fbpx
Wikipedia

Bone resorption

January 01, 1970

Bone resorption is resorption of bone tissue, that is, the process by which osteoclasts break down the tissue in bones[1] and release the minerals, resulting in a transfer of calcium from bone tissue to the blood.[2]

Bone Resorption
Light micrograph of an osteoclast displaying typical distinguishing characteristics: a large cell with multiple nuclei and a "foamy" cytosol.
SpecialtyRheumatology 

The osteoclasts are multi-nucleated cells that contain numerous mitochondria and lysosomes. These are the cells responsible for the resorption of bone. Osteoblasts are generally present on the outer layer of bone, just beneath the periosteum. Attachment of the osteoclast to the osteon begins the process. The osteoclast then induces an infolding of its cell membrane and secretes collagenase and other enzymes important in the resorption process. High levels of calcium, magnesium, phosphate and products of collagen will be released into the extracellular fluid as the osteoclasts tunnel into the mineralized bone. Osteoclasts are prominent in the tissue destruction found in psoriatic arthritis and rheumatological disorders.[3]

The human body is in a constant state of bone remodeling.[4] Bone remodeling is a process which maintains bone strength and ion homeostasis by replacing discrete parts of old bone with newly synthesized packets of proteinaceous matrix.[5] Bone is resorbed by osteoclasts, and is deposited by osteoblasts in a process called ossification.[6] Osteocyte activity plays a key role in this process. Conditions that result in a decrease in bone mass can either be caused by an increase in resorption or by a decrease in ossification. During childhood, bone formation exceeds resorption. As the aging process occurs, resorption exceeds formation.[5]

Bone resorption rates are much higher in post-menopausal older women due to estrogen deficiency related with menopause.[7] Common treatments include drugs that increase bone mineral density. Bisphosphonates, RANKL inhibitors, SERMs—selective oestrogen receptor modulators, hormone replacement therapy and calcitonin are some of the common treatments.[8] Light weight bearing exercise tends to eliminate the negative effects of bone resorption.[9]

Regulation edit

Bone resorption is highly stimulated or inhibited by signals from other parts of the body, depending on the demand for calcium.

Calcium-sensing membrane receptors in the parathyroid gland monitor calcium levels in the extracellular fluid. Low levels of calcium stimulates the release of parathyroid hormone (PTH) from chief cells of the parathyroid gland.[4] In addition to its effects on kidney and intestine, PTH increases the number and activity of osteoclasts. The increase in activity of already existing osteoclasts is the initial effect of PTH, and begins in minutes and increases over a few hours.[4] Continued elevation of PTH levels increases the abundance of osteoclasts. This leads to a greater resorption of calcium and phosphate ions.[4]

High levels of calcium in the blood, on the other hand, leads to decreased PTH release from the parathyroid gland, decreasing the number and activity of osteoclasts, resulting in less bone resorption. Vitamin D increases absorption of calcium and phosphate in the intestinal tract, leading to elevated levels of plasma calcium,[4] and thus lower bone resorption.

Calcitriol (1,25-dihydroxycholecalciferol) is the active form of vitamin D3.[10] It has numerous functions involved in blood calcium levels. Recent research indicates that calcitriol leads to a reduction in osteoclast formation, and bone resorption.[11][12] It follows that an increase in vitamin D3 intake should lead to a decrease in bone resorption — it has been shown that oral administration of vitamin D does not linearly correlate to increased serum levels of calcifediol,[13] the precursor to calcitriol.

Calcitonin is a hormone secreted by the thyroid in humans. Calcitonin decreases osteoclast activity, and decreases the formation of new osteoclasts, resulting in decreased resorption.[4] Calcitonin has a greater effect in young children than in adults, and plays a smaller role in bone remodeling than PTH.[4]

In some cases where bone resorption outpaces ossification, the bone is broken down much faster than it can be renewed. The bone becomes more porous and fragile, exposing people to the risk of fractures. Depending on where in the body bone resorption occurs, additional problems like tooth loss can arise. This can be caused by conditions such as hyperparathyroidism and hypovitaminosis D or even decreased hormonal production in the elderly. Some diseases with symptoms of decreased bone density are osteoporosis, and rickets.

Some people who experience increased bone resorption and decreased bone formation are astronauts. Due to the condition of being in a zero-gravity environment, astronauts do not need to work their musculoskeletal system as hard as when on earth. Ossification decreases due to a lack of stress, while resorption increases, leading to a net decrease in bone density.[14]

Alcoholism edit

The effects of alcohol on bone mineral density (BMD) are well-known and well-studied in animal and human populations. Through direct and indirect pathways, prolonged ethanol exposure increases fracture risk by decreasing bone mineral density and promoting osteoporosis. Indirect effects of excessive alcohol use occur via growth hormone, sex steroids, and oxidative stress.

Growth hormone is an important regulator of bone growth and remodeling in adults, and it acts via insulin-like growth factor I (IGF1) to stimulate osteoblastic differentiation.[15] Chronic alcoholism decreases the levels of IGF1, which suppresses the ability of GH to increase bone mineral density.[15]

Increasing alcohol consumption is linked with decreasing testosterone and serum estradiol levels, which in turn lead to the activation of RANK (a TNF receptor) protein that promote osteoclast formation.[16] Oxidative stress results when ethanol induces NOX expression, resulting in ROS production in osteoblasts which can ultimately result in cell senescence.[17] Direct effects of chronic alcoholism are apparent in osteoblasts, osteoclasts and osteocytes. Ethanol suppresses the activity and differentiation of osteoblasts.

At the same time, it has a direct effect on osteoclast activity. This results in an increased bone resorption rate and a decreased bone mineral density due to increased pit numbers and pit areas in the bone.[18][19][20] Research has shown that viable osteocytes (another type of bone cell) may prevent osteoclastogenesis, whereas apoptotic osteocytes tend to induce osteoclast stimulation. Stimulation of osteocyte apoptosis by alcohol exposure may explain decreased bone mineral density in chronic drinkers.[20][6]

Clinical importance edit

Bone resorption is an integral part of both physiological and pathological processes.[21]

Pathological bone resorption could be limited (local) which is induced by local inflammation,[22] for example, trauma or infection, resorption activated local factors, including growth factors, cytokines, prostaglandins, etc., are simultaneously triggered. This bone resorption could also be observed in patients with many metabolic skeleton diseases, especially osteopenia and osteoporosis, endocrine diseases, rheumatic disorders, and other cases, as well as in patients with genetic disorders.

Physiological bone resorption is an integral part of bone functioning, while the bone is constantly growing thanks to two processes — breakdown and formation of bone tissue.[23] Locally, it could be manifested in tooth eruption when the movement of a tooth follicle is followed by an active resorption of jaw bone tissue. Resorption of old bone and formation of a new one are balanced in a well-developed skeleton. However, resorption starts taking a large part in remodeling processes with age. Dentistry sees resorption as dissolution or breakdown of a tooth structure. This could be inflammation and dentine or cement loss.

Bone tissue is a dynamic system with active metabolism.[24] Bone tissue remodelling or bone remodeling is a successive chain of old bone matrix removal and its replacement with a new one.[25] These processes make a child’s skeleton grow and extend, while childhood is characterized by bone tissue growth rather than its resorption.

See also edit

References edit

  1. ^ Bone+Resorption at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  2. ^ Teitelbaum SL (September 2000). "Bone resorption by osteoclasts". Science. 289 (5484): 1504–1508. Bibcode:2000Sci...289.1504T. doi:10.1126/science.289.5484.1504. PMID 10968780.
  3. ^ Mensah KA, Schwarz EM, Ritchlin CT (August 2008). "Altered bone remodeling in psoriatic arthritis". Current Rheumatology Reports. 10 (4): 311–317. doi:10.1007/s11926-008-0050-5. PMC 2656567. PMID 18662512.
  4. ^ a b c d e f g Hall JE, Guyton AC (2011). Guyton and Hall textbook of medical physiology (12th ed.). Philadelphia, Pa: Saunders, Elsevier. ISBN 978-1-4160-4574-8.
  5. ^ a b Clarke B (November 2008). "Normal bone anatomy and physiology". Clinical Journal of the American Society of Nephrology. 3 (Suppl 3): S131–S139. doi:10.2215/CJN.04151206. PMC 3152283. PMID 18988698.
  6. ^ a b Maurel DB, Jaffre C, Rochefort GY, Aveline PC, Boisseau N, Uzbekov R, et al. (September 2011). "Low bone accrual is associated with osteocyte apoptosis in alcohol-induced osteopenia". Bone. 49 (3): 543–552. doi:10.1016/j.bone.2011.06.001. PMID 21689804.
  7. ^ Feng X, McDonald JM (2011-01-01). "Disorders of bone remodeling". Annual Review of Pathology. 6: 121–145. doi:10.1146/annurev-pathol-011110-130203. PMC 3571087. PMID 20936937.
  8. ^ Russell G, Mueller G, Shipman C, Croucher P (2001-01-01). "Clinical Disorders of Bone Resorption". The Molecular Basis of Skeletogenesis. Novartis Foundation Symposia. Vol. 232. pp. 251–267, discussion 267–271. doi:10.1002/0470846658.ch17. ISBN 9780471494331. PMID 11277085. {{cite book}}: |journal= ignored (help)
  9. ^ Shanb AA, Youssef EF (September 2014). "The impact of adding weight-bearing exercise versus nonweight bearing programs to the medical treatment of elderly patients with osteoporosis". Journal of Family & Community Medicine. 21 (3): 176–181. doi:10.4103/2230-8229.142972. PMC 4214007. PMID 25374469.
  10. ^ Institute of Medicine (US) Committee to Review Dietary Reference Intakes for Vitamin D and Calcium, Ross AC, Taylor CL, Yaktine AL, Del Valle HB (2011). "Overview of Vitamin D". In Ross AC, Taylor CL, Yaktine AL, Del Valle HB, Committee to Review Dietary Reference Intakes for Vitamin D and Calcium, Food and Nutrition Board, Institute of Medicine (eds.). Dietary Reference Intakes for Calcium and Vitamin D. Washington (DC): National Academies Press (US). doi:10.17226/13050. ISBN 978-0-309-16394-1. PMID 21796828. S2CID 58721779.
  11. ^ Kikuta J, Kawamura S, Okiji F, Shirazaki M, Sakai S, Saito H, Ishii M (April 2013). "Sphingosine-1-phosphate-mediated osteoclast precursor monocyte migration is a critical point of control in antibone-resorptive action of active vitamin D". Proceedings of the National Academy of Sciences of the United States of America. 110 (17): 7009–7013. Bibcode:2013PNAS..110.7009K. doi:10.1073/pnas.1218799110. PMC 3637769. PMID 23569273.
  12. ^ Yamamoto Y, Yoshizawa T, Fukuda T, Shirode-Fukuda Y, Yu T, Sekine K, et al. (March 2013). "Vitamin D receptor in osteoblasts is a negative regulator of bone mass control". Endocrinology. 154 (3): 1008–1020. doi:10.1210/en.2012-1542. PMID 23389957.
  13. ^ Stamp TC, Haddad JG, Twigg CA (June 1977). "Comparison of oral 25-hydroxycholecalciferol, vitamin D, and ultraviolet light as determinants of circulating 25-hydroxyvitamin D". Lancet. 1 (8026): 1341–1343. doi:10.1016/s0140-6736(77)92553-3. PMID 69059. S2CID 9326591.
  14. ^ Iwamoto J, Takeda T, Sato Y (June 2005). "Interventions to prevent bone loss in astronauts during space flight". The Keio Journal of Medicine. 54 (2): 55–59. doi:10.2302/kjm.54.55. PMID 16077253.
  15. ^ a b Maddalozzo GF, Turner RT, Edwards CH, Howe KS, Widrick JJ, Rosen CJ, Iwaniec UT (September 2009). "Alcohol alters whole body composition, inhibits bone formation, and increases bone marrow adiposity in rats". Osteoporosis International. 20 (9): 1529–1538. doi:10.1007/s00198-009-0836-y. PMID 19238309. S2CID 11502836.
  16. ^ Ronis MJ, Wands JR, Badger TM, de la Monte SM, Lang CH, Calissendorff J (August 2007). "Alcohol-induced disruption of endocrine signaling". Alcoholism: Clinical and Experimental Research. 31 (8): 1269–1285. doi:10.1111/j.1530-0277.2007.00436.x. PMID 17559547.
  17. ^ Chen JR, Shankar K, Nagarajan S, Badger TM, Ronis MJ (January 2008). "Protective effects of estradiol on ethanol-induced bone loss involve inhibition of reactive oxygen species generation in osteoblasts and downstream activation of the extracellular signal-regulated kinase/signal transducer and activator of transcription 3/receptor activator of nuclear factor-kappaB ligand signaling cascade". The Journal of Pharmacology and Experimental Therapeutics. 324 (1): 50–59. doi:10.1124/jpet.107.130351. PMID 17916759. S2CID 27152788.
  18. ^ Robling AG, Bonewald LF (February 2020). "The Osteocyte: New Insights". Annual Review of Physiology. 82 (1): 485–506. doi:10.1146/annurev-physiol-021119-034332. PMC 8274561. PMID 32040934.
  19. ^ Bonewald LF (February 2011). "The amazing osteocyte". Journal of Bone and Mineral Research. 26 (2): 229–238. doi:10.1002/jbmr.320. PMC 3179345. PMID 21254230.
  20. ^ a b Verborgt O, Tatton NA, Majeska RJ, Schaffler MB (May 2002). "Spatial distribution of Bax and Bcl-2 in osteocytes after bone fatigue: complementary roles in bone remodeling regulation?". Journal of Bone and Mineral Research. 17 (5): 907–914. doi:10.1359/jbmr.2002.17.5.907. hdl:10067/1033580151162165141. PMID 12009022. S2CID 22428635.
  21. ^ Fernández-Tresguerres-Hernández-Gil I, Alobera-Gracia MA, del-Canto-Pingarrón M, Blanco-Jerez L (March 2006). "Physiological bases of bone regeneration II. The remodeling process". Medicina Oral, Patologia Oral y Cirugia Bucal. 11 (2): E151–7. PMID 16505794.
  22. ^ Epsley S, Tadros S, Farid A, Kargilis D, Mehta S, Rajapakse CS (2020). "The Effect of Inflammation on Bone". Frontiers in Physiology. 11: 511799. doi:10.3389/fphys.2020.511799. PMC 7874051. PMID 33584321.
  23. ^ Rowe P, Koller A, Sharma S (March 2023). "Physiology, Bone Remodeling". StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. PMID 29763038. Retrieved 2023-06-07. {{cite book}}: |work= ignored (help)
  24. ^ Wawrzyniak A, Balawender K (July 2022). "Structural and Metabolic Changes in Bone". Animals. 12 (15): 1946. doi:10.3390/ani12151946. PMC 9367262. PMID 35953935.
  25. ^ Lindsay R, Cosman F (January 2007). "Pathogenesis of osteoporosis.". Treatment of the Postmenopausal Woman (3rd ed.). pp. 323–330. doi:10.1016/B978-012369443-0/50032-6. ISBN 9780123694430. Bone remodeling describes the process whereby old bone is continuously replaced by new tissue.

External links edit

January 01, 1970
bone, resorption, resorption, bone, tissue, that, process, which, osteoclasts, break, down, tissue, bones, release, minerals, resulting, transfer, calcium, from, bone, tissue, blood, bone, resorptionlight, micrograph, osteoclast, displaying, typical, distingui. Bone resorption is resorption of bone tissue that is the process by which osteoclasts break down the tissue in bones 1 and release the minerals resulting in a transfer of calcium from bone tissue to the blood 2 Bone ResorptionLight micrograph of an osteoclast displaying typical distinguishing characteristics a large cell with multiple nuclei and a foamy cytosol SpecialtyRheumatology The osteoclasts are multi nucleated cells that contain numerous mitochondria and lysosomes These are the cells responsible for the resorption of bone Osteoblasts are generally present on the outer layer of bone just beneath the periosteum Attachment of the osteoclast to the osteon begins the process The osteoclast then induces an infolding of its cell membrane and secretes collagenase and other enzymes important in the resorption process High levels of calcium magnesium phosphate and products of collagen will be released into the extracellular fluid as the osteoclasts tunnel into the mineralized bone Osteoclasts are prominent in the tissue destruction found in psoriatic arthritis and rheumatological disorders 3 The human body is in a constant state of bone remodeling 4 Bone remodeling is a process which maintains bone strength and ion homeostasis by replacing discrete parts of old bone with newly synthesized packets of proteinaceous matrix 5 Bone is resorbed by osteoclasts and is deposited by osteoblasts in a process called ossification 6 Osteocyte activity plays a key role in this process Conditions that result in a decrease in bone mass can either be caused by an increase in resorption or by a decrease in ossification During childhood bone formation exceeds resorption As the aging process occurs resorption exceeds formation 5 Bone resorption rates are much higher in post menopausal older women due to estrogen deficiency related with menopause 7 Common treatments include drugs that increase bone mineral density Bisphosphonates RANKL inhibitors SERMs selective oestrogen receptor modulators hormone replacement therapy and calcitonin are some of the common treatments 8 Light weight bearing exercise tends to eliminate the negative effects of bone resorption 9 Contents 1 Regulation 2 Alcoholism 3 Clinical importance 4 See also 5 References 6 External linksRegulation editBone resorption is highly stimulated or inhibited by signals from other parts of the body depending on the demand for calcium Calcium sensing membrane receptors in the parathyroid gland monitor calcium levels in the extracellular fluid Low levels of calcium stimulates the release of parathyroid hormone PTH from chief cells of the parathyroid gland 4 In addition to its effects on kidney and intestine PTH increases the number and activity of osteoclasts The increase in activity of already existing osteoclasts is the initial effect of PTH and begins in minutes and increases over a few hours 4 Continued elevation of PTH levels increases the abundance of osteoclasts This leads to a greater resorption of calcium and phosphate ions 4 High levels of calcium in the blood on the other hand leads to decreased PTH release from the parathyroid gland decreasing the number and activity of osteoclasts resulting in less bone resorption Vitamin D increases absorption of calcium and phosphate in the intestinal tract leading to elevated levels of plasma calcium 4 and thus lower bone resorption Calcitriol 1 25 dihydroxycholecalciferol is the active form of vitamin D3 10 It has numerous functions involved in blood calcium levels Recent research indicates that calcitriol leads to a reduction in osteoclast formation and bone resorption 11 12 It follows that an increase in vitamin D3 intake should lead to a decrease in bone resorption it has been shown that oral administration of vitamin D does not linearly correlate to increased serum levels of calcifediol 13 the precursor to calcitriol Calcitonin is a hormone secreted by the thyroid in humans Calcitonin decreases osteoclast activity and decreases the formation of new osteoclasts resulting in decreased resorption 4 Calcitonin has a greater effect in young children than in adults and plays a smaller role in bone remodeling than PTH 4 In some cases where bone resorption outpaces ossification the bone is broken down much faster than it can be renewed The bone becomes more porous and fragile exposing people to the risk of fractures Depending on where in the body bone resorption occurs additional problems like tooth loss can arise This can be caused by conditions such as hyperparathyroidism and hypovitaminosis D or even decreased hormonal production in the elderly Some diseases with symptoms of decreased bone density are osteoporosis and rickets Some people who experience increased bone resorption and decreased bone formation are astronauts Due to the condition of being in a zero gravity environment astronauts do not need to work their musculoskeletal system as hard as when on earth Ossification decreases due to a lack of stress while resorption increases leading to a net decrease in bone density 14 Alcoholism editThe effects of alcohol on bone mineral density BMD are well known and well studied in animal and human populations Through direct and indirect pathways prolonged ethanol exposure increases fracture risk by decreasing bone mineral density and promoting osteoporosis Indirect effects of excessive alcohol use occur via growth hormone sex steroids and oxidative stress Growth hormone is an important regulator of bone growth and remodeling in adults and it acts via insulin like growth factor I IGF1 to stimulate osteoblastic differentiation 15 Chronic alcoholism decreases the levels of IGF1 which suppresses the ability of GH to increase bone mineral density 15 Increasing alcohol consumption is linked with decreasing testosterone and serum estradiol levels which in turn lead to the activation of RANK a TNF receptor protein that promote osteoclast formation 16 Oxidative stress results when ethanol induces NOX expression resulting in ROS production in osteoblasts which can ultimately result in cell senescence 17 Direct effects of chronic alcoholism are apparent in osteoblasts osteoclasts and osteocytes Ethanol suppresses the activity and differentiation of osteoblasts At the same time it has a direct effect on osteoclast activity This results in an increased bone resorption rate and a decreased bone mineral density due to increased pit numbers and pit areas in the bone 18 19 20 Research has shown that viable osteocytes another type of bone cell may prevent osteoclastogenesis whereas apoptotic osteocytes tend to induce osteoclast stimulation Stimulation of osteocyte apoptosis by alcohol exposure may explain decreased bone mineral density in chronic drinkers 20 6 Clinical importance editBone resorption is an integral part of both physiological and pathological processes 21 Pathological bone resorption could be limited local which is induced by local inflammation 22 for example trauma or infection resorption activated local factors including growth factors cytokines prostaglandins etc are simultaneously triggered This bone resorption could also be observed in patients with many metabolic skeleton diseases especially osteopenia and osteoporosis endocrine diseases rheumatic disorders and other cases as well as in patients with genetic disorders Physiological bone resorption is an integral part of bone functioning while the bone is constantly growing thanks to two processes breakdown and formation of bone tissue 23 Locally it could be manifested in tooth eruption when the movement of a tooth follicle is followed by an active resorption of jaw bone tissue Resorption of old bone and formation of a new one are balanced in a well developed skeleton However resorption starts taking a large part in remodeling processes with age Dentistry sees resorption as dissolution or breakdown of a tooth structure This could be inflammation and dentine or cement loss Bone tissue is a dynamic system with active metabolism 24 Bone tissue remodelling or bone remodeling is a successive chain of old bone matrix removal and its replacement with a new one 25 These processes make a child s skeleton grow and extend while childhood is characterized by bone tissue growth rather than its resorption See also editBone remodeling Nuclear factor kappa BReferences edit Bone Resorption at the U S National Library of Medicine Medical Subject Headings MeSH Teitelbaum SL September 2000 Bone resorption by osteoclasts Science 289 5484 1504 1508 Bibcode 2000Sci 289 1504T doi 10 1126 science 289 5484 1504 PMID 10968780 Mensah KA Schwarz EM Ritchlin CT August 2008 Altered bone remodeling in psoriatic arthritis Current Rheumatology Reports 10 4 311 317 doi 10 1007 s11926 008 0050 5 PMC 2656567 PMID 18662512 a b c d e f g Hall JE Guyton AC 2011 Guyton and Hall textbook of medical physiology 12th ed Philadelphia Pa Saunders Elsevier ISBN 978 1 4160 4574 8 a b Clarke B November 2008 Normal bone anatomy and physiology Clinical Journal of the American Society of Nephrology 3 Suppl 3 S131 S139 doi 10 2215 CJN 04151206 PMC 3152283 PMID 18988698 a b Maurel DB Jaffre C Rochefort GY Aveline PC Boisseau N Uzbekov R et al September 2011 Low bone accrual is associated with osteocyte apoptosis in alcohol induced osteopenia Bone 49 3 543 552 doi 10 1016 j bone 2011 06 001 PMID 21689804 Feng X McDonald JM 2011 01 01 Disorders of bone remodeling Annual Review of Pathology 6 121 145 doi 10 1146 annurev pathol 011110 130203 PMC 3571087 PMID 20936937 Russell G Mueller G Shipman C Croucher P 2001 01 01 Clinical Disorders of Bone Resorption The Molecular Basis of Skeletogenesis Novartis Foundation Symposia Vol 232 pp 251 267 discussion 267 271 doi 10 1002 0470846658 ch17 ISBN 9780471494331 PMID 11277085 a href Template Cite book html title Template Cite book cite book a journal ignored help Shanb AA Youssef EF September 2014 The impact of adding weight bearing exercise versus nonweight bearing programs to the medical treatment of elderly patients with osteoporosis Journal of Family amp Community Medicine 21 3 176 181 doi 10 4103 2230 8229 142972 PMC 4214007 PMID 25374469 Institute of Medicine US Committee to Review Dietary Reference Intakes for Vitamin D and Calcium Ross AC Taylor CL Yaktine AL Del Valle HB 2011 Overview of Vitamin D In Ross AC Taylor CL Yaktine AL Del Valle HB Committee to Review Dietary Reference Intakes for Vitamin D and Calcium Food and Nutrition Board Institute of Medicine eds Dietary Reference Intakes for Calcium and Vitamin D Washington DC National Academies Press US doi 10 17226 13050 ISBN 978 0 309 16394 1 PMID 21796828 S2CID 58721779 Kikuta J Kawamura S Okiji F Shirazaki M Sakai S Saito H Ishii M April 2013 Sphingosine 1 phosphate mediated osteoclast precursor monocyte migration is a critical point of control in antibone resorptive action of active vitamin D Proceedings of the National Academy of Sciences of the United States of America 110 17 7009 7013 Bibcode 2013PNAS 110 7009K doi 10 1073 pnas 1218799110 PMC 3637769 PMID 23569273 Yamamoto Y Yoshizawa T Fukuda T Shirode Fukuda Y Yu T Sekine K et al March 2013 Vitamin D receptor in osteoblasts is a negative regulator of bone mass control Endocrinology 154 3 1008 1020 doi 10 1210 en 2012 1542 PMID 23389957 Stamp TC Haddad JG Twigg CA June 1977 Comparison of oral 25 hydroxycholecalciferol vitamin D and ultraviolet light as determinants of circulating 25 hydroxyvitamin D Lancet 1 8026 1341 1343 doi 10 1016 s0140 6736 77 92553 3 PMID 69059 S2CID 9326591 Iwamoto J Takeda T Sato Y June 2005 Interventions to prevent bone loss in astronauts during space flight The Keio Journal of Medicine 54 2 55 59 doi 10 2302 kjm 54 55 PMID 16077253 a b Maddalozzo GF Turner RT Edwards CH Howe KS Widrick JJ Rosen CJ Iwaniec UT September 2009 Alcohol alters whole body composition inhibits bone formation and increases bone marrow adiposity in rats Osteoporosis International 20 9 1529 1538 doi 10 1007 s00198 009 0836 y PMID 19238309 S2CID 11502836 Ronis MJ Wands JR Badger TM de la Monte SM Lang CH Calissendorff J August 2007 Alcohol induced disruption of endocrine signaling Alcoholism Clinical and Experimental Research 31 8 1269 1285 doi 10 1111 j 1530 0277 2007 00436 x PMID 17559547 Chen JR Shankar K Nagarajan S Badger TM Ronis MJ January 2008 Protective effects of estradiol on ethanol induced bone loss involve inhibition of reactive oxygen species generation in osteoblasts and downstream activation of the extracellular signal regulated kinase signal transducer and activator of transcription 3 receptor activator of nuclear factor kappaB ligand signaling cascade The Journal of Pharmacology and Experimental Therapeutics 324 1 50 59 doi 10 1124 jpet 107 130351 PMID 17916759 S2CID 27152788 Robling AG Bonewald LF February 2020 The Osteocyte New Insights Annual Review of Physiology 82 1 485 506 doi 10 1146 annurev physiol 021119 034332 PMC 8274561 PMID 32040934 Bonewald LF February 2011 The amazing osteocyte Journal of Bone and Mineral Research 26 2 229 238 doi 10 1002 jbmr 320 PMC 3179345 PMID 21254230 a b Verborgt O Tatton NA Majeska RJ Schaffler MB May 2002 Spatial distribution of Bax and Bcl 2 in osteocytes after bone fatigue complementary roles in bone remodeling regulation Journal of Bone and Mineral Research 17 5 907 914 doi 10 1359 jbmr 2002 17 5 907 hdl 10067 1033580151162165141 PMID 12009022 S2CID 22428635 Fernandez Tresguerres Hernandez Gil I Alobera Gracia MA del Canto Pingarron M Blanco Jerez L March 2006 Physiological bases of bone regeneration II The remodeling process Medicina Oral Patologia Oral y Cirugia Bucal 11 2 E151 7 PMID 16505794 Epsley S Tadros S Farid A Kargilis D Mehta S Rajapakse CS 2020 The Effect of Inflammation on Bone Frontiers in Physiology 11 511799 doi 10 3389 fphys 2020 511799 PMC 7874051 PMID 33584321 Rowe P Koller A Sharma S March 2023 Physiology Bone Remodeling StatPearls Internet Treasure Island FL StatPearls Publishing PMID 29763038 Retrieved 2023 06 07 a href Template Cite book html title Template Cite book cite book a work ignored help Wawrzyniak A Balawender K July 2022 Structural and Metabolic Changes in Bone Animals 12 15 1946 doi 10 3390 ani12151946 PMC 9367262 PMID 35953935 Lindsay R Cosman F January 2007 Pathogenesis of osteoporosis Treatment of the Postmenopausal Woman 3rd ed pp 323 330 doi 10 1016 B978 012369443 0 50032 6 ISBN 9780123694430 Bone remodeling describes the process whereby old bone is continuously replaced by new tissue External links edit Retrieved from https en wikipedia org w index php title Bone resorption amp oldid 1182883496, wikipedia, wiki, book, books, library,

article

, read, download, free, free download, mp3, video, mp4, 3gp, jpg, jpeg, gif, png, picture, music, song, movie, book, game, games.