Guest guest Posted July 29, 2006 Report Share Posted July 29, 2006 Hi JoAnn (if you're still here), I was looking up " parathyroid " on this site and found some of your very infomrative articles with the below mentioned from almost exactly 13 months ago. I've been doing a lot of reading on hyperparathyroidism and how it takes calcium from the bones. In fact I have a rather high serum calcium. What surprised me in the article was that calcitrol may not be the answer. I also suspect that other endocrine glands are implicated, like insulin and have read that this indeed may be the case. According to the article, estrogen and now Vitamin K are the good guys. If you're reading this or anyone else, can you please direct me to other links where I can get more information? Thanks and regards, Janet , JoAnn Guest <angelprincessjo wrote: > > The Calcium-hormones JoAnn Guest Jun 28, 2005 16:53 PDT > The calcium-hormones function like a fire brigade; when structurally > little calcium is consumed, they aren't activated that much, which is > good ; no fire. > > When too much calcium is consumed, the calcium-hormones are very active, > stimulating absorption of calcium into the bones, and subsequently > deportation and excretion. And the more this processed is enhanced, the > more the bones erode. > After calcium is absorbed, calcitonine (or thyrocalcitonine) inhibits > deportation of calcium from the bones, whilst the calcium automatically > keeps pouring in. Calcitonine also stimulates excretion of calcium > through urinating. > > So, calcitonine primarily lowers blood-calcium level, and absorption of > calcium into the bones is one way to reach that goal. Absorbing calcium > into the bones certainly is not the purpose of calcitonine, for it > stimulates excretion of calcium too. > > Due to the action of calcitonine, the increased blood-calcium level > decreases, inhibiting calcitonine release and stimulating secretion of > two other calcium-hormones; PTH and calcitriol. > Parathyroid hormone (PTH) stimulates uptake of calcium into the bones > (1) (and therefore osteoblast apoptosis (2)) and deportation of calcium > from the bones, and inhibits excretion of calcium, generally increasing > a low blood-calcium level. Logically, elevated PTH level accelerates > ageing of the bones; see hyperparathyroidism > > Low levels of PTH prevent bone loss. (3) > > PTH also stimulates secretion of calcitriol; > Calcitriol (1,25 dihydroxycholecalciferol = composed of vit. D); The > direct influence of calcitriol is increasing the uptake of dietary > calcium into the blood, but also the uptake of calcium into the bones > (4) (Calcitriol therefore also increases osteoblasts apoptosis (5)) and > deportation of calcium from the bones. > > > > Calcitriol however also inhibits secretion of PTH. And since the > stimulating effect of PTH on the uptake of calcium into the bones and > the subsequent deportation, supplementary calcitriol can, per saldo, in > fact strongly decrease uptake of calcium into the bones and subsequent > deportation. (6) Since calcitriol also increases intestinal calcium > absorption, this however also strongly increases blood-calcium level > (7). > > > > Too much calcium in the blood can precipitate in the arteries, joints > and ligaments and kills muscle cells (since muscle cells can only > contract by deporting calcium outside the muscle-cells, which is harder > if the blood contains more calcium). Too much calcitriol / vitamin D can > cause arteriosclerosis, bone-deformation (8), muscle cramps and > fibromyalgia. > Estrogen > > Estrogens are multi-functional hormones, and one of their functions > involves the bones. > > The calcium-hormones mentioned above, induce circulation of calcium; > from the blood into the bones and vice versa, `pumping' the calcium > around. Estrogens are the brakes on this system, to minimize erosion. > > > > Calcium is absorbed into the bones due to osteoblasts, which increase > free phosphate level in the bones, which causes the `passive' influx of > calcium, to restore the calcium-phosphate ratio. > > Deportation of calcium from the bones by osteoclasts is an active > process. > > Structurally, estrogen does not stimulate osteoblasts (9) , but even > inhibits osteoblast activity (10) and therefore inhibits calcium influx > in the bones (11) and also inhibits deportation of calcium from the > bones. Thus estrogen protects the bones against excessive bone turnover, > and osteoblasts against apoptosis. > > Estrogen prevents death of osteoblasts in particular because osteoblasts > are more sensitive to ageing phenomena than osteoclasts. (12) > In general, this protective effect of estrogen is accredited to the > decrease in deportation of calcium from the bones, and is the inhibitory > effect of estrogen on calcium influx ignored. > > But a characteristic action of estrogens on the skeleton is inhibition > of longitudinal bone growth. (13) > > Some claim that estrogen increases calcium influx in the bones, but this > is only the case in the first 6 days of administration. (9) > The reason why osteoporosis risk in women is higher than in men, > regardless of menopause and milk consumption, is due to monthly estrogen and PTH fluctuations; > > Estrogen levels in women strongly fluctuate monthly. > > As estrogen level is at its lowest (around menstruation), PTH level is > at its highest, increasing deportation of calcium from the bones. (14) > (and uptake of calcium into the bones) > > Thus lifetime bone turnover averagely is higher in women. > Vitamin K > > Vitamin K seems to be protective for inhibiting death of osteoblasts. > (15) But how exactly this happens, remains unclear; vitamin K may > inhibit fractional calcium absorption and therefore prevent osteoblast > apoptosis. Or vitamin K may reduce `unnecessary' apoptosis of > osteoblasts even without excessive calcium turnover. Vitamin K can > however also increase osteoblast apoptosis. (16) > > Vitamin K does not affect intestinal calcium absorption (17), but the > intake of dietary vitamin K2 has a preventive effect on bone resorption > caused by ovariectomie or a lack of vitamin K, and in postmenopausal > women. Quote Link to comment Share on other sites More sharing options...
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