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A Rat Model of Mild Intrauterine Hypoperfusion with Microcoil Stenosis
Published on: January 7, 2018
Effects of hyperhomocysteinemia during the gestational period on ossification in rat embryo
Zabih Allah Azizi1, Ali Zamani, Ladan R Omrani
1Endocrine and Metabolism Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Insights
Maternal hyperhomocysteinemia, a condition of high homocysteine levels, leads to reduced bone volume and altered growth plate development in newborn rats, indicating potential fetal bone defects.
Area of Science:
- Endocrinology and Metabolism
- Developmental Biology
- Orthopedics
Background:
- Severe hyperhomocysteinemia, as seen in homocystinuria, is linked to skeletal malformations and osteopenia.
- Pregnancy hyperhomocysteinemia is associated with fetal developmental defects.
Purpose of the Study:
- To investigate the effects of maternal hyperhomocysteinemia on offspring bone volume.
- To examine changes in the epiphyseal growth plate of offspring from hyperhomocysteinemic mothers.
Main Methods:
- Adult female Sprague-Dawley rats were divided into control and experimental groups.
- The experimental group received homocysteine (100 mg/kg/day) in drinking water before and during pregnancy.
- Histomorphometric analysis of tibial, radial, and vertebral growth plates and bone volume fraction in newborn rat pups.
Main Results:
- Experimental dams exhibited significantly higher plasma homocysteine levels.
- Offspring of homocysteine-supplemented dams showed significantly decreased bone volume fraction in tibia, radius, and vertebra.
- The proliferative and hypertrophic zones of the growth plates were significantly increased in offspring from the experimental group.
Conclusions:
- Maternal homocysteine administration induces osteopenia in newborn rats.
- Hyperhomocysteinemia during pregnancy may disrupt normal epiphyseal cartilage development in rat embryos.
Abstract:
Severe hyperhomocysteinemia, as seen in classic homocystinuria, is associated with several skeletal malformations and osteopenia. Moreover, hyperhomocysteinemia during pregnancy has been associated with multiple developmental defects in the fetus. This study was undertaken to determine whether offspring of hyperhomocysteinemic mothers have demonstrable changes in bone volume and the epiphyseal growth plate. Ten adult female Sprague-Dawley rats were randomly assigned to the control or experimental group. The experimental group received 100 mg/kg/day of homocysteine in their drinking water for 3 weeks before mating and for the total duration of pregnancy. In each group, three pups per mother were randomly selected. The histomorphometric properties of tibial, radial and vertebral growth plates of newborn rats and the volume fraction of bone were compared between groups. The plasma homocysteine concentration at the end of study was significantly higher in dams in the experimental group (16.42+/-1.5 vs. 4.7+/-1.7 mumol/L, P<0.05). In offspring born to dams given the homocysteine supplement, the volume fraction of bone in the tibia (30.7+/-1.5% vs. 36.8+/-1.9%, P<0.05), radius (29.6+/-1.1% vs. 37.4+/-2%, P<0.05) and vertebra (34.4+/-1.8% vs. 41+/-1.9%, P<0.05) were significantly decreased whereas vertical heights of proliferative (423+/-25.1 vs. 301.8+/-28.1 microm for radius and 131.9+/-5.9 vs. 107.8+/-3.5 microm for vertebra) and hypertrophic zones (213.1+/-12 vs. 163.3+/-7.5 microm for tibia, 153.2+/-7.7 vs. 121.1+/-7.9 microm for radius and 112+/-9.9 vs. 88.4+/-10.1 microm for the vertebra) were increased (P<0.05). The results showed that the administration of homocysteine caused osteopenia in newborn rats. In addition, these data suggest that hyperhomocysteinemia may induce disruption of normal development of epiphyseal cartilage in the rat embryo.
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