THESIS
2016
xii, 75 pages : illustrations ; 30 cm
Abstract
‘Yang-invigorating’ Chinese tonifying herbs, which can increase mitochondrial ATP
generation capacity (ATP-GC) both in vitro in cardiomyocytes and in vivo in rat hearts,
may be used for promoting mitochondrial function. Psoralea Fructus (PF), a ‘Yang-invigorating’
Chinese tonifying herb, has long been used for healing bone fracture and
osteoporosis. Osteoporosis, which results from an imbalance of bone resorption and
bone formation, has been shown to be associated with mitochondrial dysfunction in
bone cells. Bone resorption and bone formation, which is involved in bone remodeling,
are carried out by osteoclasts and osteoblasts, respectively. To investigate whether the
beneficial effect of Psoralea Fructus on osteoporosis is related to the enhancement of
mitochondrial function,...[
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‘Yang-invigorating’ Chinese tonifying herbs, which can increase mitochondrial ATP
generation capacity (ATP-GC) both in vitro in cardiomyocytes and in vivo in rat hearts,
may be used for promoting mitochondrial function. Psoralea Fructus (PF), a ‘Yang-invigorating’
Chinese tonifying herb, has long been used for healing bone fracture and
osteoporosis. Osteoporosis, which results from an imbalance of bone resorption and
bone formation, has been shown to be associated with mitochondrial dysfunction in
bone cells. Bone resorption and bone formation, which is involved in bone remodeling,
are carried out by osteoclasts and osteoblasts, respectively. To investigate whether the
beneficial effect of Psoralea Fructus on osteoporosis is related to the enhancement of
mitochondrial function, an activity-guided fractionation of Psoralea Fructus was
performed using ATP-GC assay as activity monitor. Four active components were
isolated and three of them were structurally identified as psoralen, psoralidin and
corylin. The unidentified component is named PFC4. Pharmacological studies
indicated that all three identified active components (psoralen, psoralidin and corylin)
stimulated osteoblast differentiation in osteoblasts, as assessed by alkaline phosphatase
activity assay and calcium deposit assay. However, PFC4 produced no detectable effect
on osteoblast differentiation. All the four active components did not produce any
detectable changes in cell proliferation in osteoblasts. Taken together, the ability of
psoralen, psoralidin and corylin to enhance mitochondrial ATP generation capacity is
associated with the stimulation of cell differentiation in osteoblasts. The assignment of
the cause-and-effect relationship between the enhancement of mitochondrial function
and differentiation in osteoblasts awaits further investigation.
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