Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.1.3.1 (
alkaline phosphatase
)
47,916
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Osteopenia is characterized by bone loss and deterioration of trabecular bone, which leads to osteoporotic fractures. This disease is highly prevalent in industrialized areas and is associated with exposure to endocrine disrupting chemicals (EDCs).
Diisononyl phthalate
(
DINP
) is one of these EDCs and is mainly used as a plasticizer in flexible polyvinyl chloride (PVC) products. Although it is well known that exposure to
DINP
is harmful to humans, no studies have been reported concerning its contribution to osteopenia. Therefore, in this study, we injected
DINP
(2, 20, and 200mg/kg) into C3H/HeN mice for 6weeks and found that the uterus weight, bone (femur and tibia) weight, and bone length of the
DINP
-exposed mice were reduced compared to those of the SHAM group. On the other hand, body weight, the serum
alkaline phosphatase
(
ALP
) and inorganic phosphorus (IP) levels in the
DINP
treated mice were increased compared with those of the SHAM group. The tartrate-resistant acid phosphatase (TRAP) activity (bone resorption marker) was increased and the bone
alkaline phosphatase
(BALP) activity was lowered by the treatment with
DINP
as compared with the SHAM group. Furthermore, the microarchitecture of the femur and tibia in the intact mice was destroyed by the
DINP
injection. The tissue volume (TV), bone volume (BV), BV/TV, bone surface (BS), BS/TV, trabecular thickness (Tb.Th), and trabecular number (Tb.N) were reduced and the trabecular pattern factor (Tb.Pf), structure model index (SMI), and trabecular separation (Tb.Sp) were increased by the
DINP
injection. The bone mineral density (BMD) of the femur and tibia was lower in the
DINP
group than in the SHAM group. These results indicate that
DINP
contributes to an increased risk of osteopenia via destruction of the microarchitecture and enhancement of osteoclast activity.
...
PMID:Effects of diisononyl phthalate on osteopenia in intact mice. 2889 86