Medical Researches
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Based on 11 Researches
Vitamin D improves heart healthThe Effect of Vitamin D Deficiency Treatment on Lipid Profile and C-reactive Protein in Patients with Ischemic Heart Disease: Double-blind Randomized Clinical Trial.
Study shows vitamin D benefits
We conducted a double-blind, randomized clinical trial to explore how treating vitamin D deficiency affects heart health, specifically in patients with ischemic heart disease (IHD). In our study, we involved 44 patients aged between 40 and 65 who were dealing with low vitamin D levels. They were divided into two groups—one receiving vitamin D supplements and the other a placebo.
Over five weeks, patients in the intervention group received weekly doses of 50,000 units of vitamin D. We measured changes in their lipid profiles, which includes important markers like cholesterol and triglycerides, as well as C-reactive protein (CRP), an indicator of inflammation.
Our findings revealed that vitamin D supplementation led to significant improvements. Patients in the intervention group showed an increase in good cholesterol (HDL) and a decrease in triglycerides, which are both beneficial for heart health. While the placebo group also experienced some minor improvements, the notable changes were primarily in the group receiving vitamin D.
Overall, these results suggest that addressing vitamin D deficiency can have positive effects on lipid levels in IHD patients. This is an encouraging insight for healthcare providers looking to manage heart disease risk more effectively.
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Vitamin D3 shows potential heart protectionElectrocardiographic, biochemical, and scintigraphic evidence for the cardioprotective effect of paricalcitol and vitamin D3 on doxorubicin-induced acute cardiotoxicity in rats.
Study details vitamin D3 usage
We explored the effects of vitamin D3 and paricalcitol on heart health, particularly in the context of doxorubicin-induced cardiotoxicity. In our study, we worked with male Wistar rats divided into various groups, some receiving doxorubicin, a drug known for its heart-damaging potential. Others were treated with vitamin D3 or paricalcitol, both thought to have protective qualities against heart injury.
After administering doxorubicin, we observed significant changes in a range of biochemical markers and physiological indicators, including ECG readings and scintigraphy results. The findings suggested that both vitamin D3 and paricalcitol demonstrate potential cardioprotective effects by reducing inflammation and oxidative stress linked to heart damage.
This study shines a light on the possible benefits of vitamin D3 in protecting the heart during chemotherapy treatments. However, readers should note that while our findings are promising, they stem from an animal model, and further research is needed to confirm these effects in humans.
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Vitamin D3 offers cardiac protectionCardioprotective effect of vitamin D3 on cisplatin-induced cardiotoxicity in male mice: role of oxidative stress.
Study highlights vitamin D3 benefits.
We examined how vitamin D3 could play a role in protecting the heart from damage caused by cisplatin, a chemotherapy drug. In our research, we worked with male Balb-c mice, dividing them into several groups to evaluate different treatment approaches. Some groups received vitamin D3 before or after cisplatin injection, while others acted as controls.
Our findings revealed that cisplatin significantly raised markers indicating heart damage and increased oxidative stress levels. In contrast, when we administered vitamin D3, whether as a preventive measure or treatment after cisplatin exposure, it showed promising results. It was able to improve heart tissue structure and biochemical indicators associated with heart injury, suggesting that vitamin D3 may mitigate some of the cardiac risks linked with chemotherapy.
However, while vitamin D3 showed a protective effect in the groups that received it before cisplatin treatment, the benefits were only partial when given afterward. This highlights the potential of vitamin D3 in supporting heart health during cancer treatment, although more research is necessary to understand its full capabilities and best applications.
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Vitamin D3's cardiomyoblast protectionSirtuin 1 mediates the pro-survival effects of vitamin D in angiotensin II-induced hypertrophy of H9c2 cardiomyoblasts.
Explores vitamin D3 and hypertrophy
We explored the effects of vitamin D3, a vital nutrient, on heart health, particularly in relation to a common risk factor known as angiotensin II. Our study focused on H9c2 cardiomyoblasts, a type of heart cell, to understand how vitamin D3 interacts with this condition.
By exposing these cells to angiotensin II along with vitamin D3, we aimed to see if the vitamin could shield the cells from damage. Interestingly, we found that vitamin D3 showed significant potential for preventing cell damage when SIRT1, a protein involved in cell survival, was present. However, when we blocked SIRT1, vitamin D3 wasn’t able to protect the heart cells effectively against the harmful effects induced by angiotensin II.
While vitamin D3 did help mitigate some effects of hypertrophy, or heart cell enlargement, it was clear that SIRT1 was crucial for the vitamin's protective benefits. This finding suggests that enhancing SIRT1 activity could be an exciting path forward for developing treatments to combat heart disease linked to hypertrophy and other conditions related to angiotensin II.
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Vitamin D's protective heart rolePharmacologic or genetic interference with atrogene signaling protects against glucocorticoid-induced musculoskeletal and cardiac disease.
Low relevance to vitamin D3 effects
We delved into how vitamin D, specifically its receptor activation with ligands like calcitriol, influences heart health when glucocorticoids are involved. Our research showed that glucocorticoids, while effective as immunosuppressants, can harm the musculoskeletal and cardiac systems, leading to significant issues such as falls, fractures, and cardiovascular events in long-term users.
Notably, we discovered that glucocorticoids trigger the expression of certain proteins, known as atrogenes, in bones, muscles, and the heart, which promote protein degradation. However, activating the vitamin D receptor helped prevent this negative response in all three tissues. This protective effect was also supported by the use of carfilzomib, which inhibits the proteasome directly.
Additionally, when we looked at genetic changes alongside glucocorticoid treatment, we noted that mice lacking a specific atrogene, MuRF1, experienced less damage in their skeletal and heart muscles. This suggests that targeting the pathway related to MuRF1 may offer a strategy to cushion the adverse impacts of glucocorticoids on these tissues. Ultimately, our findings highlight vitamin D’s potential role in safeguarding heart and muscle health amidst glucocorticoid treatment.
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User Reviews
Good composition. No vitamin enhances health like vitamin D (vitamin D3 or cholecalciferol). Research indicates that vitamin D may be vital in preventing SARS or upper respiratory infections. Studies show that higher vitamin D levels in blood are associated with a reduced risk of heart disease, breast cancer, and diabetes. I purchased vitamin D3 for the pandemic. The tablets are small and easy to swallow, ideally taken with fatty foods. I took a large dose of 5000 units.
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A good product that I use for my knee pain. It acts similarly to anti-inflammatory drugs like ibuprofen. Vitamin D in large doses can help control inflammatory diseases. My father took it when hospitalised in intensive care and survived—a true miracle. Vitamin D from food or sunlight is essential for everyone and serves as a significant immune booster.
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It's time for Iherba to consider the dosages of this brand! This vitamin helped alleviate cramps throughout my body. I recommend getting tested before taking it, as an overdose is more severe than a deficiency. Vitamin D is crucial in combating autoimmune diseases and should be taken to prevent Covid and after recovery. DO NOT INCREASE THE DOSE!
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