TY - JOUR
T1 - The effect of pulsed electromagnetic field exposure on fracture healing through the wnt signal pathway
AU - Umiatin, U.
AU - Dilogo, Ismail Hadisoebroto
AU - Sari, Puji
AU - Wijaya, Sastra Kusuma
N1 - Funding Information:
This study was supported by grant from Universitas 1309/UN2.R3.1/HKP.05.00/2018
Publisher Copyright:
© 2020 Umiatin U., Ismail Hadisoebroto Dilogo, Puji Sari and Sastra Kusuma Wijaya.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020
Y1 - 2020
N2 - Pulsed Electromagnetic Fields (PEMF) is reported to encourage the healing of nonunion fractures. However, the mechanism by which this occurs is still not known. Wnt signaling pathways are believed to be important signaling pathways in bone formation. This study will evaluate the healing of delayed union femur fracture, given PEMF exposure. 48 Spraque Dawley rats were fracturized at the left femoral shaft. These rats were randomized into two groups: A control group (24 rats) and the PEMF group (24 rats). The PEMF group was given PEMF exposure of 1.6 mT, with a frequency of 50 Hz for 4 h every day for 5, 10, 18 and 28 days, while the control group was not given PEMF exposure. Consequently, on days 5, 10, 18 and 28 days after fracture, 6 rats from each group were sacrificed. Callus bone was used for histological and RT-PCR examination on the expression of Wnt10b, Wnt5a and β-catenin. Blood samples were taken to examine Alkaline Phosphatase (ALP) activity using the ELISA method. Hematoxylin Eosin (HE) staining results showed that in the initial phase of healing, fibrous tissue in the fracture gap of the PEMF group was less compared to the control group. In the PEMF group, ALP activity increased significantly on day 10. This is thought to be related to an increase in osteoblast activity in a bone matrix formation. Furthermore, RT-PCR examination results showed that Wnt10b, Wnt5a and β-catenin gene expression was higher in the PEMF group compared to the control group. It can be concluded that PEMF exposure is thought to accelerate delayed union fracture healing through the Wnt signal pathway.
AB - Pulsed Electromagnetic Fields (PEMF) is reported to encourage the healing of nonunion fractures. However, the mechanism by which this occurs is still not known. Wnt signaling pathways are believed to be important signaling pathways in bone formation. This study will evaluate the healing of delayed union femur fracture, given PEMF exposure. 48 Spraque Dawley rats were fracturized at the left femoral shaft. These rats were randomized into two groups: A control group (24 rats) and the PEMF group (24 rats). The PEMF group was given PEMF exposure of 1.6 mT, with a frequency of 50 Hz for 4 h every day for 5, 10, 18 and 28 days, while the control group was not given PEMF exposure. Consequently, on days 5, 10, 18 and 28 days after fracture, 6 rats from each group were sacrificed. Callus bone was used for histological and RT-PCR examination on the expression of Wnt10b, Wnt5a and β-catenin. Blood samples were taken to examine Alkaline Phosphatase (ALP) activity using the ELISA method. Hematoxylin Eosin (HE) staining results showed that in the initial phase of healing, fibrous tissue in the fracture gap of the PEMF group was less compared to the control group. In the PEMF group, ALP activity increased significantly on day 10. This is thought to be related to an increase in osteoblast activity in a bone matrix formation. Furthermore, RT-PCR examination results showed that Wnt10b, Wnt5a and β-catenin gene expression was higher in the PEMF group compared to the control group. It can be concluded that PEMF exposure is thought to accelerate delayed union fracture healing through the Wnt signal pathway.
KW - Alkaline Phosphatase
KW - Delayed Union
KW - Fracture
KW - PEMF
KW - Wnt
UR - https://www.scopus.com/pages/publications/85098090679
U2 - 10.3844/ojbsci.2020.239.249
DO - 10.3844/ojbsci.2020.239.249
M3 - Article
AN - SCOPUS:85098090679
SN - 1608-4217
VL - 20
SP - 239
EP - 249
JO - OnLine Journal of Biological Sciences
JF - OnLine Journal of Biological Sciences
IS - 4
ER -