Matches in SemOpenAlex for { <https://semopenalex.org/work/W2108507651> ?p ?o ?g. }
- W2108507651 endingPage "87" @default.
- W2108507651 startingPage "81" @default.
- W2108507651 abstract "Bone formation proceeds through a remodeling process that runs continuously, involving the resorption of old bone by osteoclasts, and the subsequent formation of new bone by osteoblasts. This is controlled by growth factors and cytokines produced in bone marrow microenvironment and by the action of systemic hormones, like parathyroid hormone, estradiol or growth hormone (GH). One candidate for hormonal modulation of osteoblast and osteoclast formation is melatonin. Because circulating melatonin declines with age, its possible involvement in post-menopausal and senescence osteoporosis is considered. This review article discusses early studies on melatonin-bone relationships and recent data that suggest a direct effect of melatonin on bone. Melatonin could act as an autacoid in bone cells as it is present in high quantities in bone marrow, where precursors of bone cells are located. Melatonin dose-dependently augmented proteins that are incorporated into the bone matrix, like procollagen type I c-peptide. Osteoprotegerin, an osteoblastic protein that inhibits the differentiation of osteoclasts is also augmented by melatonin in vitro. Another possible target cell for melatonin is the osteoclast, which degrades bone partly by generating free radicals. Melatonin through its free radical scavenger and antioxidant properties may impair osteoclast activity and bone resorption. At least in one study melatonin was both inhibitory to osteoclastic and osteoblastic cells. Therefore, the documented bone-protecting effect of melatonin in ovariectomized rats can depend in part on the free radical scavenging properties of melatonin. Additionally, melatonin may impair development of osteopenia associated with senescence by improving non-rapid eye movement sleep and restoring GH secretion. Whether melatonin can be used as a novel mode of therapy for augmenting bone mass in diseases deserves to be studied." @default.
- W2108507651 created "2016-06-24" @default.
- W2108507651 creator A5000726577 @default.
- W2108507651 creator A5004518697 @default.
- W2108507651 creator A5012228406 @default.
- W2108507651 creator A5049502166 @default.
- W2108507651 creator A5066104053 @default.
- W2108507651 date "2003-01-31" @default.
- W2108507651 modified "2023-10-04" @default.
- W2108507651 title "Melatonin effects on bone: experimental facts and clinical perspectives" @default.
- W2108507651 cites W1972403678 @default.
- W2108507651 cites W1974077592 @default.
- W2108507651 cites W1977934055 @default.
- W2108507651 cites W1980975664 @default.
- W2108507651 cites W1988037121 @default.
- W2108507651 cites W1989366021 @default.
- W2108507651 cites W1989386559 @default.
- W2108507651 cites W1995683291 @default.
- W2108507651 cites W1995819685 @default.
- W2108507651 cites W2000257483 @default.
- W2108507651 cites W2009699486 @default.
- W2108507651 cites W2017004213 @default.
- W2108507651 cites W2017369046 @default.
- W2108507651 cites W2020311496 @default.
- W2108507651 cites W2033417409 @default.
- W2108507651 cites W2037426688 @default.
- W2108507651 cites W2044510143 @default.
- W2108507651 cites W2047318213 @default.
- W2108507651 cites W2056122458 @default.
- W2108507651 cites W2057960878 @default.
- W2108507651 cites W2060441344 @default.
- W2108507651 cites W2060583868 @default.
- W2108507651 cites W2062014816 @default.
- W2108507651 cites W2062196582 @default.
- W2108507651 cites W2069933901 @default.
- W2108507651 cites W2072926504 @default.
- W2108507651 cites W2074028842 @default.
- W2108507651 cites W2074556387 @default.
- W2108507651 cites W2077750254 @default.
- W2108507651 cites W2085163592 @default.
- W2108507651 cites W2093501456 @default.
- W2108507651 cites W2094306240 @default.
- W2108507651 cites W2097662042 @default.
- W2108507651 cites W2098888105 @default.
- W2108507651 cites W2112916976 @default.
- W2108507651 cites W2125244567 @default.
- W2108507651 cites W2125568928 @default.
- W2108507651 cites W2139891987 @default.
- W2108507651 cites W2142616794 @default.
- W2108507651 cites W2147891066 @default.
- W2108507651 cites W2166577294 @default.
- W2108507651 cites W2178541010 @default.
- W2108507651 cites W2332799232 @default.
- W2108507651 doi "https://doi.org/10.1034/j.1600-079x.2003.00028.x" @default.
- W2108507651 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12562498" @default.
- W2108507651 hasPublicationYear "2003" @default.
- W2108507651 type Work @default.
- W2108507651 sameAs 2108507651 @default.
- W2108507651 citedByCount "208" @default.
- W2108507651 countsByYear W21085076512012 @default.
- W2108507651 countsByYear W21085076512013 @default.
- W2108507651 countsByYear W21085076512014 @default.
- W2108507651 countsByYear W21085076512015 @default.
- W2108507651 countsByYear W21085076512016 @default.
- W2108507651 countsByYear W21085076512017 @default.
- W2108507651 countsByYear W21085076512018 @default.
- W2108507651 countsByYear W21085076512019 @default.
- W2108507651 countsByYear W21085076512020 @default.
- W2108507651 countsByYear W21085076512021 @default.
- W2108507651 countsByYear W21085076512022 @default.
- W2108507651 countsByYear W21085076512023 @default.
- W2108507651 crossrefType "journal-article" @default.
- W2108507651 hasAuthorship W2108507651A5000726577 @default.
- W2108507651 hasAuthorship W2108507651A5004518697 @default.
- W2108507651 hasAuthorship W2108507651A5012228406 @default.
- W2108507651 hasAuthorship W2108507651A5049502166 @default.
- W2108507651 hasAuthorship W2108507651A5066104053 @default.
- W2108507651 hasConcept C126322002 @default.
- W2108507651 hasConcept C133605539 @default.
- W2108507651 hasConcept C134018914 @default.
- W2108507651 hasConcept C170033053 @default.
- W2108507651 hasConcept C170493617 @default.
- W2108507651 hasConcept C185592680 @default.
- W2108507651 hasConcept C202751555 @default.
- W2108507651 hasConcept C2776033226 @default.
- W2108507651 hasConcept C2776151105 @default.
- W2108507651 hasConcept C2778182776 @default.
- W2108507651 hasConcept C2778260815 @default.
- W2108507651 hasConcept C2780059843 @default.
- W2108507651 hasConcept C2781208988 @default.
- W2108507651 hasConcept C2992339995 @default.
- W2108507651 hasConcept C519063684 @default.
- W2108507651 hasConcept C55493867 @default.
- W2108507651 hasConcept C673006 @default.
- W2108507651 hasConcept C71315377 @default.
- W2108507651 hasConcept C71924100 @default.
- W2108507651 hasConcept C8264082 @default.
- W2108507651 hasConcept C86803240 @default.