Archives for: January 2009
STUDY: Vitamin-rich foods, not supplements, appear best
JOURNAL: Journal of the American Medical Association
AUTHORS: Martha Clare Morris
ABSTRACT: In the latest work to show that vitamins may protect against dementia, new studies suggest that eating nuts, leafy green vegetables and other foods rich in antioxidants such as vitamin E may reduce the risk of Alzheimer’s.
COMMENTARY: The connection, at least, is considered plausible: Antioxidant vitamins have been shown to block the effects of oxygen molecules called free radicals, which can damage cells and are thought to contribute to cancer and heart disease. And lesions typically associated with exposure to free radicals have been found in the brains of Alzheimer’s patients.
One of the studies found strong effects from vitamins E and C. In the other, results from vitamin E foods were more conclusive.
There was no protective effect in participants with a gene variation called apoplipoprotein E-4, which has been linked to the development of Alzheimer’s.
Other work has hinted that high levels of the amino acid known as homocysteine may also be associated with Alzheimer’s disease, suggesting that folic acid and other B vitamins may offer some protection.
There’s no question, experts say, that folic acid and B vitamins break down homocysteine in the body, thereby reducing blood levels. But the link between homocysteine and dementia still needs to be confirmed.
STUDY: Plant-based, edible compounds are one answer
JOURNAL: Diabetes Week
AUTHORS: Sam J. Bhathena
ABSTRACT: Obesity and diabetes mellitus are two nutritional disorders that have become major public health concerns in industrialized countries because of their epidemic proportions and association with major cardiovascular risk factors that are responsible for excess morbidity and mortality. Researchers are looking for ways to combat these diseases.
COMMENTARY: Phytoestrogens are a group of biologically active plant-based compounds.
Phytoestrogens are present in edible plants that can be classified as isoflavones, lignans and coumestaus. Soybean is an abundant source of isoflavones in the human diet, while flaxseed is the richest source of lignans.
Earlier studies in obese animals and humans have suggested that soy, as a source of dietary protein, has significant antiobesity effects.
A study conducted in genetically obese mice found that soy protein and its hydrolsate were more effective than whey protein in weight reduction. This effect may be due to an active tetrapeptide present in soy. Several studies reported increased insulin sensitivity in rats fed isolated soy proteins compared with rats fed casein. A 37-kDa protein in soy appears to modulate insulin action on fat decomposition. Studies on the role of flaxseed and its components in obesity and diabetes in humans are limited.
Lean and obese rats were fed diets containing either 20% casein or 20% isolated soybean protein or 20% flaxseed meal for 26 weeks. The lean rats were hypertensive while the obese rats showed symptoms of type II diabetes. Obese rats had significantly higher levels of plasma glucose, triglycerides, total cholesterol, (high-density lipoprotein cholesterol [HDL-C] and low-density lipoprotein cholesterol [LDL-C]).
Soybean significantly decreased total cholesterol and LDL in both lean and obese rats but had no significant effect on glucose.
Flaxseed decreased total cholesterol and triglycerids in both lean and obese rats, but it significantly decreased HDL-C and LDL-C only in obese rats. Flaxseed also decreased glucose in lean but not in obese rats and it had greater effect on various parameters than did soybean.
Soybean and flaxseed affected plasma lipids and a number of enzymes. They also had varying effects on tissue weights in lean and obese rats. Obese rats compared with lean rats had significantly lower plasma creatinine but higher total bilirubin, blood urea nitrogen, alanine aminotransferase and lactate dehydrogenase.
Both soy and flaxseed meal decreased total bilirubin, protein and uric acid in the lean rats, but the effects in obese rats were mixed.