../Verlag%20Hans%20Huber

International Journal for Vitamin and Nutrition Research, 1/1997


The Effect of Retinol and Retinoic Acids on Lipoxygenase Activity

Dafna Goldreich1, Shlomo Grossman1, Yossi Sofer1, Eyal Breitbart1 and David Sklan2

1 Department of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel
2 Department of Animal Sciences, Faculty of Agriculture, Hebrew University, Rehovot 76100, Israel

Summary

Lipoxygenase catalyzes the dioxygenation of polyenoic fatty acids such as linoleate and arachidonate. The aim of the present study was to examine the effect of retinol, all-trans-retinoic acid and 13-cis-retinoic acid on the activity of lipoxygenase-1 and lipoxygenase-2 towards linoleic acid.
Lipoxygenase activity toward linoleic acid was followed by determining changes in absorption at 234 nm. All retinoids inhibited lipoxygenase-1 and lipoxygenase-2 activity. Lipoxygenase-2 activity towards linoleic acid was rapid at pH 6.5; all-trans-retinol (10 mM) caused a 50% inhibition in reaction rate. All-trans-retinol was oxidized in parallel with diene production by lipoxygenase-2. Lipoxygenase-2 activity on linoleic acid was competitively inhibited by all-trans-retinol and all-trans-retinoic acid; 13-cis-retinoic acid exhibited mixed type inhibition. Activity of lipoxygenase-1 towards linoleic acid at pH 9.0 was also inhibited by retinoic acids by 32-73%. All-trans-retinoic acid and 13-cis-retinoic acid inhibited lipoxygenase-1 activity competitively, whereas all-trans-retinol inhibited lipoxygenase-1 activity in a mixed manner.
These findings suggest that retinoids may bind to the active site of the enzyme or simultaneously act as an antioxidant.

Keywords

Vitamin A - Lipoxygenase - Soya - Retinol - Retinoids

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern

Back - IJVNR Home


Influence of Ascorbic Acid on the Response to Mitogens and Interleukin Production of Porcine Lymphocytes

Joseph Schwager and Jürgen Schulze

Centre de Recherche en Nutrition Animale, Société Chimique Roche, 68305 Village-Neuf, France

Summary

The influence of ascorbic acid (AA) on lymphocyte functions was examined in vitro and ex vivo in peripheral blood mononuclear cells (PBMC) of vitamin C-deficient pigs, which are unable to synthesise ascorbic acid. AA is accumulated to physiological levels in PBMC in vitro. The cell proliferation induced by T lymphocyte mitogens was unaltered at all AA concentrations tested (0-400 mg/ml, i.e. 0-2.3 mM). Conversely, the response to pokeweed mitogen (PWM) which activates T and B lymphocytes was significantly reduced with increasing intracellular and extracellular AA concentrations. The response to lipopolysaccharide (LPS) showed a tendency to increase at low (9 mM) and was significantly reduced at high AA concentrations (>36 mM). The IL2 production induced by PWM (but not by concanavalin A (Con A) or phytohemagglutinin (PHA)) decreased at high AA (>142 mM). In contrast, IL6 production induced by mitogens was not dependent on AA concentrations. In concordance with these results, AA-depleted PBMC which were obtained from pigs that were fed an AA-free diet, displayed an increasing response to LPS and PWM. Collectively, the data indicate that ascorbic acid selectively influences the proliferation of B lymphocytes and negatively acts on IL2 production by T lymphocytes when a threshold of saturation is exceeded.

Keywords

Vitamin C - Immune function - Interleukins - Lymphocyte proliferation - Swine

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern

Back - IJVNR Home


Effect of Vitamin B12-Deficiency on Testicular Tissue in Rats Fed by Pair-Feeding

Tetsunori Kawata1, Akiko Tamiki1, Ayako Tashiro1, Kyoko Suga1, Sachiko Kamioka1, Kazuhiro Yamada2, Masahiro Wada3, Nobuo Tanaka4, Tadahiro Tadokoro2 and Akio Maekawa2

1 Faculty of Education, Okayama University, Tsushimanaka, Okayama 700, Japan
2 Department of Agricultural Chemistry, Faculty of Agriculture, Tokyo University of Agriculture, Setagaya-ku, Tokyo 156, Japan
3 Department of Nutrition, Faculty of Agriculture, Tokyo, University of Agriculture, Setagaya-ku, Tokyo 156, Japan
4 Department of Internal Medicine, The Jikei University of Medicine, Ktsushika-ku, Tokyo 124, Japan

Summary

The effect of vitamin B12 (B12)-deficiency on testicular tissue was investigated through morphological observations of the rats which had been fed on a B12-deficient soybean protein diet by pair-feeding for 100 days. Testicular B12 content was depressed distinctly by the deficiency. Testes weight and their relative weight (weight per 100 g body weight) as well, decreased significantly as compared with those of pair-feeding control rats. Although the decrease in the testicular B12 content due to B12-deficiency was compensated by the administration of cyanocobalamin (CN-B12), alleviation of the decrease in testes weight and relative testes weight was not observed under the condition of the short-term CN-B12 administration. Morphological observations of the testicular tissue in B12-deficient rats revealed atrophy of the seminiferous tubules and aplasia of sperms and spermatids, while testicular findings in both ad libitum-feeding control rats and pair-feeding control rats were normal. There was a tendency for the decrease in seminiferous tubules showing spermatogenesis to be alleviated by administration of CN-B12. The above results indicate that the morphological changes in the testicular tissue are ascribable to B12-deficiency.

Keywords

Vitamin B12 -deficiency - Pair-feeding - Testicular morphology

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern

Back - IJVNR Home


Zinc Status in Vitamin B6 Deficiency

D. Pillay1, P. Gathiram1 and J.B. Ubbink2

1 Department of Human Physiology and Physiological Chemistry, University of Durban-Westville, Private Bag X54001, Durban, 4000, South Africa
2 Department of Chemical Pathology, University of Pretoria, P.O. Box 2034, Pretoria 0001, South Africa

Summary

Three groups of young male Wistar rats were maintained on diets consisting of 7 mg pyridoxine hydrochloride/kg diet (control and pair-fed groups) and 0 mg pyridoxine hydrochloride/kg diet (deficient group) for six weeks. The zinc status of all rats was assessed by measuring their erythrocyte zinc-metallothionein-1 (Zn-Mt-1) and plasma zinc levels. A significant difference (p < 0.001) in plasma zinc levels was observed between the deficient group and the control and pair-fed groups (1.35 mg/ml ± 0.08, 1.99 mg/ml ± 0.06 and 2.03 mg/ml ± 0.07 respectively). Erythrocyte Zn-Mt-1 levels were significantly lower in vitamin B6 deficient rats when compared to control animals. No significant difference in Zn-Mt-1 levels existed between vitamin B6 deficient and pair-fed groups suggesting that the reduced Zn-Mt-1 levels in vitamin B6 deficient rats may be due entirely to their decreased food intake (8.9 g/day compared to 15 g/day of control rats).

Keywords

Vitamin B6 - Zinc - Metallothionein - Status

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern

Back - IJVNR Home


Plasma Selenium in Healthy Man Before and After Nutratherapy

Jan Karlsson1, Gillis Lundgren2 and Ragnhild Rønneberg3

1 OBLA AB, Vaxholm, Sweden
2 Analytica AB, Näsby Parks Företagspark, Stockholm, Sweden
3 Pronova Biocare as, Lysaker, Norway

Summary

Females (n=28) and males (n=39) had their plasma analysed for selenium (Se), ubiquinone, a-tocopherol (vitamin E), the essential fatty acid (EFA) classes: omega-3 (w-3, n-3) and omega-6 (w-6, n-6) fatty acids. Selenium averaged 0.99±0.03 mmol/l and was positively related to plasma ubiquinone, a-tocopherol and the EFA index: the w-6/w-3 ratio. Food supplements (nutratherapy) with the lipophilic antioxidants ubiquinone and a-tocopherol (Q+E) had no effect on selenium but the addition of omega-3 fatty acids as a fish oil concentrate (Q+E+n-3) had (1.12±0.05 mmol/l, + 36%, p <0.001). (Q+E) and (Q+E+n-3) with the addition of selenium (200 mg or 2.5 mmol a day) raised selenium but not higher than (Q+E+n-3) itself (1.17±0.12 mmol/l, p <0.05). After (Q+E) alone, selenium was related as at base-line to both ubiquinone and a-tocopherol but not to any marker for EFA. After (Q+E+n-3), selenium was only related to ubiquinone. An unsatisfactory a-tocopherol nutratherapy was suggested as the explanation. EFA or markers for EFA were in no situation related to plasma selenium.

Keywords

Plasma selenium - Se - Antioxidant vitamins - Essential fatty acids - Ubiquinone - a-Tocopherol - Vitamin E - Omega-3 fatty acids - n-3 - Omega-6 fatty acids - n-6

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern

Back - IJVNR Home


The Vitamin Status of Young British Adults

David Benton1, Jürg Haller2 and Joyce Fordy1

1 Department of Psychology, University College Swansea, Swansea, Wales, U.K.
2 Department of Clinical Nutrition, Hoffmann-La Roche, Basel, Switzerland

Summary

Using biochemical indices thiamin, riboflavin, pyridoxine, ascorbic acid, retinol, a-tocopherol, folic acid, cyanocobalamin, carotene and biotin status were assessed in a sample of 243 young British adults. Using conventional definitions the number of individuals whose vitamin status can be described as adequate, marginal or deficient was determined. Vitamin status was related to alcohol intake and smoking. The status of ascorbic acid, cyanocobalamin, a-tocopherol, folic acid, and in males retinol, was adequate in the majority of cases. In the cases of riboflavin and pyridoxine the status of a substantial minority was either borderline or deficient. The thiamin and biotin status of a minority of both sexes, and retinol in the females, was marginal. In males alcohol was associated with better retinol, ascorbic acid, a-tocopherol and pyridoxine status and lower levels of biotin. Lower carotene values were associated with drinking alcohol. In both sexes those who smoked had lower ascorbic acid, folic acid and carotene values. In males smoking was additionally associated with lower riboflavin and biotin; in females cyanocobalamin and a-tocopherol were lower. As all the subjects were students volunteers, care should be taken in generalizing the data to other groups.

Keywords

Ascorbic acid - Biotin - Carotene - Cyanocobalamin - Folic acid - Pyridoxine - Retinol - Riboflavin - Thiamin - a-Tocopherol - Vitamin status

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern

Back - IJVNR Home


Food Intake and Body Mass Index in the Privately Institutionalized Elderly in Tehran

Mahshid Ahrari and Masood Kimiagar

Department of Human Nutrition, National Nutrition Institute, P.O. Box 19395/4741, Tehran, I.R., Iran

Summary

Food intake and Body Mass Index (BMI) of privately institutionalized elderly in Tehran was studied using a 5-day food intake survey and anthropometric measurements. Thirty-seven males and sixty-three females in private institutions were selected. The intake of many nutrients including protein, calcium, zinc, vitamins A, riboflavin, folic acid and cobalamin, were deficient. Almost half the subjects were under the 5th percentile of standard BMI for their age and sex, indicating chronic energy malnutrition. More attention needs to be paid to this group of vulnerable people.

Keywords

Nutritional status - Institutionalized elderly - Malnutrition

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern

Back - IJVNR Home


Determination of Carotenoids in Vegetable Foods and Plasma

P. Riso and M. Porrini

Dipartimento di Scienze e Tecnologie Alimentari e Microbiologiche, sez. Nutrizione, Università degli Studi di Milano, Via Celoria 2, 20133 Milano, Italy

Summary

In this paper a HPLC method for the determination of lutein, zeaxanthin, b-cryptoxanthin, a-carotene, b-carotene and lycopene in mixed vegetables and fruit and in human plasma is described.
The carotenoids were well separated and the separation was achieved within fifteen minutes using a HPLC system consisting of a 5µm Vydac 201TP54 C18 column, an UV detector, methanol-tetrahydrofuran (95:5 v/v) as mobile phase and a flow rate of 1.0 ml/min. The validity of the separation method was determined by evaluating the linearity of the calibration graphs of each carotenoid (between 0.1 and 1.0 µg/ml for all compounds except lycopene between 0.1 and 0.8 µg/ml, r = 0.999) and the accuracy of the chromatographic response (CV <10%). The reproducibility of the retention times was also good.
In the foods samples the extraction procedure was very effective whereas, the saponification step significantly damaged some of the carotenoids. In the plasma the extraction and separation of these compounds were also effective and the qualitative data obtained comparable with those reported in literature. The use of echinenone as internal standard helped to improve quality control.

Keywords

Carotenoids - Vegetable foods - Plasma - Extraction - HPLC

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern

Back - IJVNR Home


The Alginate Reduce the Postprandial Glycaemic Response by Forming a Gel with Dietary Calcium in the Stomach of the Rat

Atsutane Ohta1, Azusa Taguchi1, Toshio Takizawa1, Takashi Adachi1, Shuichi Kimura2 and Naotaka Hashizume3

1 Nutritional Science Center, Biscience Laboratories, Meiji Seika Kaisha, Ltd., Saitama 350-02, Japan
2 Professor Emeritus at Tohoku University, Miyagi 981, Japan
3 Professor at Department of Laboratory medicine, Ohashi hospital, Toho University School of Medicine, Meguro-ku, Tokyo 153, Japan

Summary

Soluble dietary fibers include an alginate which reduces the postprandial glycaemic response. We speculated that the cause of the reduction of alginate on the glycaemic response is the gel formation of alginate with dietary calcium in the stomach. The aim of the present study was to confirm our hypothesis and to examine the effect of the sugar composition of alginates on the glycaemic response and the effect of continuous feeding of alginate-containing diet to rats. Diabetic rats were made by injecting streptozotocin (STZ) intravenously. These rats were fed 5 g of the experimental diet with or without sodium alginate and with or without calcium after overnight fasting. In the rats fed the diet containing both alginate and calcium, the postprandial glycaemic response was lower than in the rats fed other diets and gastric contents were retained as gel form. Three b-d-mannuronic acid (M) to a-l-guluronic acid (G) (ratios (M/G 0.5, 1.3, 2.1) of alginates were not associated with the acute glycaemic response in STZ rats. Then, we fed normal rats with an alginate-free or one of three respective alginate-containing diets for 4 weeks. During the first 2 weeks of the feeding period, the total amount of food intake of rats fed the G-rich alginate diet was smaller than that of rats in the other dietary groups. Moreover, the weight of the dorsal abdominal adipose tissue of rats given the G-rich alginate diet was the lowest among the dietary groups.
We conclude that the reductive effect of alginate feeding on the postprandial glycaemic response was not caused only by their inherent viscosity, but also by gel formation with dietary calcium in the stomach. Moreover, it is necessary to pay attention to the M/G ratio of alginates for estimating their physiological effect.

Keywords

Alginate - Calcium - Gel formation - Gastric emptying - Glycaemic response

International Journal for Vitamin and Nutrition Research, 1997, Heft 1 © Verlag Hans Huber, Bern


wwwadmin@hanshuber.com, 26. Juni 1997