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1.
J Nutr Biochem ; 20(9): 677-84, 2009 Sep.
Article in English | MEDLINE | ID: mdl-18829284

ABSTRACT

The aim of this study was to explore the relationship between consumption of large doses of lactic acid bacteria (LAB) and the behaviour and brain morphobiochemistry of normal growing rats. Four groups of rats were treated with LAB cultures twice daily for 6 months. The control group received 1 ml of saline per treatment, while two experimental groups received 1 ml of living bacteria (Lactobacillus plantarum and Lactobacillus fermentum, respectively) and the remaining group received a heat-treated (inactivated) L. fermentum culture. After 2 and 6 months of treatment, respectively, eight animals from each group were sacrificed, and specimens were taken for further analyses. The behaviour of the rats was evaluated five times in an open-field test at monthly intervals throughout the study. Lactobacilli treatment for 2 months induced changes in the motoric behaviour of the rats. The concentration of the astrocytesoluble and filament glial fibrillary acidic protein (GFAP) decreased in the posterior part of the hemispheres, including the thalamus, hippocampus and cortex of the rats treated with L. fermentum. A greater decrease in filament GFAP (up to 50%) was shown in the group receiving the live form of L. fermentum. In contrast, the GFAP in the live L. plantarum-treated group increased, showing elevated levels of the soluble and filament forms of GFAP in the posterior part of the hemispheres. A 60-66% decrease in the amount of the astrocyte-specific Ca-binding protein S-100b was shown in the posterior parts of the hemispheres and in the hindbrain of rats given LAB for 2 months. Prolonged feeding with LAB for 4 months up to full adulthood led to a further decrease in astrocyte reaction, reflected as an additional decrease in the amount of soluble GFAP and locomotor activity in all experimental groups. The changes in filament GFAP and S-100b appeared to disappear after prolonged feeding (total of 6 months) with LAB. In summary, LAB dietary treatment affected the ontogenetic development of the astrocytes, with the highest intensity observed in the early stages of rat development. It can be postulated that LAB treatment may play a preventive role in neurological diseases by decreasing astrocyte reaction and, consequently, lowering locomotor activity.


Subject(s)
Brain/physiology , Gastrointestinal Tract/microbiology , Lactobacillus plantarum/physiology , Limosilactobacillus fermentum/physiology , Animals , Astrocytes/physiology , Body Weight , Brain Chemistry , Calcium/metabolism , Cell Adhesion , Cell Adhesion Molecules, Neuronal/analysis , Cytoskeleton/metabolism , Glial Fibrillary Acidic Protein/analysis , Male , Microbial Viability , Motor Activity , Nerve Growth Factors/analysis , Rats , Rats, Sprague-Dawley , S100 Calcium Binding Protein beta Subunit , S100 Proteins/analysis , Time Factors
2.
Br J Nutr ; 101(5): 735-42, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18644165

ABSTRACT

The dietary lectin phytohaemagglutinin (PHA) induces gut growth and precocious maturation in suckling rats after mucosal binding. The present study investigated the dose range in which PHA provokes gut maturation and if it coincided with immune activation. Suckling rats, aged 14 d, were orogastrically fed a single increasing dose of PHA: 0 (control), 2, 10, 50 or 250 microg/g body weight (BW) in saline. The effect on gut, lymphoid organs and appearance of CD3+ (T-lymphocyte) and CD19+ (B-lymphocyte) cells in the small-intestinal mucosa was studied at 12 h (acute) and 3 d (late phase) after treatment. The low PHA doses (2 and 10 microg/g BW) induced intestinal hyperplasia without mucosal disarrangement but did not provoke gut maturation. Only the high PHA doses (50 and 250 microg/g BW) temporarily disturbed the intestinal mucosa with villi shortening and decrease in disaccharidase activities, and later after 3 d provoked precocious maturation, resulting in an increase in maltase and sucrase activities and decrease in lactase activity and disappearance of the fetal vacuolated enterocytes in the distal small intestine. Exposure to the high, but not to the low, PHA doses increased the number of mucosal CD19+ and CD3+ cells in the small intestine after 12 h, a finding also observed in untreated weaned rats aged 21-28 d. In conclusion, there was a dose-related effect of PHA on gastrointestinal growth and precocious maturation that coincided with a rapid expansion of mucosal B- and T-lymphocytes, indicating a possible involvement of the immune system in this process.


Subject(s)
Gastrointestinal Tract/drug effects , Lymphocyte Subsets/drug effects , Phytohemagglutinins/administration & dosage , Animals , Animals, Suckling , Antigens, CD19/analysis , CD3 Complex/analysis , Disease Models, Animal , Dose-Response Relationship, Drug , Gastrointestinal Tract/growth & development , Gastrointestinal Tract/pathology , Hyperplasia/chemically induced , Hyperplasia/immunology , Immunity, Mucosal/drug effects , Intestinal Mucosa/drug effects , Intestinal Mucosa/immunology , Intestine, Small/drug effects , Intestine, Small/immunology , Lymphocyte Activation/drug effects , Lymphocyte Subsets/immunology , Lymphoid Tissue/drug effects , Phytohemagglutinins/pharmacology , Rats , Rats, Sprague-Dawley
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