, Ong YO. Effects of Cellulose, Agar and Their Mixture on Colonic Mucin Degradation in Rats. J Nutr Sci Vitaminol. 1992;38:49–55.View ArticlePubMedGoogle Scholar
- Satchithanandam S, Klurfeld DM, Calvert RJ, Cassidy MM. Effects of dietary fibers on gastrointestinal mucin in rats. Nutr Res. 1996;16:1163–77.View ArticleGoogle Scholar
- Lee S-P, Whang K, Ha Y-D. Functional properties of mucilage and pigment extracted from Opuntia ficus-indica. J Korean Soc Food Sci Nutr. 1998;11:821–6.Google Scholar
- Stintzing FC, Schieber A, Carle R. Phytochemical and nutritional significance of cactus pear. Eur Food Res Technol. 2001;212:396–407.View ArticleGoogle Scholar
- Weickert MO, Pfeiffer AF. Metabolic effects of dietary fiber consumption and prevention of diabetes. J Nutr. 2008;138:439–42.PubMedGoogle Scholar
- Whelton SP, Hyre AD, Pedersen B, Yi Y, Whelton PK, He J. Effect of dietary fiber intake on blood pressure: a meta-analysis of randomized, controlled clinical trials. J Hypertens. 2005;23:475–81.View ArticlePubMedGoogle Scholar
- Petruzziello L, Iacopini F, Bulajic M, Shah S, Costamagna G. Review article: uncomplicated diverticular disease of the colon. Aliment Pharmcol Ther. 2006;23:1379–91.View ArticleGoogle Scholar
- Watzl B, Girrbach S, Roller M. Inulin, oligofructose and immunomodulation. Brit J Nutr. 2005;93:S49–55.View ArticlePubMedGoogle Scholar
- Lee HJHE. Effects of alginic acid, cellulose and pectin level on bowel function in Rats. Korean J Nutr. 1997;30:465–76.Google Scholar
- Lupton JR, Morin JL, Robinson MC. Barley Bran Flour Accelerates Gastrointestinal Transit-Time. J Am Diet Assoc. 1993;93:881–5.View ArticlePubMedGoogle Scholar
- Trepel F. Dietary fibre: More than a matter of dietetics. I. Compounds, properties, physiological effects. Wien Klin Wochenschr. 2004;116:465–76.View ArticlePubMedGoogle Scholar
- Fuller S, Beck E, Salman H, Tapsell L. New Horizons for the Study of Dietary Fiber and Health: A Review. Plant Food Hum Nutr. 2016;71:1–12.View ArticleGoogle Scholar
- El Kossori RL, Villaume C, El Boustani E, Sauvaire Y, Mejean L. Composition of pulp, skin and seeds of prickly pears fruit (Opuntia ficus indica sp.). Plant Food Hum Nutr. 1998;52:263–70.View ArticleGoogle Scholar
- Kim MJLS. The effect of dietary fiber on the serum lipid level and bowel function in rats. Korean J Nutr. 1995;28:28–32.Google Scholar
- Ondarza MA. Cactus Mucilages: Nutritional, Health Benefits and Clinical Trials. J Med Biol Sci Res. 2016;2:87–103.Google Scholar
- Ghaffarzadegan T, Marungruang N, Fåk F, Nyman M. Molecular properties of guar gum and pectin modify cecal bile acids, microbiota, and plasma lipopolysaccharide-binding protein in rats. PLoS One. 2016;11(6):e0157427.View ArticlePubMedPubMed CentralGoogle Scholar
- Glenn G, Roberfroid M. Dietary modulation of the human colonic microbiota: introducing the concept of prebiotics. J Nutr. 1995;125:1401–12.Google Scholar
- Gibson G, Macfarlane G, Cummings J. Occurrence of sulphate‐reducing bacteria in human faeces and the relationship of dissimilatory sulphate reduction to methanogenesis in the large gut. J Appl Bacteriol. 1988;65:103–11.View ArticlePubMedGoogle Scholar
- Slavin JL, Savarino V, Paredes-Diaz A, Fotopoulos G. A review of the role of soluble fiber in health with specific reference to wheat dextrin. J Int Med Res. 2009;37:1–17.View ArticlePubMedGoogle Scholar