Journal of Molecular Endocrinology (2011) 4663-66
© 2011 Society for Endocrinology
Direct suppression of Pth gene expression by the vitamin D prohormones doxercalciferol and calcidiol requires the vitamin D receptor
Cynthia S Ritter and Alex J Brown
Renal Division, Washington University School of Medicine, PO Box 8126, 660 South Euclid, St Louis, Missouri 63110, USA
Vitamin D compounds regulate PTH at the transcriptional level, presumably via binding to the vitamin D receptor (VDR), but the exact mechanism is presently unclear. We recently reported that the several vitamin D prohormones with low VDR affinity suppressed PTH, even when their activation was inhibited, raising the possibility that their actions may be VDR independent. To test this hypothesis, we developed a novel organ culture that allowed the assessment of activities of the prohormones on PTH release from wild-type and VDR-null thyroparathyroid explants. The cultures remained viable with respect to PTH release for at least 2 weeks. Full suppression of PTH by the native vitamin D hormone, 1,25-dihydroxyvitamin D3 [1,25 (OH)2D3], required 2 days, consistent with a transcriptional mechanism, and was reversible, indicating that reduced PTH was not attributable to cell death. Inhibition of PTH release by 1,25 (OH)2D3 and two prohormones, 25-hydroxyvitamin D3 and 1-hydroxyvitamin D2, was observed in explants from wild-type mice but not in those from VDR-null mice. These findings 1) are the first direct demonstration of the role of the VDR in regulation of PTH by 1,25(OH)2D3, 2) confirm that the suppressive actions of the vitamin D prohormones are mediated by the VDR, and 3) introduce a novel organ culture model that allows the ex vivo study of the function of parathyroid glands from transgenic animals.
To lower parathyroid hormone (PTH) levels, it's important to address the underlying cause, such as vitamin D deficiency or chronic kidney disease. Increasing dietary calcium and vitamin D intake can help, as these nutrients play a crucial role in regulating PTH. Additionally, medications like calcimimetics may be prescribed for conditions like secondary hyperparathyroidism. Regular check-ups with a healthcare professional are essential for monitoring and managing PTH levels effectively.
Bones: PTH increases bone resorption, releasing calcium and phosphorus into the bloodstream. Kidneys: PTH stimulates the reabsorption of calcium and the excretion of phosphorus in the kidneys. Intestine: PTH indirectly promotes calcium absorption in the intestine through its actions on vitamin D.
Parathyroid hormone (PTH) primarily acts on osteoblasts and osteoclasts in bone tissue, as well as on the kidneys to regulate calcium and phosphate levels in the body. Additionally, PTH can stimulate the production of vitamin D in the kidneys.
PTH is released when the body senses low serum calcium levels. PTH does everything in its power to increase serum calcium- it rips it from bone, increases its absorption from food, increases VIT D production (which also aids calcium absorption) and reduces its excretion from the body in urine. It therefore reduces urinary calcium.Above it was stated that PTH increases vit D production.This is wrong. Exposure of the skin to sunlight when the angle isn't too low and certain foods and supplements increase vit D. When serum calcium is low, PTH is sent by the parathyroids to signal vitamin D to activate itself and enable calcium absorption. When there is sufficient dietary calcium and vitamin D, serum calcium rises appropriately, and PTH is then decreased. When there is not enough dietary calcium and vitamin D, PTH can't get the calcium it needs. PTH then goes to the kidneys to look for temporarily stored calcium. If there isn't enough there, it goes to the bone to get the calcium there. Urinary calcium is from excess calcium that is absorbed into the blood with help from vitamin D (and thyroid) or absorbed when the bone is broken down. I learned that when urinary calcium is very high (above 300), PTH is high, but serum calcium is normal, this may indicate primary hyperparathryoidism even if serum calcium is normal. Good luck finding a doctor who will look further into primary hyperparathyroidism for patients without high serum calcium, regardless of high PTH and high urine calcium.
Parathyroid hormone (PTH) is the hormone that activates vitamin D in response to low blood calcium levels. This activation of vitamin D helps to increase calcium absorption in the intestines and maintain normal calcium levels in the blood.
Excessive production of parathyroid hormone (PTH) can lead to demineralization of bones and increase the risk of spontaneous fractures. This condition is known as hyperparathyroidism.
The three main factors responsible for regulating calcium levels in the body are parathyroid hormone (PTH), vitamin D, and calcitonin. PTH increases calcium levels in the blood by promoting its release from bones and increasing its absorption in the intestines. Vitamin D assists in calcium absorption in the intestines, while calcitonin helps to lower blood calcium levels by inhibiting bone breakdown.
Parathyroid hormone (PTH) levels typically follow a diurnal pattern, with higher levels early in the morning and lower levels in the afternoon and evening. This pattern is influenced by factors such as calcium levels in the blood, vitamin D status, and feedback mechanisms that regulate PTH secretion.
Vitamin D is produced by ultraviolet radiation on your skin. The UV light converts a precursor molecule to vitamin D.
The parathyroid hormone stimulates the absorption of calcium from the bone.
Vitamin D (disambiguation).
I know that vitamin d is one isn't vitamin e another?