Annals of medicine · 2025
Melatonin combined with static magnetic field acquire better protective effects on bone mass and bone strength in osteoporosis induced by ovariectomy in rats.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Lu Hanli, Gan Nannan, Du Jun, Xue Tianle, Hou Desheng, Lu Cheng
Аннотация
OBJECTIVE: This research aimed to examine the possible impacts of Melatonin (Mel) combined with static magnetic field (SMF) on bone mass and strength in rats with osteoporosis induced by bilateral ovary removal.
METHODS: Following bilateral ovariectomy, the female ovariectomized (OVX) rats were systematically allocated into four distinct experimental groups: (1) OVX (control group), (2) OVX+melatonin (OVX+Mel), (3) OVX+magnetostatic field (OVX+SMF), and (4) OVX+melatonin/magnetostatic field (OVX+Mel/SMF). The intervention protocol consisted of daily administration of melatonin (30 mg/kg/day), exposure to a static magnetic field (50 ± 4 µT), or a combination of both treatments for a duration of 12 weeks. Upon completion of the treatment period, comprehensive biological samples were collected, including blood specimens and bilateral femurs, for subsequent multi-modal analyses. These analyses encompassed Micro-CT imaging for bone microarchitecture evaluation, histological examination for tissue morphology, biomechanical testing for bone strength assessment, serum cytokine profiling, oxidative stress marker quantification, bone metabolic marker analysis, and RT-PCR for gene expression evaluation.
RESULTS: Micro-CT evaluation indicated that OVX rats treated with Mel and SMF had significantly higher BMD, BMC BV/TV, Tb. N, and Tb. Th values, along with lower Tb. Sp than the OVX+SMF and OVX+Mel groups (all p < 0.05). Histological analysis showed that the combination of Mel and SMF notably improved trabecular quality while increasing MAR, OC, and SOD2 expression, and reducing TRAP and TNF-α levels compared to the OVX+SMF and OVX+Mel groups (all p < 0.05). Biomechanical tests demonstrated that combined treatment enhanced maximum load, stiffness, energy absorption, ultimate stress, toughness, and elastic modulus in comparison to the OVX+SMF and OVX+Mel groups (all p < 0.05). RT-PCR results revealed a significant increase in SIRT1 and OPG expression while inhibiting RANKL and SOST compared to the OVX+SMF and OVX+Mel groups (all p < 0.05). Serum tests found that this combination treatment significantly reduced levels of P1NP, CTX-1, MDA, TNF-α, and IL-6 while increasing SOD expression relative to the OVX+SMF and OVX+Mel groups (all p < 0.05).
CONCLUSION: Our results indicate that Mel combined with SMF has the potential to be an effective method for preventing bone loss and maintaining bone strength in postmenopausal osteoporosis.
METHODS: Following bilateral ovariectomy, the female ovariectomized (OVX) rats were systematically allocated into four distinct experimental groups: (1) OVX (control group), (2) OVX+melatonin (OVX+Mel), (3) OVX+magnetostatic field (OVX+SMF), and (4) OVX+melatonin/magnetostatic field (OVX+Mel/SMF). The intervention protocol consisted of daily administration of melatonin (30 mg/kg/day), exposure to a static magnetic field (50 ± 4 µT), or a combination of both treatments for a duration of 12 weeks. Upon completion of the treatment period, comprehensive biological samples were collected, including blood specimens and bilateral femurs, for subsequent multi-modal analyses. These analyses encompassed Micro-CT imaging for bone microarchitecture evaluation, histological examination for tissue morphology, biomechanical testing for bone strength assessment, serum cytokine profiling, oxidative stress marker quantification, bone metabolic marker analysis, and RT-PCR for gene expression evaluation.
RESULTS: Micro-CT evaluation indicated that OVX rats treated with Mel and SMF had significantly higher BMD, BMC BV/TV, Tb. N, and Tb. Th values, along with lower Tb. Sp than the OVX+SMF and OVX+Mel groups (all p < 0.05). Histological analysis showed that the combination of Mel and SMF notably improved trabecular quality while increasing MAR, OC, and SOD2 expression, and reducing TRAP and TNF-α levels compared to the OVX+SMF and OVX+Mel groups (all p < 0.05). Biomechanical tests demonstrated that combined treatment enhanced maximum load, stiffness, energy absorption, ultimate stress, toughness, and elastic modulus in comparison to the OVX+SMF and OVX+Mel groups (all p < 0.05). RT-PCR results revealed a significant increase in SIRT1 and OPG expression while inhibiting RANKL and SOST compared to the OVX+SMF and OVX+Mel groups (all p < 0.05). Serum tests found that this combination treatment significantly reduced levels of P1NP, CTX-1, MDA, TNF-α, and IL-6 while increasing SOD expression relative to the OVX+SMF and OVX+Mel groups (all p < 0.05).
CONCLUSION: Our results indicate that Mel combined with SMF has the potential to be an effective method for preventing bone loss and maintaining bone strength in postmenopausal osteoporosis.