Cited by 159Polyamine Metabolism and ApplicationsAnimal Nutrition and PhysiologyClinical Nutrition and Gastroenterology

The DOI matches its Crossref record; 13 of the 14 references it cites were found in a registry or an index.

Spermine and spermidine induce intestinal maturation in the rat

Dufour, C., Dandrifosse, G., Forget, P., Vermesse, F., Romain, N., Lepoint, P.·1988·Gastroenterology

Open this paper in CoChat — free account

Abstract

In the present study, we aimed to induce precocious intestinal maturation in neonatal rats by the oral administration of polyamines. Groups of 5 rats received either saline, spermidine (10 mumol daily), or spermine (6 mumol daily) orally on the 12th, 13th, and 14th postnatal days. The rats were killed on the 15th postnatal day. After the small bowel was removed, a 1-cm distal ileal segment was removed for histologic examination and the remaining small bowel tissue was homogenized for further biochemical analysis. Polyamine administration was shown to induce structural and biochemical mucosal changes characteristic of postnatal maturation. Lactase, sucrase, and maltase specific activities (micromoles of substrate hydrolyzed per minute per gram of protein) were 80 +/- 10, 10 +/- 3, and 116 +/- 19 for the saline-treated rats; 51 +/- 7, 34 +/- 2, and 315 +/- 37 for the spermidine-treated rats; and 25 +/- 2, 46 +/- 5, and 419 +/- 63 for the spermine-treated rats, respectively. Similar results were obtained with rats, first treated with spermine (6 mumol) on the 7th postnatal day, receiving spermine (6 mumol) daily as described above and killed on the 10th postnatal day. Dose-response experiments performed as reported above in rats whose treatment began on the 12th postnatal day showed that the maturational effects of orally administered spermine are dose-dependent.

Integrity signals

Registry

Crossref · 10.1016/0016-5085(88)90298-3

Cites

13 of 13 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302
[99] Determination of nucleic acids in tissues by pentose analysis
Schneider, W. (1957) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(57)03442-4 · Cited by 1,890
Polyamines in rapid growth and cancer
Jänne, J. (1978) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/0304-419x(78)90015-x · Cited by 1,346
Assay of intestinal disaccharidases
Dahlqvist, A. (1968) · Analytical Biochemistry · doi:10.1016/0003-2697(68)90263-7 · Cited by 1,208
Amine synthesis in rapidly growing tissues: ornithine decarboxylase activity in regenerating rat liver, chick embryo, and various tumors.
Russell, D., & Snyder, S. H. (1968) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.60.4.1420 · Cited by 747
Ornithine Decarboxylase Is Important in Intestinal Mucosal Maturation and Recovery from Injury in Rats
Lux, G. D., Marton, L. J., & Baylin, S. B. (1980) · Science · doi:10.1126/science.6774420 · Cited by 347
Influence of Epidermal Growth Factor on the Development of Suckling Mouse Intestinal Mucosa
Malo, C., & Ménard, D. (1982) · Gastroenterology · doi:10.1016/s0016-5085(82)80280-1 · Cited by 194
The Role of Cell Renewal in the Ontogeny of the Intestine. I. Cell Proliferation Patterns in Adult, Fetal, and Neonatal Intestine
Klein, R. M., & McKenzie, J. C. (1983) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-198302010-00004 · Cited by 72
The Role of Cell Renewal in the Ontogeny of the Intestine. II. Regulation of Cell Proliferation in Adult, Fetal, and Neonatal Intestine
Klein, R. M., & McKenzie, J. C. (1983) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-198302020-00002 · Cited by 54
Synergistic Effects of Insulin and Thyroxine on the Differentiation and Proliferation of Epithelial Cells of Suckling Mouse Small Intestine
Malo, C., & Ménard, D. (2009) · Biology of the Neonate · doi:10.1159/000241712 · Cited by 49

Show all 14 references

Sorted by citations

Gut microbiota, metabolites and host immunity
Rooks, M. G., & Garrett, W. S. (2016) · Nature reviews. Immunology · doi:10.1038/nri.2016.42 · Cited by 3,409
Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System
Postler, T. S., & Ghosh, S. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.05.008 · Cited by 876
“Dufour et al., 1988; Levy et al., 2015; Pérez-Cano et al., 2010; Wang et al., 1997; Zhang et al., 1999 Gut Bacteria ty bile l Inhibit NF-kB-dependent transcription of proinflammatory genes in monocytes, macrophages, dendritic cells.”
Background
Toxicological effects of dietary biogenic amines.
Ladero, V., Calles-Enriquez, M., Fernandez, M., & A. Alvarez, M. (2010) · Current Nutrition & Food Science · doi:10.2174/157340110791233256 · Cited by 538
Biological significance of dietary polyamines
Larqué, E., Molina, M. S., & Zamora, S. (2006) · Nutrition · doi:10.1016/j.nut.2006.09.006 · Cited by 311
Effect of live yeast incorporation in compound diet on digestive enzyme activity in sea bass (Dicentrarchus labrax) larvae
Tovar‐Ramírez, D., Zambonino‐Infante, J., Cahu, C. L., Gatesoupe, F.-J., Vázquez‐Juárez, R., & Lésel, R. (2002) · Aquaculture · doi:10.1016/s0044-8486(01)00650-0 · Cited by 277
Polyamines in food—implications for growth and health
Bardócz, S., Grant, G., Brown, D. S., Ralph, A., & Pusztai, A. J. (1993) · The Journal of Nutritional Biochemistry · doi:10.1016/0955-2863(93)90001-d · Cited by 234
Metabolite interactions between host and microbiota during health and disease: Which feeds the other?
Zhang, Y., Chen, R., Zhang, D., Qi, S., & Liu, Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114295 · Cited by 224
Influence of dietary live yeast on European sea bass (Dicentrarchus labrax) larval development
Tovar‐Ramírez, D., Zambonino‐Infante, J., Cahu, C. L., Gatesoupe, F.-J., & Vázquez‐Juárez, R. (2004) · Aquaculture · doi:10.1016/j.aquaculture.2004.01.028 · Cited by 191
Immunonutrition: role of sulfur amino acids, related amino acids, and polyamines
Grimble, R. F., & GRIMBLE, G. K. (1998) · Nutrition · doi:10.1016/s0899-9007(98)80041-5 · Cited by 185
Neonatal short bowel syndrome
Goulet, O., Révillon, Y., Jan, D., Potter, S. D., Maurage, C., Lortat‐Jacob, S., Martelli, H., Nihoul‐Feketé, C., & Ricour, C. (1991) · The Journal of Pediatrics · doi:10.1016/s0022-3476(05)81032-7 · Cited by 175
Saccharomyces boulardii Enhances Rat Intestinal Enzyme Expression by Endoluminal Release of Polyamines
Buts, J., Keyser, N. D., & Raedemaeker, L. D. (1994) · Pediatric Research · doi:10.1203/00006450-199410000-00019 · Cited by 175
Formation, Degradation, and Detoxification of Putrescine by Foodborne Bacteria: A Review
Wunderlichová, L., Buňková, L., Koutný, M., Jančová, P., & Buňka, F. (2014) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12099 · Cited by 166
Polyamines in foods: development of a food database
Ali, M. A., Poortvliet, E., Strömberg, R., & Yngve, A. (2011) · Food & Nutrition Research · doi:10.3402/fnr.v55i0.5572 · Cited by 163
Dietary polyamines are essential luminal growth factors for small intestinal and colonic mucosal growth and development
Löser, C., Eisel, A., Harms, D., & Fölsch, U. R. (1999) · Gut · doi:10.1136/gut.44.1.12 · Cited by 155
Functions and roles of the extracellular Ca2+-sensing receptor in the gastrointestinal tract
Hébert, S., Cheng, S. X., & Geibel, J. P. (2003) · Cell Calcium · doi:10.1016/j.ceca.2003.10.015 · Cited by 140
Maturation of villus and crypt cell functions in rat small intestine: Role of dietary polyamines
Buts, J.-P., De Keyser, N., Kolanowski, J., Sokal, E., & Van Hoof, F. (1993) · Digestive Diseases and Sciences · doi:10.1007/bf01295726 · Cited by 137
Immunomodulation by food: impact on gut immunity and immune cell function
Hachimura, S., Totsuka, M., & Hosono, A. (2018) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2018.1433017 · Cited by 135
The gut ecosystem and immune tolerance
Shao, T., Hsu, R., Rafizadeh, D. L., Wang, L., Bowlus, C. L., Kumar, N., Mishra, J., Timilsina, S., Ridgway, W. M., Gershwin, M. E., et al. (2023) · Journal of Autoimmunity · doi:10.1016/j.jaut.2023.103114 · Cited by 143
The Relationship between Microbiota and Polyamine Concentration in the Human Intestine: A Pilot Study
Matsumoto, M., & Benno, Y. (2007) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2007.tb03887.x · Cited by 129
The Functions and Roles of the Extracellular Ca2+–Sensing Receptor along the Gastrointestinal Tract
Geibel, J. P., & Hébert, S. (2009) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163128 · Cited by 125
Enhanced intestinal synthesis of polyamines from proline in cortisol-treated piglets
Wu, G., Flynn, N. E., & Knabe, D. A. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.279.2.e395 · Cited by 116
Microbiota–Host Transgenomic Metabolism, Bioactive Molecules from the Inside
Turroni, S., Brigidi, P., Cavalli, A., & Candela, M. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00244 · Cited by 111
Polyamines in human and rat milk and in infant formulas
Pollack, P., Koldovska, O., & Nishioka, K. (1992) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/56.2.371 · Cited by 107
Extracellular polyamines regulate fluid secretion in rat colonic crypts via the extracellular calcium-sensing receptor
Cheng, S. X., Geibel, J. P., & Hébert, S. (2003) · Gastroenterology · doi:10.1053/j.gastro.2003.10.064 · Cited by 106
Effects of Saccharomyces boulardii on Intestinal Mucosa
Buts, J., & Keyser, N. D. (2006) · Digestive Diseases and Sciences · doi:10.1007/s10620-005-9016-x · Cited by 104
LKM512 yogurt consumption improves the intestinal environment and induces the T‐helper type 1 cytokine in adult patients with intractable atopic dermatitis
Matsumoto, M., Aranami, A., Ishige, A., Watanabe, K., & Benno, Y. (2007) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2007.02642.x · Cited by 98
Polyamines in human and animal milk
Löser, C. (2000) · British Journal Of Nutrition · doi:10.1017/s0007114500002257 · Cited by 96
Polyamines and the Intestinal Tract
Seiler, N., & Raul, F. (2007) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408360701250016 · Cited by 93
Pharmacological properties of the natural polyamines and their depletion by biosynthesis inhibitors as a therapeutic approach
Seiler, N. (1991) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-7139-6_3 · Cited by 87
Use of Yeasts as Probiotics in Fish Aquaculture
Navarrete, P., & Tovar‐Ramírez, D. (2014) · InTech eBooks · doi:10.5772/57196 · Cited by 81
Saccharomyces boulardii upgrades cellular adaptation after proximal enterectomy in rats
Buts, J.-P., Keyser, N. D., Marandi, S., Hermans, D., Sokal, E. M., Chae, Y.-H. E., Lambotte, L., Chanteux, H., & Tulkens, P. M. (1999) · Gut · doi:10.1136/gut.45.1.89 · Cited by 79
Are milk polyamines preventive agents against food allergy?
Dandrifosse, G., Peulen, O., Khefif, N. E. E., Deloyer, P., Dandrifosse, A.-C., & Grandfils, C. (2000) · Proceedings of The Nutrition Society · doi:10.1017/s0029665100000100 · Cited by 78
Gut-microbiota derived bioactive metabolites and their functions in host physiology
Debnath, N., Kumar, R., Kumar, A., Mehta, P. K., & Yadav, A. K. (2021) · Biotechnology and Genetic Engineering Reviews · doi:10.1080/02648725.2021.1989847 · Cited by 77
The Extracellular Calcium-Sensing Receptor in the Intestine: Evidence for Regulation of Colonic Absorption, Secretion, Motility, and Immunity
Tang, L., Cheng, C. Y., Sun, X., Pedicone, A. J., Mahamadzadeh, M., & Cheng, S. X. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00245 · Cited by 80
Homeostasis in the Gut Microbiota in Chronic Kidney Disease
Bhargava, S., Merckelbach, E., Noels, H., Vohra, A., & Jankowski, J. (2022) · Toxins · doi:10.3390/toxins14100648 · Cited by 77
Health promoting activities of probiotics
Tang, C., & Lu, Z. (2019) · Journal of Food Biochemistry · doi:10.1111/jfbc.12944 · Cited by 68
Intracellular Polyamine Levels of Intestinal Epithelial Cells in Inflammatory Bowel Disease
Weiß, T. S., Herfarth, H. H., Obermeier, F., Ouart, J., Vogl, D., Schölmerich, J., Jauch, K. ‐., & Rogler, G. (2004) · Inflammatory Bowel Diseases · doi:10.1097/00054725-200409000-00006 · Cited by 66
Gut Microbiome Modulates Response to Cancer Immunotherapy
Khan, M. A. W., Ologun, G. O., Arora, R., McQuade, J. L., & Wargo, J. A. (2020) · Digestive Diseases and Sciences · doi:10.1007/s10620-020-06111-x · Cited by 69
Trophic Factors for the Gastrointestinal Tract
Carver, J. D., & Barness, L. A. (1996) · Clinics in Perinatology · doi:10.1016/s0095-5108(18)30242-2 · Cited by 65
Probiotics: The Scientific Evidence in the Context of Inflammatory Bowel Disease
Celiberto, L. S., Bedani, R., Rossi, E. A., & Cavallini, D. (2015) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2014.941457 · Cited by 67
Biogenic Amines Formation Mechanism and Determination Strategies: Future Challenges and Limitations
Ahmad, W., Mohammed, G. I., Al‐Eryani, D. A., Saigl, Z. M., Al-Youbi, A. O., Alwael, H., Bashammakh, A. S., O’Sullivan, C. K., & El-Shahawi, M. S. (2019) · Critical Reviews in Analytical Chemistry · doi:10.1080/10408347.2019.1657793 · Cited by 62
The role of the calcium-sensing receptor in gastrointestinal inflammation
Owen, J. L., Cheng, S. X., Ge, Y., Sahay, B., & Mohamadzadeh, M. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.10.040 · Cited by 61
Spermine Induces Maturation of the Immature Intestinal Immune System in Neonatal Mice
ter Steege, J. C. A., Buurman, W. A., & Forget, P. (1997) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-199709000-00017 · Cited by 59
Improvement of intestinal absorption of water-soluble macromolecules by various polyamines: Intestinal mucosal toxicity and absorption-enhancing mechanism of spermine
Gao, Y., He, L., Katsumi, H., Sakane, T., Fujita, T., & Yamamoto, A. (2007) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2007.11.061 · Cited by 57
Anti-Inflammatory Metabolite Production in the Gut from the Consumption of Probiotic Yogurt ContainingBifidobacterium animalissubsp.lactisLKM512
Matsumoto, M., & Benno, Y. (2006) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.50464 · Cited by 56
Probiotic and nutritional effects of Debaryomyces hansenii on animals
Angulo, M., Reyes‐Becerril, M., Medina-Córdova, N., Tovar‐Ramírez, D., & Angulo, C. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10780-z · Cited by 58
Gastrointestinal immune and microbiome changes during parenteral nutrition
Pierre, J. F. (2017) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00321.2016 · Cited by 57
Dietary polyamines and non-neoplastic growth and disease
Deloyer, P., Peulen, O., & Dandrifosse, G. (2001) · European Journal of Gastroenterology & Hepatology · doi:10.1097/00042737-200109000-00005 · Cited by 53
The Application of Metabolomics to Probiotic and Prebiotic Interventions in Human Clinical Studies
O’Connell, T. M. (2020) · Metabolites · doi:10.3390/metabo10030120 · Cited by 57
Regulation of the intestinal glycoprotein glycosylation during postnatal development: role of hormonal and nutritional factors
Biol, M.-C., & Louisot, P. (2003) · Biochimie · doi:10.1016/s0300-9084(03)00039-7 · Cited by 52
Polyamines in cow's and sow's milk
Motyl, T., Płoszaj, T., Wojtasik, A., Kukulska, W., & Podgurniak, M. (1995) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/0305-0491(95)00010-6 · Cited by 50
Dietary spermine supplementation induces intestinal maturation in sea bass (Dicentrarchus labrax) larvae
Péres, A., Cahu, C. L., & Zambonino‐Infante, J. (1997) · Fish Physiology and Biochemistry · doi:10.1023/a:1007786128254 · Cited by 50
Comparison of Fecal Microbiota and Polyamine Concentration in Adult Patients with Intractable Atopic Dermatitis and Healthy Adults
Matsumoto, M., Kakizoe, K., & Benno, Y. (2007) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2007.tb03888.x · Cited by 49
Effects of dietary polyamines at physiologic doses in early-weaned piglets
Molina, M. S., Larqué, E., Torrella, F., Zamora, J. P., Lozano, T., Muñoz, A., & Zamora, S. (2009) · Nutrition · doi:10.1016/j.nut.2009.01.017 · Cited by 49
Role of calcium and other trace elements in the gastrointestinal physiology
Kirchhoff, P. (2006) · World Journal of Gastroenterology · doi:10.3748/wjg.v12.i20.3229 · Cited by 47
Drug interactions
Boobis, A. R., Watelet, J., Whomsley, R., Benedetti, M. S., Demoly, P. M., & Tipton, K. F. (2009) · Drug Metabolism Reviews · doi:10.1080/10837450902891550 · Cited by 46
Health Benefits of Bovine Colostrum in Children and Adults
Buttar, H. S., Bagwe, S. M., Bhullar, S. K., & Kaur, G. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809868-4.00001-7 · Cited by 45
Molecular aspects of the interaction of spermidine and α-chymotrypsin
Farhadian, S., Shareghi, B., Saboury, A. A., Babaheydari, A. K., Raisi, F., & Heidari, E. (2016) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2016.07.069 · Cited by 40
Polyamines: total daily intake in adolescents compared to the intake estimated from the Swedish Nutrition Recommendations Objectified (SNO)
Ali, M. A., Poortvliet, E., Strömberg, R., & Yngve, A. (2011) · Food & Nutrition Research · doi:10.3402/fnr.v55i0.5455 · Cited by 40
Novel regulatory aspects of the extracellular Ca2+-sensing receptor, CaR
Riccardi, D., Finney, B. A., Wilkinson, W. J., & Kemp, P. J. (2009) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-009-0681-z · Cited by 38
Structural change of myoglobin structure after binding with spermidine
Eslami-Farsani, R., Farhadian, S., Shareghi, B., & Asgharzadeh, S. (2022) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2022.118691 · Cited by 37
Estimation of 24-Hour Polyamine Intake From Mature Human Milk
Dorhout, B., van Beusekom, C. M., Huisman, M., Kingma, A. W., de Hoog, E., Boersma, E. R., & Muskiet, F. A. J. (1996) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-199610000-00015 · Cited by 36
Polyamine Participation in the Maturation of Glycoprotein Fucosylation, but not Sialylation, in Rat Small Intestine
Biol, M.-C., Gréco, S., George, P., Hugueny, I., & Louisot, P. (2002) · Pediatric Research · doi:10.1203/00006450-200205000-00014 · Cited by 35
Coarse Cereals and Legume Grains Exert Beneficial Effects through Their Interaction with Gut Microbiota: A Review
Yao, Z., Cao, Y.-N., Peng, L., Yan, Z., & Zhao, G. (2020) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c05691 · Cited by 35
Enhancement of intestinal absorption of macromolecules by spermine in rats
Sugita, Y., Takao, K., Toyama, Y., & Shirahata, A. (2007) · Amino Acids · doi:10.1007/s00726-007-0532-1 · Cited by 33
Polyamines in Human and Rat Milk Influence Intestinal Cell Growth In Vitro
Capano, G., Bloch, K. J., Carter, E. A., Dascoli, J. A., Schoenfeld, D., & Harmatz, P. (1998) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1002/j.1536-4801.1998.tb01255.x · Cited by 31
Orally administered spermine induces precocious intestinal maturation of macromolecular transport and disaccharidase development in suckling rats
Harada, E., Hashimoto, Y., & Syuto, B. (1994) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(94)90208-9 · Cited by 31
The relationship between spermine content of human milk during the first postnatal month and allergy in children
Peulen, O., Dewé, W., Dandrifosse, G., Henrotay, I., & Romain, N. (1998) · Public Health Nutrition · doi:10.1079/phn19980028 · Cited by 30
Role of interleukin-1β, interleukin-6, and TNF-α in intestinal maturation induced by dietary spermine in rats
Kaouass, M., Deloyer, P., Gouders, I., Peulen, O., & Dandrifosse, G. (1997) · Endocrine · doi:10.1007/bf02738963 · Cited by 30
Analysis of structural and biochemical events occurring in the small intestine after dietary polyamine ingestion in suckling rats
Kaouass, M., Deloyer, P., Wéry, I., & Dandrifosse, G. (1996) · Digestive Diseases and Sciences · doi:10.1007/bf02088570 · Cited by 29
Response of rat immature enterocytes to insulin: Regulation by receptor binding and endoluminal polyamine uptake
Buts, J., Keyser, N. D., Romain, N., Dandrifosse, G., Sokal, E. M., & Nsengiyumva, T. (1994) · Gastroenterology · doi:10.1016/s0016-5085(94)94279-x · Cited by 28
Antiproliferative effect of spermine depletion by N-cyclohexyl-1,3-diaminopropane in human breast cancer cells.
Huber, M., & Poulin, R. (1995) · PubMed · Cited by 27
Putrescine is involved in the vitamin D action in chick intestine
Shinki, T., Tanaka, H., Takito, J., Yamaguchi, A., Nakamura, Y., Yoshiki, S., & Suda, T. (1991) · Gastroenterology · doi:10.1016/0016-5085(91)90590-h · Cited by 27
Spermine affects intestinal in vitro permeability to different-sized molecules in rats
Osman, N., Weström, B. R., Wang, Q., Persson, L., & Karlsson, B. W. (1998) · Comparative Biochemistry and Physiology Part C Pharmacology Toxicology and Endocrinology · doi:10.1016/s0742-8413(98)00042-5 · Cited by 27
Comparison Between the Natural Postnatal Maturation and the Spermine-Induced Maturation of the Rat Intestine
Peulen, O., Pirlet, C., Klimek, M., Goffinet, G., & Dandrifosse, G. (1998) · Archives of Physiology and Biochemistry · doi:10.1076/apab.106.1.46.4392 · Cited by 27
Dietary Spermidine and Spermine Participate in the Maturation of Galactosyltransferase Activity and Glycoprotein Galactosylation in Rat Small Intestine
Gréco, S., Niepceron, E., Hugueny, I., George, P., Louisot, P., & Biol, M.-C. (2001) · Journal of Nutrition · doi:10.1093/jn/131.7.1890 · Cited by 27
Polysaccharides to postbiotics: Nurturing bone health via modulating “gut-immune axis”
Yadav, S., Sapra, L., & Srivastava, R. K. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.134655 · Cited by 29
Polyamines in Goat's Colostrum and Milk
Płoszaj, T., Ryniewicz, Z., & Motyl, T. (1997) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s0305-0491(97)00018-7 · Cited by 26
Cellular Energy Metabolism and Regulation
Kelly, J. M., Summers, M., Park, H. S., Milligan, L. P., & McBride, B. W. (1991) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(91)78215-5 · Cited by 24
Reversibility of spermine-induced intestinal maturation in the rat
Georges, P., Dandrifosse, G., Vermesse, F., Forget, P. P., Deloyer, P., & Romain, N. (1990) · Digestive Diseases and Sciences · doi:10.1007/bf01540571 · Cited by 24
Metabolomic Strategy for the Detection of Metabolic Effects of Spermine Supplementation in Weaned Rats
Liu, G., Fang, T., Yan, T., Jia, G., Zhao, H. Y., Huang, Z., Chen, X., Wang, J., & Bai, X. (2014) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf500882t · Cited by 23
Medicinal Plants, Phytochemicals, and Their Impacts on the Maturation of the Gastrointestinal Tract
Mukonowenzou, N. C., Adeshina, K. A., Donaldson, J., Ibrahim, K. G., Usman, D., & Erlwanger, K. H. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.684464 · Cited by 22
Effect of spermine administration on pancreatic maturation in unweaned rats
Romain, N., Gesell, M. S., Leroy, O., Forget, P. P., Dandrifosse, G., & Luk, G. D. (1998) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/s1095-6433(98)10040-5 · Cited by 22
Intestinal maturation induced by spermine in young animals
Peulen, O., Deloyer, P., Grandfils, C., Loret, S., & Dandrifosse, G. (2000) · Livestock Production Science · doi:10.1016/s0301-6226(00)00218-9 · Cited by 22
Oral administration of deuterium-labelled polyamines to sucking rat pups: luminal uptake, metabolic fate and effects on gastrointestinal maturation
Dorhout, B., Faassen, A. V., van Beusekom, C. M., Kingma, A. W., de Hoog, E., Nagel, G. T., Karrenbeld, A., Boersma, E. R., & Muskiet, F. A. J. (1997) · British Journal Of Nutrition · doi:10.1079/bjn19970180 · Cited by 22
Amines protect in vitro the celiac small intestine from the damaging activity of gliadin peptides
Auricchio, S., de Ritis, G., Vincenzi, M. D., Gentile, V., Maiuri, L., Mancini, E., Porta, R., & Raia, V. (1990) · Gastroenterology · doi:10.1016/0016-5085(90)90473-e · Cited by 22
Premature Stimulation of Rat Sucrase-Isomaltase (SI) by Exogenous Insulin and the Analog B-Asp10 Is Regulated by a Receptor-Mediated Signal Triggering SI Gene Transcription
Buts, J., Duranton, B., Keyser, N. D., Sokal, E. M., Maernhout, A.-S., Raul, F., & Marandi, S. (1998) · Pediatric Research · doi:10.1203/00006450-199805000-00005 · Cited by 22
Intestinal effects of long‐lasting spermine ingestion by suckling rats
Deloyer, P., Peulen, O., & Dandrifosse, G. (2005) · Experimental Physiology · doi:10.1113/expphysiol.2005.031583 · Cited by 21
Polyamide profiles of porcine milk and of intestinal tissue of pigs during suckling
Kelly, D., King, T. P., Brown, D., & McFadyen, M. C. E. (1991) · annales de biologie animale biochimie biophysique · doi:10.1051/rnd:19910107 · Cited by 21
Nutrimetabolomic analysis provides new insights into spermine-induced ileum-system alterations for suckling rats
Liu, G., Yan, T., Fang, T., Jia, G., Chen, X., Zhao, H. Y., Wang, J., & Wu, C. (2015) · RSC Advances · doi:10.1039/c5ra01507c · Cited by 20
Probiotics-induced increase of large intestinal luminal polyamine concentration may promote longevity
Matsumoto, M., & Kurihara, S. (2011) · Medical Hypotheses · doi:10.1016/j.mehy.2011.06.011 · Cited by 20
Moderate Folate Deficiency Influences Polyamine Synthesis in Rats
Sun, D., Stephen, A. M., & Wollin, A. (2002) · Journal of Nutrition · doi:10.1093/jn/132.9.2632 · Cited by 20
Oral administration of spermine advances intestinal maturation in sucking piglets
Cheng, Z., Li, D. F., Xing, J. J., Guo, X. Y., & Li, Z. J. (2006) · Animal Science · doi:10.1079/asc200690 · Cited by 19
Exogenous Spermine Induces Maturation of the Liver in Suckling Rats
Wéry, I., Kaouass, M., Deloyer, P., Buts, J., Barbason, H., & Dandrifosse, G. (1996) · Hepatology · doi:10.1002/hep.510240537 · Cited by 19
Fecal Polyamine Concentration in Children with and without Nutrient Malabsorption
Forget, P., Sinaasappel, M., Bouquet, J., Deutz, N. E. P., & Smeets, C. (1997) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-199703000-00010 · Cited by 19
Polyamine metabolism of enterocyte-like Caco-2 cells after exposure to Phaseolus vulgaris lectin.
Koninkx, J. F. J. G., Brown, D. S., Kok, W., Hendriks, H., Pusztai, A. J., & Bardócz, S. (1996) · Gut · doi:10.1136/gut.38.1.47 · Cited by 19
Microbiota Signals during the Neonatal Period Forge Life-Long Immune Responses
Phillips-Farfán, B. V., Gómez‐Chávez, F., Medina-Torres, E. A., Vargas-Villavicencio, J. A., Carvajal, K., & Camacho, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158162 · Cited by 22
The effects of polyamines on human colonic mucosal function
Rogers, A. C., McDermott, F. D., Mohan, H. M., O’Connell, P. R., Winter, D. C., & Baird, A. W. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.07.006 · Cited by 18
Postnatal intestinal development
Kelly, D., Begbie, R., & King, T. P. (1992) · BSAP Occasional Publication · doi:10.1017/s0263967x00004092 · Cited by 18
Effects of a Single Dose of Orally-Administered Spermine on the Intestinal Development of Unweaned Rate
Wéry, I., Deloyer, P., & Dandrifosse, G. (1996) · Archives of Physiology and Biochemistry · doi:10.1076/apab.104.2.163.12886 · Cited by 18

Authors: Dufour, C., Dandrifosse, G., Forget, P., Vermesse, F., Romain, N., & Lepoint, P.
Affiliations: University of Liège (BE)
ORCID: Romain, N.
Venue: Gastroenterology
Publisher: Elsevier BV
Published: 1988-07
Volume: 95
Issue: 1
Pages: 112-116
ISSN: 0016-5085 (ISSN-L)
DOI: 10.1016/0016-5085(88)90298-3
OpenAlex: W2171807112
Cited by: 158
References: 14
Citations by year: 2024: 1 · 2023: 3 · 2022: 3 · 2021: 7 · 2020: 5 · 2019: 5 · 2018: 3 · 2017: 6 · 2016: 3 · 2015: 4 · 2014: 5 · 2013: 1 · 2012: 1
FWCI: 1.58
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Gastroenterology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Polyamine Metabolism and Applications
Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Nutrition and Physiology
Health Sciences › Nursing › Nutrition and Dietetics › Clinical Nutrition and Gastroenterology
Keywords: spermine, spermidine, polyamines, intestinal maturation, postnatal development, ileum, lactase, sucrase, maltase, brush border enzymes, neonatal rats, dose-response relationship
MeSH terms: Age Factors, Animals, Disaccharidases, DNA, Dose-Response Relationship, Drug, Intestinal Mucosa, Intestines, Proteins, Putrescine, Rats, Inbred Strains, Spermidine, Spermine, Rats

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Spermine and spermidine induce intestinal maturation in the rat

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks