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Who says we have to suffer...to live a healthy happy vibrant life?

Red wine and dark chocolate... might seem decadent...but these guilty pleasures also might help us live longer...and healthier lives. Red wine and dark chocolate definitely improve an evening..but they also contain resveratrol..which lowers blood sugar. Red wine is a great source of catechins..which boost protective HDL cholesterol. Green tea? Protects your brain..helps you live longer..and soothes your spirit.

Food for Thought, the blog, is about living the good life...a life we create with our thoughts and our choices...and having fun the whole while!

I say lets make the thoughts good ones..and let the choices be healthy...exciting...and delicious! Bon Appetit!

Showing posts with label Brain Health. Show all posts
Showing posts with label Brain Health. Show all posts

Thursday, May 31, 2018

Is vitamin C deficiency related to decreased cognitive function? It may be!





There are numerous causes and consequences of Vitamin C deficiency in the brain. 

Several risk factors for Vitamin C deficiency have been identified, including disease, smoking, and inadequate dietary intake, but also pregnancy and genetics have been shown to affect Vitamin C levels. Based on Vitamin C’s involvement in important processes in the brain, there is reason to believe that these could be adversely affected by a deficiency. The functions of Vitamin C include its antioxidant function of upholding redox balance, and thus reducing the effects of oxidative stress in the brain. But vitamin C also has other important functions in the brain. These include modulation of the cholinergic, catecholinergic, and glutamergic systems of the brain. Vitamin C supports the general development of neurons ( nerve cells in the brain) through maturation, differentiation and myelin formation. Vitamin C is involved in several processes in the vascular system including helping maintain integrity and function of blood vessels, e.g., nitric oxide synthase, which regulates vessel relaxation through production of nitric oxide. 

Abbreviations: NOS, nitric oxide synthase; ROS, reactive oxygen species; NMDA, N-methyl-d-aspartate.

Vitamin C deficiency appears to pose numerous threats to cognitive function. The involvement of vitamin C in vessel integrity, antioxidant balance and neuromodulation in the brain has prompted investigations into the effect of the vitamin on the developing brain, in aging and in stroke. In the developing brain, neuronal density and maturation is compromised by Vitamin C deficiency, giving rise to decreased brain volume. In the aging brain deficiency affects ACh release and may impair cognitive function through reduced signal transduction but also through amyloid β deposition resulting in generation of reactive oxygen species and increased neuronal impairment in people suffering from Alzheimer’s disease. In stroke, Vitamin C deficiency may result in decreased vessel integrity through decreased nitric oxide synthase generation and impaired synthesis of mature collagen; potentially leading to increased plaque formation and incidence of stroke. Furthermore, an increase in infarct area may result from oxidative damage causing increased neuronal death.

Monday, September 19, 2016

A growing understanding of the connection between our gut and our brain.

Although the interaction between our brain and gut has been studied for years, its complexities run deeper than initially thought. It seems that our minds are, in some part, controlled by the bacteria in our bowels.
The gut has defenses against pathogens, but, at the same time, it encourages the survival and growth of "healthy" gut bacteria.

Of course, these bacteria do benefit from the warmth and nutrition in our bowels, but it is not a one-way relationship - they also give back.


Some species benefit us by breaking dietary fiber down into short-chain fatty acids that we can then absorb and use. They metabolize a number of compounds on our behalf and play a role in the synthesis of  vitamins B and K.
On the other hand, recent research infers that imbalance of gut bacteria might be an important factor in inflammatory and autoimmune conditions.
The microbiome's role in health and disease is only slowly giving up its secrets. The latest and perhaps most remarkable finding is the ability that gut bacteria have to moderate our brain and behavior.

The links between our gut and brain are hormonal, immunological, and neural, via the central nervous system and the enteric nervous system, which governs the function of the gut. Collectively, they are termed the gut-brain axis.

These gut-brain conversations have been studied for some time. However, a new level to this partnership has recently been glimpsed; researchers are now considering the influence of our microbiome on the gut-brain axis. In other words, researchers are asking: do the bacteria in our gut affect our psychology and behavior?

The question is whether adding beneficial gut bacteria to an animal can make a difference. Research seems to say yes.

A study published in the Journal of Neurogastroenterology and Motility, collated the results of studies looking at the effects of probiotics on central nervous system function in both humans and animals.
They examined 25 animal and 15 human studies, most of which used Bifidobacterium and Lactobacillus over a 2-4-week period. Although, as the authors mention, translating animal studies like this into human terms is a dodgy game. They concluded: "These probiotics showed efficacy in improving psychiatric disorder-related behaviors including anxiety, depression, autism spectrum disorder, obsessive compulsive disorder and memory abilities, including spatial and non-spatial memory."


Tuesday, October 14, 2014

High HDL Cholesterol Levels Associated With Reduced Alzheimer’s Risk


High levels of high-density lipoprotein (HDL), also known as “good” cholesterol, appear to be associated with a reduced risk for Alzheimer’s disease in older adults.

”Dyslipidemia [high total cholesterol and triglycerides] and late-onset Alzheimer’s disease are highly frequent in western societies,” the authors write as background information in the article. “More than 50 percent of the U.S. adult population has high cholesterol. About 1 percent of people age 65 to 69 years develop Alzheimer’s disease, and the prevalence increases to more than 60 percent for people older than 95 years.”
Christiane Reitz and colleagues studied 1,130 older adults to examine the association of blood lipid (fat) levels with Alzheimer’s disease. The study included a random sampling of Medicare recipients 65 or older residing in northern Manhattan, with no history of dementia or cognitive impairment. The researchers defined higher levels of HDL cholesterol as 55 milligrams per deciliter or more.
To determine this association, data were collected from medical, neurological and neuropsychological evaluations. Additionally, the authors assigned a diagnosis of “probable” Alzheimer’s disease when onset of dementia could not be explained by any other disorder. A diagnosis of “possible” Alzheimer’s disease was made when the most likely cause of dementia was Alzheimer’s disease but there were other disorders that could contribute to the dementia, such as stroke or Parkinson disease.
During the course of follow-up, there were 101 new cases of Alzheimer’s disease, of which 89 were probable and 12 were possible. The mean (average) age of individuals at the onset of probable and possible Alzheimer’s disease was 83 years, and compared with people who were not diagnosed with incident Alzheimer’s disease, those who did develop dementia were more often Hispanic and had a higher prevalence of diabetes at the start of the study. Higher plasma levels of HDL cholesterol were associated with a decreased risk of both probable and possible Alzheimer’s disease, even after adjusting for vascular risk factors and lipid-lowering treatments. Although higher plasma total cholesterol, non-HDL cholesterol and LDL cholesterol levels also were associated with decreased risks of probable and possible Alzheimer’s disease, these associations became non-significant after adjusting for vascular risk factors and lipid-lowering treatments.
“In this study, higher levels of HDL cholesterol were associated with a decreased risk of both probable and possible Alzheimer’s disease,” the authors conclude. “An important consideration in the interpretation of the results is that it was conducted in an urban multiethnic elderly community with a high prevalence of risk factors for mortality and dementia. Thus, our results may not be generalizeable to cohorts with younger individuals or to cohorts with participants with a lower morbidity [disease] burden.”
Arch Neurol. 2010;67(12):1491-1497. doi:10.1001/archneurol.2010.297.



Friday, May 30, 2014

Strawberry Orange Ginger Smoothie

Fresh ginger gives this smoothie a refreshing and delicious taste.


The healing properties of ginger are similar to non-steroid anti-inflammatory drugs (NSAIDs), therefore, it can regulate biochemical pathways which are activated with chronic inflammation. Adding ginger to your daily diet can soothe the aches and pain associated with aging. If you wake up with stiff joints or sore hands, this smoothie in the morning may put a smile on your face.

Ingredients

~1 cup orange juice.
~1 cup Vanilla Almond Milk
~1 tsp grated ginger root
~1 cup fresh or frozen strawberries

In a blender, combine orange juice, milk, ginger root and berries. Puree until smooth. Serve cold.
Excellent source of vitamin C, potassium and anthocyanins (antioxidants in berries).

Tip: turn this into your daily serving of Omega-3 by adding a teaspoon of Carlson’s The Very Finest Fish Oil, Orange or Lemon Flavor. Adding the Omega-3 EPA/DHA rich oil boosts the ginger's inflammation balancing power and you'll be supporting heart, brain, and vision health too! And I assure you this taste award winning oil is never fishy. Try it you'll be hooked!

Friday, May 2, 2014

Brain saving Tocotrienol: Vitamin E supplement helps 'redirect' blood during stroke.


Strokes are a leading cause of death and long term disability in the US. With the failure of more than 1,000 experimental neuroprotective drugs, one scientist has stopped trying to discover the next new stroke treatment, and instead is trying to prevent strokes from happening in the first place. Dr Cameron Rink thinks he may have found the answer in a little known member of the vitamin E family, which appears to remodel the brain’s circulatory system and provide protection the instant a stroke strikes.

During a stroke part of the brain is not getting blood or oxygen and the cells are dying. There’s not much we can do for a patient at this point and that’s frustrating,” says Rink, a professor of surgery at The Ohio State University Wexner Medical Center.

The blood vessel "redirect" is the result of 10 weeks' worth of supplementation with a little-known type of vitamin E called tocotrienol. Tocotrienol appears to stimulate arteriogenesis -- or the remodeling of existing blood vessels that can instantaneously expand in response to a demand for oxygen-rich blood. This collateral blood supply can make a major difference in stroke outcomes.


Tocotrienol, found naturally in palm oil, is a vitamin E variant and currently available in stores as an oral nutritional supplement. Because it doesn't appear to interfere with other stroke therapies like blood thinners, or have any other side effects, Rink thinks that the vitamin could someday become a common stroke prevention strategy, much like low-dose aspirin is currently recommended for cardiac patients.

Friday, April 4, 2014

Inflammation Resolution the Key to Preventing or Reversing Alzheimer's disease Suggests Compelling New Study


Supplementation with omega-3 fatty acids could help to prevent and even reverse the progression of Alzheimer’s disease. 
The connection is resolving inflammation. The beneficial fats may come to the affected person’s rescue by stimulating newly identified ‘resolution pathways’ in the brain, according to research outlining an ‘entirely new’ approach to the condition.
The new study, published in the journal Alzheimer’s & Dementia, demonstrates a new approach to dementia and Alzheimer’s disease – suggesting that omega-3 fatty acid derivatives stimulate the uptake of amyloid-beta proteins. The proteins are the alleged culprits in the deteriorating health of brains affected by this dreadful disease. They apparently kill brain cells and form Alzheimer's disease hallmark plaques.
Led by Professor Marianne Schultzberg from the Karolinska Institute, Sweden, the team behind the research revealed that normal inflammatory processes should ultimately lead to tissue repair in a process known as restoration. However, with Alzheimer's disease this normal process is interrupted – meaning that rather than repair and restore tissue, debris from dead cells and other microorganisms fails to be cleared away, and instead accumulates in the brain, wreaking havoc.
"Our hypothesis is that stimulation of resolution of inflammation in Alzheimer's disease may result in reduced neuronal death in the brain, and in turn have a beneficial effect in disease progression and cognition,” explained Schultzberg.
“This is an entirely new approach and provides the opportunity to develop new treatment principles for Alzheimer's disease," she said.
The Swedish team found protective compounds formed in the brain from omega-3 fatty acids help to induce the resolution process and stimulate the uptake or clearing away of amyloid-beta proteins that have been linked to the progression of Alzheimer's disease through the development of plaques.
The team will now try to prove the hypothesis by using animal models to see if omega-3 fatty acids can prevent memory loss and further loss of brain cells.
In the study, Dr Schultberg and her group examined cerebrospinal fluid from 15 patients with Alzheimer's disease, 20 patients with mild cognitive impairment and 21 control subjects. They also analyzed brain tissue from 10 Alzheimer's patients and 10 control subjects.
Schultzberg and her team looked for the presence, and comparative levels of several inflammatory molecules and receptors involved in the resolution pathway – including specialised pro-resolving mediators (SPMs), receptors, biosynthetic enzyme, and downstream effectors - in postmortem hippocampal tissue from AD patients and non-AD subjects.
SPMs were also measured in cerebrospinal fluid (CSF).
The team found that SPMs and SPM receptors were detected in the human brain – indicating the resolution pathway does exist in the brain. They also found that levels of the SPM lipoxin A4 (LXA4) were reduced in AD patients, both in the CSF and hippocampus.
In addition, an enzyme involved in LXA4 synthesis and two SPM receptors were elevated in AD brains, said the team, while LXA4 and RvD1 levels in CSF correlated with Mini-Mental State Examination (MMSE) scores.
As a result, the team concluded that the resolution pathway exists in the brain, adding that the alterations identified in the study “strongly suggest” a dysfunction of this pathway in Alzheimer’s disease.
They added that treatment with SPMs, or alternatively, by stimulating the resolution pathway – such as might occur with omega-3 fatty acid supplementation – “is suggested as a new and promising therapy in neurodegenerative disorders such as Alzheimer’s disease.”