Volume 34, Issue 3 (May & June 2026)                   J Adv Med Biomed Res 2026, 34(3): 261-268 | Back to browse issues page

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Hussein A A M, Kadhim E F. Histological evaluation of the effect of local application of angiopoietin 1 on tooth development in rats on days 16. J Adv Med Biomed Res 2026; 34 (3) :261-268
URL: http://journal.zums.ac.ir/article-1-7931-en.html
1- College Of Dentistry, University Of Al-Ameed, kerbala, Iraq , alhusain@alameed.edu.iq
2- College Of Dentistry, University Of Baghdad, Baghdad, Iraq
Abstract:   (361 Views)
Background & Objective:  Angiopoietin-1 (Ang-1) is a key regulator of angiogenesis and vascular maturation and may play an important role in tooth development. This histological study aimed to evaluate the effect of the local application of angiopoietin-1 on tooth development in the upper molar region of neonatal rats at postnatal day 16.
 Materials & Methods:  Twelve neonatal rats weighing 3.5–4.0 g were maintained under controlled environmental conditions with free access to food and water. The animals were randomly allocated to either an experimental group (n = 6) or a control group (n = 6). The experimental group received a local injection of 10 μL of angiopoietin-1 into the upper right molar region, whereas the control group received an equal volume of sterile saline. All animals were sacrificed on postnatal day 16, and histological analyses were performed to evaluate tooth development.
Results:  Local administration of angiopoietin-1 significantly accelerated tooth development in all animals of the experimental group. Histological examination demonstrated enhanced deposition of dental hard tissues, characterized by increased dentin and enamel thickness, together with significantly higher numbers of odontoblasts, fibroblasts, and blood vessels compared with the control group. All evaluated histological parameters differed significantly between the two groups (P < 0.05).
Conclusion:  Local application of angiopoietin-1 promoted and accelerated tooth development in neonatal rats, suggesting that angiopoietin-1 may enhance odontogenesis by stimulating angiogenesis and promoting the formation and maturation of dental tissues.

 
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Type of Study: Original Research Article | Subject: Life Science
Received: 2026/02/7 | Accepted: 2026/06/2 | Published: 2026/06/29

References
1. Natiq N, Al-Hijazi AY. The effect of thymosin beta 4 on developing dental tissue (experimental study on rats). J Bagh Coll Dent.2016;28(3):69-74 [DOI:10.12816/0031111]
2. Kumar GS. ORBAN'S Oral Histology and Embryology. Fourteenth Edition, Tiruchengode, Tamil Nadu, INDIA 2015.
3. Chiego DJ. Essentials of Oral Histology and Embryology: A Clinical Approach, fifth ed, Elsevier, St. Louis, Missouri, 2019.
4. Pispa J, Thesleff I. Mechanisms of ectodermal organogenesis. Dev Biol.2003; 262(2): 195-205. [DOI:10.1016/S0012-1606(03)00325-7] [PMID]
5. Ali S, Farooq I, Khurram SA. Tooth development.An illustrated guide to oral histology 2021;1-13 [DOI:10.1002/9781119669616.ch1]
6. Chung AS, Ferrara N. Developmental and pathological angiogenesis. Annu Rev Cell Dev Biol.2011; 27: 563-84. [DOI:10.1146/annurev-cellbio-092910-154002] [PMID]
7. Steiniger B , Bubel, Werner Böckler S, Lampp K, Seiler A, Jablonski B, et al. Immunostaining of pulpal nerve fiber bundle/arteriole associations in ground serial sections of whole human teeth embedded in technovit (R) 9100. Cells Tissues Organs. 2013; 198(1): 57-65. [DOI:10.1159/000351608] [PMID]
8. Shadad, O, Chaulagain, R, Luukko, K Kettunen P. Establishment of tooth blood supply and innervation is developmentally regulated and takes place through differential patterning processes. J Anat.2019;234(4):465-79 [DOI:10.1111/joa.12950] [PMID] [PMCID]
9. Thesleff I, Mikkola M. The role of growth factors in tooth development. Int Rev Cytol. 2002;217: 93-135. [DOI:10.1016/S0074-7696(02)17013-6] [PMID]
10. Gomez‐Sosa JF, Caviedes‐Bucheli J, Diaz‐Barrera LE, Munoz HR. Gene expression of growth factors with angiogenic potential in human dental pulp from teeth with complete and incomplete root development. Int Endod J.2019;52(12):1716-22 [DOI:10.1111/iej.13188] [PMID]
11. Suri C, Jones PF, Patan S, Bartunkova S, Maisonpierre PC, Davis S, et al. Requisite role of angiopoietin-1, a ligand for the TIE2 receptor, during embryonic angiogenesis. Cell. 1996;87(7): 1171-80. [DOI:10.1016/S0092-8674(00)81813-9] [PMID]
12. Brindle NPJ. Signaling and functions of angiopoietin-1 in vascular protection. Circ Res. 2006; 98(8): 1014-23. [DOI:10.1161/01.RES.0000218275.54089.12] [PMID] [PMCID]
13. Griffioen AW. Angiogenesis. Encyclopedia of Cancer. 2011; 185-86. [DOI:10.1007/978-3-642-16483-5_274]
14. Caviedes-Bucheli J, Lopez-Moncayo LF, Muñoz-Alvear HD, Hernandez-Acosta F, Pantoja-Mora M, Rodriguez-Guerrero AS,et al. Expression of early angiogenesis indicators in mature versus immature teeth. BMC Oral Health.2020; 20(1):324 [DOI:10.1186/s12903-020-01313-1] [PMID] [PMCID]
15. N.P.J. Brindle, Signaling and functions of angiopoietin-1 in vascular protection. Circ Res.2006; 98(8): 1014-23. [DOI:10.1161/01.RES.0000218275.54089.12] [PMID] [PMCID]
16. Moxon JV, Trollope AF, Dewdney B, de Hollander C, Nastasi, Maguire D, et al.The effect of angiopoietin-1 upregulation on the outcome of acute ischaemic stroke in rodent models: A meta-analysis. J Cereb Blood Flow Metab.2019;39(12):2343-54 [DOI:10.1177/0271678X19876876] [PMID] [PMCID]
17. Kawamura K, Takahashi T, Kanazawa M, Igarashi H, Nakada, T, Nishizawa M, et al.. Effects of angiopoietin-1 on hemorrhagic transformation and cerebral edema after tissue plasminogen activator treatment for ischemic stroke in rats. PLoS ONE.2014; 9(6):e98639. [DOI:10.1371/journal.pone.0098639] [PMID] [PMCID]
18. Gutbier B, Neuhauß AK, Reppe, K, Ehrler C, Santel A, Kaufmann J,et al. Prognostic and pathogenic role of angiopoietin-1 and -2 in pneumonia. Am J Respir Crit Care Med.2018; 198(2): 220-31. [DOI:10.1164/rccm.201708-1733OC] [PMID]
19. Baqer RG, Abdullah B. Immunohistochemical expression of MMP2, VEGF and D2-40 as biological markers of local invasion potential, angiogenesis and lymphangiogenesis in oral squamous cell carcinoma and verrucous carcinoma. J Bagh Coll Dent.2016; 28(3): 59-64. [DOI:10.12816/0031109]
20. Al-Agele A ,Ghani J,Abdulghani B. In vivo histological evaluation of effect of direct pulp capping with BMP7 with and without laser therapy. J Pharm Sci Res. 2019;11: 2295-2301.
21. Dewi N, Syaify A, Wahyudi I. The enamel thickness of gestational diabetes mellitus rat off spring. J Dent Maxillofac Sci. 2021; 6,(3): 193-96 [DOI:10.15562/jdmfs.v6i3.1130]
22. Prasanth T, Saraswathi Tr. Histopathological and radiographic evaluation of rat molar teeth after traumatic injury-a pilot study. J Oral Maxillofac Pathol.2012; 16:313-17. [DOI:10.4103/0973-029X.102473] [PMID] [PMCID]
23. Fadhil E, Alhijazi AY. Histological and immunohistochemical evaluation of the effect of local exogenous application of VEGF on bone healing (experimental study in rat). J Bagh Coll Dent.2014; 26 :108-115. [DOI:10.12816/0015148]

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