Color and chemical properties of oil used for deep frying on a large scale.

Acid value (AV), polar compound content (PC), carbonyl value (CV) and Gardner color of oil used for deep-frying in kitchens at a supermarket, lunch chain store, restaurant, eating house, and hospital were analyzed. All AVs obtained but one (3.38) were within the limit set by the Food Sanitation Act of Japan (AV ≤ 3, peroxide value ≤ 30). However, some oil samples had a PC over 25%, which is beyond the limit legislated by some European countries. When the relation between the Gardner color and the AV, PC, or CV of the oil was investigated, well correlated logarithmic regression curves were obtained from the oil of all kitchens except the hospital kitchen. However, the use of lard-containing canola oil without oil replenishment in the eating house increased color values rapidly. All of the values obtained from pure vegetable oil used almost daily were plotted on a graph. It was found that kitchen-by-kitchen differences in fryer, vegetable oil, frying temperature, heating time, and amounts and kinds of foods fried did not influence the relation between Gardner color value versus AV, PC or CV. In conclusion, frying vegetable oil used in large-scale kitchens without official inspection can be better controlled with Gardner color determination by the operators and administrators. This would improve the quality of the oil ingested by facility patrons.

Oxidation of frying oils during intermittent usage.

We reported previously that in oils used for frying by commercial establishments, a high correlation was observed among their Gardner colors, polar compound contents (PC), carbonyl values (CV) and acid values (AV). However, this was not true for frying oils used in hospitals. In the present study, oils that had been used for deep-frying in hospital kitchens were collected and assayed for PC, CV, AV, and Gardner color value to determine the reason for the differences from oil used in commercial establishments. Hospitals were selected so that variation in the number of inpatients, frying oil fatty acid composition, and frying frequency was obtained. As previously observed, we did not find good correlations between the color of the frying oil and the PC, CV or AV, respectively. The extent of oxidation in batches of oil repeatedly used for deep-frying was in the following order: soybean oil > blended oil > canola oil. After use in deep-frying, where the oxygen content goes effectively to zero, allowing the oil to stand at room temperature resulted in the quick and steady absorption of oxygen until it returned to its initial content. In addition to the effect of thermal treatment of oil, standing time between usages is a significantt cause of oxidation.

Ferulic acid esters and weight-loss promoting effects in rats.

We previously fed rats with an ester (90 ppm in a powdered AIN93G diet) synthesized from gallic acid and 1,2-dioleoyl glycerol and found that it promoted weight loss more effectively than either octyl gallate or gallic acid. Here, we esterified ferulic acid (FerA) with oleic acid, monooleoyl glycerol and dioleoyl glycerol to obtain oleoyl ferulic acid (FO), feruloyl monooleoyl glycerol (FMO) and feruloyl dioleoyl glycerol (FDO) esters, respectively. A mixture of AIN93G and 90 ppm of each ester and FerA was fed to 10-week-old male Wistar rats for 12 weeks. The FMO and FDO groups weighed less than the control group starting from approximately 16 weeks of age. At 21 and 22 weeks of age, weight significantly differed between the FMO and both groups, respectively, and controls. The FO, FerA and control groups did not significantly differ in terms of body, liver, kidney and retroperitoneal fat tissue weights and serum biochemical findings. We concluded that the hydroxyl group of FerA is essential for promoting weight loss and that the carboxyl group should be esterified with alcohol. In addition, monooleoyl glycerol and dioleoyl glycerol did not show any difference as the alcohol moiety of the ester in the weight loss effect.

Gallic acid glycerol ester promotes weight-loss in rats.

Lifestyle-related diseases arise from obesity in 30 - 60% of cases. In recent years, food functions controlling the nutritional physiology of lipids have been a focus of disease prevention. Animal feeding experiments have revealed that esters made from gallic acid (GA) and (-)-epigallo-catechin (EGC) or linoleyl alcohol are more effective in weight-loss promotion and metabolic syndrome management than are intact GA and EGC. In this study, an ester (DOGGA) was chemically synthesized from GA and 1,2-dioleoyl glycerol and its effect was compared to that of octyl gallate (OG) and GA in male Wistar rats fed a powdered standard diet containing 7% frying oil for 12 weeks. Results revealed remarkably low body weight gains and food efficiency ratios in the DOGGA group, and the effects of OG were less pronounced than those of DOGGA. The GA group showed no difference from the control group. In addition, fecal lipid content in the DOGGA group was statistically higher than that in the control group, although organ weights and serum biochemical analyses did not differ between the groups. In conclusion, the data suggested that DOGGA promoted weight-loss more effectively than OG and GA did and that the alcohol moiety of gallate is not necessarily EGC and linoleyl alcohol.

Effects of oil thermally processed with vegetable protein on gastrointestinal tract content transfer.

It has been reported that oil heated with vegetable protein under reduced pressure, followed by filtration (soy oil), decreased body, liver and retroperitoneal fat tissue weights and serum triacylglycerol levels in Wistar rats. In order to clarify the mechanism of these weight-loss promoting effects, gastrointestinal tract content transfer was traced. Fasted 10-week-old rats were fed a slurry containing AIN93G without fat, Cr(2)O(3) (marker), and 7 wt% soy oil or fresh oil (control) and sacrificed at 20, 60, 120, or 360 min; then, blood, stomach, small intestine, cecum, colon and feces were collected. The results indicated that the content transferred faster from stomach to small intestine in the soy oil group than in the control group. At 60 min after the ingestion of diet, an increased serum triacylglycerol level was found in the soy oil group. In addition, fecal excretion in the soy oil group was significantly higher 120 min after the administration than in the control group, suggesting that soy oil stimulated peristalsis of the colon and that colon contents (food ingested before administration) were actively excreted.

The mechanism of weight-loss promoting effects of oil heated with vegetable protein.

We have previously reported that a soy oil-containing experimental diet (fat-free AIN93G containing oil thermally processed with soybean protein followed by filtration), inhibited body weight increases without any adverse effects when given ad libitum to male Wistar rats for 12 weeks. In the present paper, the mechanism of weight-loss promoting effects was investigated. Fasted 10-week-old rats were fed a slurry composed of AIN93G (fat-free), Cr(2)O(3) (marker), water, and 7 wt% soy oil or fresh oil (control) and sacrificed at 20, 60, 90, 120, 150, 210, 270 or 360 min. The stomach, small intestine, cecum, colon and feces were then collected to determine the distribution of the slurry in the digestive tract. The results indicated that the content was transferred faster from stomach to small intestine in the soy oil group than in the control group. Fecal excretion (derived from a commercial standard diet ingested before slurry administration) in the soy oil group was significantly higher than in the control group. Digestive enzyme activities, lipase, sucrose, and maltose, were not inhibited by soy oil. In addition, feces collected in the 12-week feeding experiment were more in the dry weight and contained higher levels of nitrogen and water in the soy oil group than in the control group, revealing that an increased amount of nutrition was continuously excreted in the former group. The above-described findings suggest that soy oil stimulated peristalsis of the gastrointestinal tract and that colon contents are actively excreted, resulting in safe and steady body weight decreases.

A novel body weight-loss promoting oil prepared with vegetable protein.

It has been reported that oil thermally processed with wheat gluten (gluten oil) exhibited safe weight-loss promoting effects in animal experiments. However, as the oil has a high color index, and its chemical properties and smell differ from those of fresh oil, it is uncertain if the oil will find market acceptance. In order to resolve the issue, frying oil was heated with soybean protein under reduced pressure (soybean protein oil), resulting in a product with an appearance, chemical properties and smell comparable to those of fresh oil. This improved oil was mixed (7 wt%) with powdered AIN93G no fat, defined standard diet and fed to 10-week-old Wistar rats ad libitum. The experimental rats grew normally, ingesting the same amount as that of the control rats; however, there was a negative correlation between body weight increases and fecal weight increases. After the 12-week feeding period, all the rats were sacrificed to obtain blood and organs. In the experimental group, liver weight, retroperitoneal fat tissue weight and serum triacylglycerol (TG) levels decreased significantly. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and histological analysis supported the safety of the improved oil. In conclusion, it was found that soybean protein oil inhibited body weight increases without any adverse effects in animal experiments. The oil holds promise as a novel dieting oil that steadily decreases body weight at an appropriate rate.

Oil in a commercial standard diet needs its product specifications.

As our survey found that some commercial standard diets for laboratory animals contained oil with chemical properties of highly deteriorated oil, their influence should be checked on animals especially of very young age. Three-week old weanling Wistar rats were fed a commercial standard diet (commercial standard diet group) or AIN93G (AIN93G group), defined diet, for 7 weeks. Then both groups were fed AIN93G for 12 weeks. As a result, all the rats grew normally without diarrhea, seborrhea, dermatitis, or excessive hair loss through the feeding period and there was no significant difference in body weight increase, feed ingestion amounts and organ weights. But fecal excretion was high at 10 weeks of age when the diet was switched from the commercial standard diet to AIN93G. Although serum aspartate aminotransferase (AST) and alanin aminotransferase (ALT) of the commercial standard diet group were not statistically higher than those of the AIN93G group, two rats out of 8 in the former group showed dark-red patches on the liver surface, and necrosis in histological analysis. In addition, slight fatty degeneration of all the liver, and swelling tubuler epithelium of kidneys were also found in the group. Serum levels of triacylglycerol (TG), glucose (GLC) and total cholesterol (T-CHO) were high, and free fatty acids (NEFA), low in the commercial standard diet group in good accordance with our previous result from the study on ingestion of deteriorated oil. In conclusion, product specifications of oil in commercial standard diets should be laid down to pursue a reliable animal experimentation.

Role of vegetable protein in the preparation of weight loss-promoting oil.

We have reported that oil thermally processed with protein promoted safe and steady weight loss in animal experiments. In the present study, an oil for use in weight control was prepared by heating fresh oil with wheat gluten or soybean protein to determine the influence of protein differences on the weight loss-promotion effect. The 2 kinds of oil obtained, which differed neither from commercial fresh oil (starting oil) nor from one another in appearance, chemical properties, and aroma, were mixed (7%) with powdered AIN93G no-fat, defined standard diet and fed to 10-week-old Wistar rats ad libitum. After a 12-week feeding period, the rats were sacrificed to obtain blood and organs. There were no differences in amounts ingested, body weight increases, fecal excretion, organ weights, serum biochemical analyses, contents and fatty acid compositions of lipids of retroperitoneal fat tissue, or organ observations. Aspartate aminotransferase (AST), alanine aminotransferase (AST), and histological analysis supported the safety of the oil. In conclusion, the differences between wheat gluten and soybean protein in amino acid composition, both of the proteins and as free amino acids, were unrelated to the weight loss-promoting effect of the oil. Minor components in the vegetable proteins may have contributed to the effect on body weight.

Effects of oil heated with gluten on weight-loss dieting. II.

We previously proposed that oil heated with gluten was suitable for use as a safe oil for weight-loss dieting. In the present paper, the properties of the oil were improved, and the weight-loss effect was compared with that of heated oil. Fresh oil was heated for 10 h at 180 degrees C with or without gluten and filtered using filter paper. A powdered diet (AIN93G; no fat) was mixed with 7 wt% of fresh oil (control) or filtrates of the heated oils described above, and the mixture was fed to male Wistar rats for 12 weeks. The gluten and heated oil groups showed no gross symptoms attributable to the experimental oils but had a slowed body weight increase; a significant difference was found in weight on and after 21 weeks of age as compared to rats consuming the control diet, and fecal excretion was increased as compared to the control group. Serum levels of triacylglycerol, phospholipids, cholesterol, and glucose of the gluten and heated oil groups were significantly lower than those of the control group. High aspartate aminotransferase (AST) levels occurred more frequently in the heated oil group than the gluten group. The number of rats with dark red patches on the surface of the liver, which are indicative of liver damage, was higher in the heated oil group. In conclusion, the weight-reducing effect of the oil heated with gluten was confirmed and improved by removing traces of heated gluten from the oil.