Division of Endocrinology and Center for Research in Anabolic Skeletal Target in Health and Illness (ASTHI), CSIR-Central Drug Research Institute, Council of Scientific and Industrial Research, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow, 226031, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
Calcif Tissue Int. 2022 Aug;111(2):196-210. doi: 10.1007/s00223-022-00979-9. Epub 2022 Apr 22.
Isovitexin (apigenin-6C-glucopyranose) is found in several food items and medicinal plants. Recently, we showed that isovitexin stimulated osteoblast differentiation through mitochondrial biogenesis and respiration that required adiponectin receptors (AdipoRs). Here, we studied whether oral isovitexin has a bone anabolic effect in vivo. At first, using a femur osteotomy model in adult mice, we compared the bone regenerative effect of isovitexin and apigenin. Whereas isovitexin-stimulated bone formation at the osteotomy site at 2.5 mg/kg and 5 mg/kg dose, apigenin had no effect. Subsequently, we tested the effect of isovitexin (5 mg/kg) in ovariectomized (OVX) osteopenic mice and observed that it restored bone mass and architecture of trabecular bones (femur metaphysis and fifth lumbar vertebra/L5) and cortical bones (femur diaphysis). Isovitexin completely restored bone strength at L5 (compressive strength) and femur (bending strength) in OVX mice. The bone anabolic effect of isovitexin was demonstrated by the increased surface referent bone formation parameters, increased expression of osteogenic genes (Runx2, bone morphogenetic protein-2 and type 1 collagen) in bones, and increased serum procollagen type 1N-terminal propeptide in OVX mice and these were on a par with teriparatide. Isovitexin inhibited bone and serum sclerostin as well as the serum type I collagen cross-linked C-telopeptide in OVX mice. Isovitexin has an oral bioavailability of 14.58%. Taken together, our data show that isovitexin had a significant oral bioavailability that translated to osteoanabolic effect equivalent to teriparatide and inhibited bone resorption, which implied a durable effect over teriparatide.
异荭草苷(芹菜素-6C-葡萄糖苷)存在于几种食品和药用植物中。最近,我们发现异荭草苷通过需要脂联素受体(AdipoRs)的线粒体生物发生和呼吸来刺激成骨细胞分化。在这里,我们研究了异荭草苷在体内是否具有骨合成代谢作用。首先,我们在成年小鼠股骨切开模型中比较了异荭草苷和芹菜素的骨再生作用。尽管异荭草苷在 2.5mg/kg 和 5mg/kg 剂量下刺激了骨切开部位的骨形成,但芹菜素没有效果。随后,我们测试了异荭草苷(5mg/kg)对去卵巢(OVX)骨质疏松小鼠的作用,观察到它恢复了小梁骨(股骨骨骺和第五腰椎/L5)和皮质骨(股骨骨干)的骨量和结构。异荭草苷完全恢复了 OVX 小鼠 L5(抗压强度)和股骨(弯曲强度)的骨强度。异荭草苷的骨合成代谢作用通过增加表面参照骨形成参数、骨中成骨基因(Runx2、骨形态发生蛋白-2 和 I 型胶原)的表达以及增加 OVX 小鼠血清前胶原 I 型 N 端前肽来证明,与特立帕肽相当。异荭草苷抑制了 OVX 小鼠的骨和血清骨硬化素以及血清 I 型胶原交联 C-端肽。异荭草苷的口服生物利用度为 14.58%。总之,我们的数据表明,异荭草苷具有显著的口服生物利用度,可转化为与特立帕肽相当的成骨作用,并抑制骨吸收,这意味着其作用比特立帕肽更持久。