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1.
J Nutr Sci ; 10: e25, 2021.
Article in English | MEDLINE | ID: mdl-33996038

ABSTRACT

The relationship of chronotype differences with dietary habits and health-related outcomes among elderly people is not fully understood, although sex and generation differences are observed in human chronotype. Accordingly, we analysed the association of chronotype (as assessed by the midpoint of sleep) with dietary intake and health-related quality of life (HRQoL) in elderly Japanese women. The subjects in this cross-sectional study were 1618 women aged 65 years and older who were grandmothers or acquaintances of dietetics students. The subjects were classified into quintiles with respect to the midpoint of sleep, from the earliest to the latest quintile. HRQoL was assessed by the Japanese version of the short-form 36-item health survey score. Mental health was assessed by the Center for Epidemiologic Studies Depression (CES-D) Scale. Dietary intake was assessed by a brief-type self-administered diet history questionnaire. A later midpoint of sleep was associated with a lower intake of vitamin D and a higher intake of bread and caffeinated drinks. No correlations were observed between chronotype and other nutrient and food intake. The subjects with a late midpoint of sleep (eveningness) showed poor general health perception (GH) and high CES-D scores. Other HRQoL scores did not differ among groups with different midpoints of sleep. In conclusion, chronotype as assessed by the midpoint of sleep is associated with poor GH and depressive tendencies in elderly Japanese women. Additionally, a few associations were found between dietary intake and chronotype in elderly Japanese women.


Subject(s)
Biological Clocks/physiology , Diet , Quality of Life , Sleep , Aged , Cross-Sectional Studies , Eating , Female , Humans , Japan/epidemiology
2.
Nutr Neurosci ; 18(3): 110-7, 2015 Apr.
Article in English | MEDLINE | ID: mdl-24621067

ABSTRACT

OBJECTIVES: This study examined heat shock protein (HSP) 70 expression and rhythms of drinking behavior and locomotor activity in obesity, in order to clarify the involvement of HSPs in obesity-induced disturbance of circadian rhythms. METHODS: C57BL/6J ob/ob mice were used as a murine model of severe obesity. Drinking behavior and locomotor activity of male C57BL/6J (control) mice and ob/ob mice were recorded with the behavioral analyzing system. HSP70 concentration in the homogenized supernatant of each tissue, including the brain, liver, and kidney, was measured by an enzyme-linked immunosorbent assay. RESULTS: We observed an attenuated locomotor activity rhythm in the ob/ob mice compared with the control mice at 13 weeks of age and especially at 27 weeks of age. The drinking rhythm was little affected by obesity. HSP70 protein expression was reduced in the brain and kidney of the ob/ob mice compared with the control mice. However, HSP70 expression in the liver was not altered. DISCUSSION: This study suggests that the obesity-induced reduction of HSP70 expression in the brain and kidney can be directly or indirectly associated with disturbance of rhythms of the master clock and peripheral clocks. The study provides a link between circadian rhythm and HSP expression in obesity; the disturbance of these factors may lead to the progression of metabolic disorders.


Subject(s)
Circadian Rhythm/physiology , Drinking Behavior , Heat-Shock Proteins/metabolism , Motor Activity , Obesity/metabolism , Obesity/psychology , Animals , Behavior, Animal , Brain/metabolism , Disease Models, Animal , Kidney/metabolism , Liver/metabolism , Locomotion , Male , Mice , Mice, Inbred C57BL , Mice, Obese
3.
Nutrition ; 28(11-12): 1109-14, 2012.
Article in English | MEDLINE | ID: mdl-23044162

ABSTRACT

OBJECTIVE: We assessed whether disease activity was associated with dietary habits, nutritional status, adipokines, and oxidative stress in patients with rheumatoid arthritis. METHODS: The subjects were 37 patients with RA. The assessment of the nutritional status included anthropometric and biochemical parameters. A food-frequency questionnaire and a 3-d diet record to assess dietary intake were used. The serum levels of adipokines and oxidative stress markers in sera and saliva were measured. The disease activity was determined using the 28 Disease Activity Score (DAS28). We divided the subjects into high (DAS28 ≥3.2) and low (DAS28 <3.2) disease activity groups. RESULTS: The serum leptin and albumin levels were significantly lower, whereas the inflammatory markers were increased, in the high disease activity group. The dietary intake assessment showed a lower intake of fish oil and a lower ratio of monounsaturated fatty acid intake in the high disease activity group. There was a negative correlation between the DAS28 and the dietary intake of the ratio of monounsaturated fatty acid to total fatty acid intake. The serum oxidative stress marker (reactive oxygen metabolites) showed a positive correlation to the DAS28. The salivary reactive oxygen metabolites also correlated with C-reactive protein and serum reactive oxygen metabolites. CONCLUSION: Altered serum adipokine levels with decreased albumin may reflect the deterioration that is associated with rheumatoid arthritis. An increased oxidative stress was observed in sera and saliva. Intakes of ω-3 polyunsaturated fatty acids, fish oil, and monounsaturated fatty acid seem to affect disease activity and may have beneficial effects by decreasing inflammation.


Subject(s)
Adipokines/metabolism , Arthritis, Rheumatoid/metabolism , Arthritis, Rheumatoid/physiopathology , Diet/adverse effects , Inflammation Mediators/metabolism , Nutritional Status , Oxidative Stress , Adipokines/blood , Aged , Arthritis, Rheumatoid/diet therapy , Arthritis, Rheumatoid/ethnology , Biomarkers/blood , Biomarkers/metabolism , Diet/ethnology , Fatty Acids, Monounsaturated/administration & dosage , Fatty Acids, Monounsaturated/therapeutic use , Fatty Acids, Omega-3/administration & dosage , Fatty Acids, Omega-3/therapeutic use , Feeding Behavior/ethnology , Female , Fish Oils/administration & dosage , Fish Oils/therapeutic use , Humans , Hypoalbuminemia/etiology , Hypoalbuminemia/prevention & control , Inflammation Mediators/blood , Japan , Male , Middle Aged , Nutritional Status/ethnology , Reactive Oxygen Species/blood , Reactive Oxygen Species/metabolism , Saliva/metabolism , Severity of Illness Index
4.
Int J Food Sci Nutr ; 62(5): 525-32, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21495902

ABSTRACT

We analyzed the association between dietary intake and chronotype as assessed by both Morningness-Eveningness Questionnaire (MEQ) score and preferred midpoint of sleep in 112 young Japanese women. Dietary intake was assessed by a brief, self-administered diet history questionnaire. A lower MEQ score (evening-type tendency) showed a significant association with a lower energy-adjusted intake of protein, calcium, magnesium, zinc, vitamins (D, riboflavin, and B(6)), and vegetables, and with a higher intake of noodles. Furthermore, a later midpoint of sleep showed a significant association with a lower energy-adjusted intake of protein, cholesterol, potassium, calcium, magnesium, zinc, vitamins (D, riboflavin, B(6), and B(12)), soy, fish and shellfish, and eggs, and with a higher intake of noodles, bread, and confections. These data suggest that evening chronotype is associated with inadequate dietary habits such as low vitamin and mineral intakes.


Subject(s)
Biological Clocks/physiology , Eating , Feeding Behavior/physiology , Sleep/physiology , Adolescent , Diet , Energy Intake , Female , Humans , Japan , Nutrition Surveys , Young Adult
5.
Sleep Med ; 12(3): 289-94, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21296614

ABSTRACT

OBJECTIVES: How human chronotype is correlated to nutrient and food-group intakes and dietary behavior remains to be elucidated. We cross-sectionally examined the association between the midpoint of sleep and these dietary variables in young Japanese women. A calculated halfway point between bedtime and rise time was used as midpoint of sleep. METHODS: The subjects were 3304 female Japanese dietetics students aged 18-20years from 53 institutions in Japan. Dietary intake during the previous month was assessed by a validated, self-administered diet history questionnaire. The midpoint of sleep was calculated using self-reported bedtimes and rise times. RESULTS: Late midpoint of sleep was significantly negatively associated with the percentage of energy from protein and carbohydrates, and the energy-adjusted intake of cholesterol, potassium, calcium, magnesium, iron, zinc, vitamin A, vitamin D, thiamin, riboflavin, vitamin B(6), folate, rice, vegetables, pulses, eggs, and milk and milk products. It was also significantly positively associated with the percentage of energy from alcohol and fat, and the energy-adjusted intake of noodles, confections, fat and oil, and meat. Furthermore, subjects with a later midpoint of sleep tended to begin meals later, eat for a longer time, skip meals more frequently, and watch TV at meals, not only at breakfast but also at lunch and dinner. CONCLUSIONS: The midpoint of sleep is significantly associated with dietary intake of certain nutrients and foods and other dietary behaviors in young Japanese women. This finding may contribute to consider the relationships between chronotype and dietary intakes and behaviors.


Subject(s)
Circadian Rhythm/physiology , Eating/physiology , Feeding Behavior/physiology , Sleep/physiology , Adolescent , Asian People , Cross-Sectional Studies , Dietary Carbohydrates/administration & dosage , Dietary Fats/administration & dosage , Dietary Proteins/administration & dosage , Energy Metabolism/physiology , Female , Humans , Surveys and Questionnaires , Television , Young Adult
6.
Obesity (Silver Spring) ; 18(9): 1688-94, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20111014

ABSTRACT

Few reports show whether a high-fat (HF) dietary environment in the fetal period affects immune function or the development of lifestyle-related disease at maturity. We examined the influence of an HF dietary environment in the fetal period on postnatal metabolic and immune function. A total of 16 pregnant mice were given control (CON) diet and 16 were given HF diet in the gestational period, from mating to delivery. After delivery lactating mice were given either CON or HF diet, resulting in four groups. After weaning, the offspring mice were given the same diet that their mothers received during lactation. HF dietary intake in the postnatal period increased fat pad weights, serum glucose, and leptin levels. An HF diet in the fetal period resulted in fewer splenic lymphocytes, a thinner thymic cortex, and impaired antigen-specific immune reactions. Furthermore, tumor necrosis factor (TNF)-alpha production and serum triglyceride levels were elevated in the fetal HF group. In addition, the HF-HF group showed a consistent decrease in ovalbumin (OVA)-specific IgG and elevation of IgE, associated with advanced fatty changes in the liver. Results from this study suggest that HF environment during the fetal period induces epigenetic propensity toward obesity and immunological burden in part due to increased adipose tissue mass, significant reduction in the number of immune cells and decreased activities of immune cells.


Subject(s)
Adipose Tissue/metabolism , Blood Glucose/metabolism , Dietary Fats/pharmacology , Immunity/drug effects , Lymphocytes/metabolism , Prenatal Exposure Delayed Effects , Triglycerides/blood , Adipose Tissue/pathology , Animals , Environment , Epigenesis, Genetic , Fatty Liver/etiology , Fatty Liver/pathology , Female , Immunoglobulin E/blood , Immunoglobulin G/blood , Leptin/blood , Male , Mice , Mice, Inbred C57BL , Ovalbumin/immunology , Pregnancy , Prenatal Exposure Delayed Effects/blood , Prenatal Exposure Delayed Effects/immunology , Spleen/immunology , Spleen/pathology , Thymus Gland/pathology , Tumor Necrosis Factor-alpha/metabolism
7.
J Nutr ; 138(6): 1192S-8S, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18492856

ABSTRACT

In the early 1980s the Japanese scientific academy defined a functional food as a food having a tertiary or physiologically active function. The current Japanese "Food with Health Claims" include 2 categories. For the first category, "Food with Nutrient Function Claims," the label may be freely used if a product satisfies the standard for the minimum and maximum levels per daily portion usually consumed. The second category is defined as "Food for Specified Health Uses" (FOSHU). FOSHU foods are those that contain dietary ingredients that have beneficial effects on the physiological functions of the human body, maintain and promote health, and improve health-related conditions. Health claims on these foods correspond to the category of "other" function claims of the Codex Alimentarius. However, claims of disease-risk reduction are not currently allowed under FOSHU with an exception for calcium and folic acid. Manufacturers can emphasize the characteristics of their products and promote sales by labeling or claims. Therefore, the labeling should be clear and correct and avoid any chance of misinterpretation. The labeling of health claims on foods should always be based on scientific evidence. Any manufacturer who applies to the government for approval under the FOSHU code for its product must tabulate both published available publications and internal reports on the effectiveness of the product and/or its ingredients and provide a summary of each available publication or report. The tabulation must include in vitro metabolic and biochemical studies, in vivo studies, and randomized controlled trials on Japanese people. The overall philosophy of the Ministry is to maintain and improve the health status of people and to prevent chronic noncommunicable diseases through an approach that involves a well-balanced diet as well as through the use of "health foods" including "Food with Health Claims."


Subject(s)
Food Labeling/legislation & jurisprudence , Food, Organic/standards , Food Labeling/standards , Health Occupations , Humans , Information Services , Japan , Legislation, Food/standards , Minerals , Public Policy , Vitamins
8.
Eur J Nutr ; 46(5): 300-6, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17623226

ABSTRACT

BACKGROUND: Adequate folate status in pregnancy is important for satisfactory pregnancy outcome. AIM OF THE STUDY: The objective of the present study was to evaluate folate status in healthy pregnant women by assessing dietary folate intakes and measuring changes in folate-related biomarkers including plasma tHcy, serum vitamin B(12) (B(12)), and serum and RBC folate concentrations in each trimester and to examine their relation to fetal growth. METHODS: From 94 pregnant women, 3-day-dietary records were obtained and blood was collected for plasma total homocysteine (tHcy), serum B(12), and serum and red-blood cell (RBC) folate measurements. Infant anthropometric measurements were made immediately after birth. RESULTS: Average folate intake was less than 300 microg/day with a mean energy intake of about 1800 kcal. Mean serum and RBC folate concentrations declined significantly during gestation (p < 0.05). Mean serum B(12) also significantly decreased (p < 0.01), whereas plasma tHcy increased from 5.1 in the first trimester to 5.9 micromol/l in the third trimester (p < 0.01). Multiple regression analyses, after controlling for maternal age, parity and pre-pregnancy body-mass index indicated that a 1.0 micromol/l increase in plasma tHcy in the third trimester corresponded to a 151 g decrease in birth weight (p < 0.01). Neither B(12) nor folate concentrations in all three trimesters showed any significant associations with birthweight. Plasma pyridoxal-5'-phosphate concentrations were markedly low, and were consistent with low intake of vitamin B(6) in our population. CONCLUSION: Our data suggest that higher plasma tHcy in the third trimester is a predictor of lower birth weight. In general, the dietary intake of B-vitamins and energy may be inadequate in our population, suggesting intervention is necessary.


Subject(s)
Fetal Development/physiology , Folic Acid/administration & dosage , Folic Acid/blood , Homocysteine/blood , Nutritional Status , Adult , Biomarkers/blood , Birth Weight , Body Mass Index , Erythrocytes/chemistry , Female , Fetal Development/drug effects , Humans , Infant, Newborn , Japan/epidemiology , Male , Parity , Pregnancy , Pregnancy Outcome , Vitamin B 12/blood , Vitamin B Complex/administration & dosage , Vitamin B Complex/blood
9.
J Biol Rhythms ; 22(4): 312-23, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17660448

ABSTRACT

Energy homeostasis is subjected to a circadian control that synchronizes energy intake and expenditure. The transcription factor CLOCK, a key component of the molecular circadian clock, controls many kinds of rhythms, such as those for locomotor activity, body temperature, and metabolic functions. The purpose of the present study is to understand the function of the Clock gene during lipid metabolism in the liver using Clock-mutant mice. Clock-mutant mice with an ICR background were fed a high-fat diet for 13 weeks, and liver triglyceride, serum triglyceride, and serum free fatty acid levels were examined. Triglyceride content in the liver was significantly less increased in Clock-mutant mice on a high-fat diet compared to wild-type mice on a high-fat diet. Acsl4 and Fabp1 mRNA levels in the liver showed daily rhythms in wild-type mice. In contrast, Clock -mutant mice had attenuated daily rhythms of Acsl4 and Fabp1 gene expression in the liver under both normal and high-fat diet conditions compared to wild-type mice. In Clock-mutant mice, suppression of Acsl4 and Fabp1 mRNA in the liver under high-fat diet conditions may have attenuated the accumulation of triglycerides in the liver compared to wild-type mice under the same conditions. In conclusion, the authors demonstrate that mice with a Clock mutation showed less triglyceride accumulation in the liver through the suppression of Acsl4 and Fabp1 gene expression when fed a high-fat diet compared to wild-type mice fed the same diet.


Subject(s)
Circadian Rhythm/physiology , Dietary Fats/administration & dosage , Fats/pharmacology , Gene Expression Regulation/drug effects , Triglycerides/blood , Animals , CLOCK Proteins , Dietary Fats/metabolism , Fatty Acids/analysis , Fatty Acids/metabolism , Gene Expression Regulation/genetics , Liver/drug effects , Liver/metabolism , Mice , Mice, Inbred ICR , Time Factors , Trans-Activators
10.
Nutrition ; 23(4): 342-50, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17367996

ABSTRACT

OBJECTIVE: Protein-energy malnutrition (PEM) is a serious nutritional problem that causes immune dysfunction in elderly people. Probiotic lactic acid bacteria may potentially modify immunity; however, there is little evidence to elucidate the influence of these bacteria on PEM in the elderly. METHODS: The immune modulation effects of lactic acid bacterium Lactobacillus johnsonii La1 (La1) were examined in aged mice and aged mice with PEM. Twenty-month-old male 57BL6/n mice (n = 28) were divided into four groups and received the following diet for 14 d: a complete diet (20% protein) without Lal (control) or with Lal or a low-protein diet (5% protein) to induce PEM, with or without La1. All mice were immunized with diphtheria toxin (DT) with alfacalciferol at 7 d and sacrificed 14 d after starting the experimental diets. RESULTS: Serum albumin concentrations and body weight, both of which were reduced by the low-protein diet, were ameliorated by La1 intake and were the same as in mice receiving the control diet. Anti-DT immunoglobulin (Ig) A in fecal extract was increased by La1 intake in mice receiving the complete and low-protein diets. Serum anti-DT IgA, IgG, splenocyte proliferation, and CD8(+) T cells were reduced by the low-protein diet and restored by La1 intake. CONCLUSION: La1 enhances intestinal IgA production and helps recover nutritional status and systemic immune responses in aged mice with PEM. It is possible that La1 may contribute to immune system recovery in immunocompromised hosts such as elderly humans with PEM.


Subject(s)
Immunity, Mucosal/drug effects , Lactobacillus/physiology , Probiotics/administration & dosage , Protein-Energy Malnutrition/immunology , Serum Albumin/analysis , Aging/blood , Aging/physiology , Analysis of Variance , Animals , Dietary Proteins/administration & dosage , Feces , Immunoglobulin A/blood , Immunoglobulin A/immunology , Lactobacillus/growth & development , Lactobacillus/immunology , Male , Mice , Mice, Inbred C57BL , Nutritional Status , Protein-Energy Malnutrition/blood , Random Allocation
11.
Life Sci ; 79(11): 1056-61, 2006 Aug 08.
Article in English | MEDLINE | ID: mdl-16650442

ABSTRACT

OBJECTIVE: It is known that immune functions are altered in various ways by obesity. However, changes in the intestinal immune system resulting from obesity remain poorly understood. Oral tolerance is a system that suppresses antigen specific immune responses to orally administrated antigens. The intestinal immune system is intimately associated with the oral tolerance system, that acts to prevent allergic and inflammatory diseases. In this study we investigated the effect of obesity on induction of oral tolerance to ovalbumin (OVA) in an animal model of obesity. RESEARCH METHODS AND PROCEDURES: Obese mice induced by a high fat diet and control mice were allowed free access for 3 days to a 1%-ovalbumin (OVA) solution in drinking water. After continuous feeding of the antigen, all the mice were immunized by two intraperitoneal injections of OVA administered 7 days apart. RESULTS: In the control mice, induction of oral tolerance caused an increase in antigen specific IgG1 levels and a decrease in IgG2a levels. In contrast, the IgG1/IgG2a ratio was reversed in obese mice. OVA-specific IL-2 production was suppressed by antigen feeding in both the control and obese mice; however, suppression of OVA-specific IL-10 was observed only in the control mice. Although OVA-specific IgA and IgM were not affected by antigen feeding, the obese groups of mice had significantly lower titers of antibodies. DISCUSSION: These findings suggest that obesity may affect induction of oral tolerance following antigen feeding and that these changes may be related to the inflammatory reaction.


Subject(s)
Immune Tolerance , Mouth/immunology , Obesity/immunology , Animals , Antigens/administration & dosage , Antigens/immunology , Diet , Dietary Fats/toxicity , Immunoglobulin A/blood , Immunoglobulin G/blood , Immunoglobulin M/blood , Interleukin-10/metabolism , Interleukin-2/metabolism , Interleukin-4/metabolism , Mice , Obesity/chemically induced , Ovalbumin/administration & dosage , Ovalbumin/immunology , Spleen/cytology , Spleen/immunology
12.
Int Arch Allergy Immunol ; 133(1): 19-28, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14646375

ABSTRACT

BACKGROUND: Estrogen plays an important modulatory role in the immune system, and is concerned with the pathophysiology of autoimmune diseases such as rheumatoid arthritis (RA), although the mechanism has not yet been clarified. Oral tolerance, a form of specific peripheral tolerance, which is recognized as a new therapeutic strategy, is related to the function of gut-associated lymphoid tissue. METHODS: In this study, using collagen-induced arthritis as an animal model of RA, the effects of 17beta-estradiol (E2) on oral tolerance induction were investigated. For induction of oral tolerance, mice were fed 60 microg type II collagen (CII) for 10 consecutive days prior to each CII immunization. Mice in the E2 treatment groups were injected with 5 microg (low dose) or 500 microg (high dose) E2 three times during the induction of oral tolerance. RESULTS: Oral tolerance induction suppressed the occurrence of arthritis, the proliferative response of splenocytes to CII and the specific DTH response. However, E2 treatment abrogated the suppression, which might be connected with a change in function of Peyer's patch (PP) lymphocytes. CONCLUSION: These results suggest that oral tolerance induction might be affected by estrogen treatment through alteration of intestinal immune responses.


Subject(s)
Arthritis, Experimental/immunology , Arthritis, Rheumatoid/immunology , Estradiol/immunology , Hypersensitivity, Delayed/immunology , Immune Tolerance/immunology , Animals , Apoptosis/immunology , Arthritis, Experimental/pathology , Arthritis, Rheumatoid/pathology , Cell Division/immunology , Estradiol/blood , Formazans , Immunoglobulin G/immunology , Immunohistochemistry , In Situ Nick-End Labeling , Lymphocytes/cytology , Lymphocytes/immunology , Male , Mice , Mice, Inbred DBA , Peyer's Patches/immunology , Tetrazolium Salts
13.
Metabolism ; 51(10): 1241-6, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12370841

ABSTRACT

Some epidemiologic surveys have demonstrated that asthma is more prevalent in obese children and adults. However, the mechanism of association between obesity and asthma has not been fully clarified. This report investigates a murine model for antigen-induced asthma and diet-induced obesity from an immunologic perspective. For the induction of obesity, C57BL/6J mice were fed a high-fat diet supplemented with lard or soybean oil. Mice were then sensitized and challenged with ovalbumin (OVA) to induce allergic lung inflammation. OVA-specific serum immunoglobulin levels were lower in obese mice compared with non-obese control mice. The decline of OVA-specific IgE in the soybean oil group was found to be especially pronounced. However, obese mice with OVA-induced asthma showed a higher sensitivity of antigen-induced T-cell responses, and increased gamma interferon (IFN-gamma) production of splenocytes with phytohemagglutinin (PHA) stimulation. Furthermore, mast cell numbers in the tracheal mucosa were increased in obese mice upon sensitization by OVA. These results suggest that obesity-induced changes in T-cell function may be partly involved in the pathophysiology of asthma in human obesity, rather than Ig E-mediated allergic responses.


Subject(s)
Asthma/immunology , Diet , Obesity/immunology , Ovalbumin/immunology , Adipose Tissue/anatomy & histology , Adipose Tissue/growth & development , Animals , Body Weight/physiology , Cell Division/drug effects , Dietary Fats/pharmacology , Energy Metabolism/physiology , Immunoglobulins/biosynthesis , Interferon-gamma/biosynthesis , Interleukin-2/biosynthesis , Leptin/blood , Mice , Mice, Inbred C57BL , Mitogens/pharmacology , Respiratory Hypersensitivity/immunology , Spleen/cytology , Spleen/immunology
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