A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Kandaswamy, Deivanayagam
- Identification TIMP-1 and TIMP-2 in Human Radicular Dentine - In Vitro Study
Authors
1 Department of Conservative Dentistry and Endodontics, Sri Ramachandra University, IN
Source
Journal of Academy of Dental Education, Vol 1, No 2 (2014), Pagination: 12-16Abstract
Aim: To identify TIMP – 1 and TIMP – 2 in human radicular dentine using confocal laser scanning microscopy. Materials and Methods: Thirty freshly extracted non carious human single ischolar_mained pre molars were obtained and stored in isotonic saline at -70°C prior to use. All the teeth were decoronated at the CEJ using a diamond. Teeth were divided into 2 groups (Group 1: TIMP-1 analysis n = 15; Group 2: TIMP-2 analysis n = 15). Teeth were sectioned using a hard tissue microtome, mounted and viewed under confocal laser scanning microscopy. Results: TIMP-1 and TIMP-2 were detected in radicular dentine and were seen to be distributed more towards the inner dentine layer closer to the pulp. Conclusion: Due to a shorter half life of TIMP-1 and 2 as compared to the MMP, there is a need to use MMP inhibitors prior to obturation of the ischolar_main canal.Keywords
Bond Degradation, Collagenolysis, Confocal Laser Scanning Microscopy, Matrix Metalloproteinase, Radicular Dentine, Tissue Inhibitors of Metalloproteinase.References
- Becher N, Hein M, Uldbjerg N, et al. Balance between Matrix Metalloproteinases (MMP) and Tissue Inhibitors of Metalloproteinases (TIMP) in the cervical mucus plug estimated by determination of free non-complexed TIMP. Reproductive Biology and Endocrinology. 2008; 6:223–32.
- Birkedal-Hansen H. Role of matrix metalloproteinases in human periodontal diseases. Journal of Periodontology. 1993; 64:474–84.
- Boff LL, Grossi ML, Prates LH, et al. Effect of the activation mode of post adhesive cementation on push-out bond strength to ischolar_main canal dentin. Quintessence International. 2007; 38:387–94.
- Breschi L, Mazzoni A, Ruggeri A, et al. Dental adhesion review: aging and stability of the bonded interface. Dental Materials. 2008; 24:90–101.
- Carrilho MR, Carvalho RM, de Goes MF, et al. Chlorhexidine preserves dentin bond in vitro. Journal of Dental Research. 2007; 86:90–4.
- Carrilho MR, Geraldeli S, Tay F, et al. In vivo preservation of the hybrid layer by chlorhexidine. Journal of Dental Research. 2007; 86:529–33.
- Carrilho MR, Tay FR, Pashley DH, et al. Mechanical stability of resin-dentin bond components. Dental Materials. 2005; 21:232–41.
- Demeule M, Brossard M, Pagé M, et al. Matrix metalloproteinase inhibition by green tea catechins. Biochimica et Biophysica Acta. 2000 Mar 16; 1478(1):51–60.
- Garbisa S, Sartor L, Biggin S, et al. Tumor gelatinases and invasion inhibited by the green tea flavanol epigallocatechin3-gallate. Cancer. 2001; 91:822–32.
- Geiger SB, Harper E. The inhibition of human gingival collagenase by an inhibitor extracted from human teeth. Journal of Periodontal Research. 1981; 16:8–12.
- Goldberg M, Smith AJ. Cells and extracellular matrixes of dentin and pulp: a biological basis for repair and tissue engineering. Critical Reviews in Oral Biology & Medicine. 2004; 15:13–27.
- Goldberg M, Septier D, Bourd K, et al. Immunohistochemical localization of MMP-2, MMP-9, TIMP-1, and TIMP-2 in the forming rat incisor. Connective Tissue Research. 2003; 44:143–53.
- Hall R, Septier D, Embery G, et al. Stromelysin-1 (MMP-3) in forming enamel and predentine in rat incisor-coordinated distribution with proteoglycans suggests a functional role. Histochemical Journal. 1999; 31:761–70.
- Hebling J, Pashley DH, Tjäderhane L. Chlorhexidine arrests subclinical degradation of dentin hybrid layers in vivo. Journal of Dental Research. 2005; 84:741–6.
- Hiraishi N, Yiu CK, King NM, et al. Effect of chlorhexidine incorporation into a self-etching primer on dentine bond strength of a luting cement. Journal of Dentistry. 2010; 38:496–502.
- Huang FM, Yang SF, Chang YC. Up-regulation of gelatinases and tissue type plasminogen activator by ischolar_main canal sealers in human osteoblastic cells. Journal of Endodontics. 2008; 34:291–4.
- Huet E, Cauchard JH, Berton A, et al. Inhibition of plasminmediated prostromelysin-1 activation by interaction of long chain unsaturated fatty acids with kringle 5. Biochemical Pharmacology. 2004; 67:643–54.
- Ishiguro K, Yamashita K, Nakagaki H, et al. Identification of tissue inhibitor of metalloproteinases-1 (TIMP-1) in human teeth and its distribution in cementum and dentine. Archives of Oral Biology. 1994; 39:345–9.
- Nowicki JB, Daniel S. An In Vitro Spectroscopic Analysis to Determine the Chemical Composition of the Precipitate Formed by Mixing Sodium Hypochlorite and Chlorhexidine. Journal of Endodontics. 2011; 37:983–8.
- Karjalainen S, Söderling E, Pelliniemi L, et al. Immunohistochemical localization of types I and III collagen and fibronectin in the dentine of carious human teeth. Archives of Oral Biology. 1986; 31:801–6.
- Kreis T, Vale R. Matrix metalloproteinases. In: Sternlicht MD, Werb Z, editors. Guidebook to extracellular matrix, anchor, and adhesion proteins, 2nd edn. San Francisco: Oxford University Press; 1999. p. 519–42.
- Kut C, Assoumou A, Dridi M, et al. Morphometric analysis of human gingival elastic fibres degradation by human leukocyte elastase protective effect of avocado and soybean unsaponifiables (ASU). Pathologie Biologie (Paris). 1998; 46:571–6.
- Leitune VC, Collares FM, Werner Samuel SM, Influence of chlorhexidine application at longitudinal push-out bond strength of fiber posts. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology. 2010; 110:77–81.
- Leonardi R, Loreto C, Immunohistochemical localization of tissue inhibitor of matrix metalloproteinase-1 (TIMP1) in human carious dentine. Acta Histochemica. 2010; 112:298–302.
- Martin-De Las Heras S, Valenzuela A, Overall CM. The matrix metalloproteinase gelatinase A in human dentine. Archives of Oral Biology. 2000; 45:757–65.
- Mazzoni A, Carrilho M, Papa V, et al. MMP-2 assay within the hybrid layer created by a two-step etch-and-rinse adhesive: biochemical and immunohistochemical analysis. Journal of Dentistry. 2011; 39:470–7.
- Mazzoni A, Mannello F, Tay FR, et al. Zymographic analysis and characterization of MMP-2 and -9 forms in human sound dentin. Journal of Dental Research. 2007; 86:436–40.
- Mazzoni A, Papa V, Nato F, et al. Immunohistochemical and biochemical assay of MMP-3 in human dentine. Journal of Dentistry. 2011; 39:231–7.
- Mazzoni A, Pashley DH, Nishitani Y, et al. Reactivation of inactivated endogenous proteolytic activities in phosphoric acid-etched dentine by etch-and-rinse adhesives. Biomaterials. 2006; 27:4470–6.
- Mazzoni A, Pashley DH, Tay FR, et al. Immunohistochemical identification of MMP-2 and MMP-9 in human dentin: correlative FEI-SEM/TEM analysis. Journal of Biomedical Materials Research Part A. 2009; 88:697–703.
- Nagase H, Woessner JF, Jr. Matrix metalloproteinases. The Journal of Biological Chemistry. 1999; 274:21491–4.
- Nuttall RK, Sampieri CL, Pennington CJ, et al. 2004. Expression analysis of the entire MMP and TIMP gene families during mouse tissue development. FEBS Letters. 563:129–34.
- Palosaari H, Pennington CJ, Larmas M. Expression profile of matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs in mature human odontoblasts and pulp tissue. European Journal of Oral Sciences. 2003; 111:117–27.
- Sa Y, Hao J, Samineni D, et al. Brain distribution and elimination of recombinant human TIMP-1 after cerebral ischemia and reperfusion in rats. Neurological Research. 2011; 33:433–8.
- Santos J, Carrilho M, Tervahartiala T, et al. Determination of matrix metalloproteinases in human radicular dentin. Journal of Endodontics. 2009; 35:686–9.
- Sartor L, Pezzato E, Dell'Aica I, Caniato R, et al. Inhibition of matrix-proteases by polyphenols: chemical insights for anti-inflammatory and anti-invasion drug design. Biochemical Pharmacology. 2002; 64:229–37.
- Sluijter JP, de Kleijn DP, Pasterkamp G. Vascular remodeling and protease inhibition--bench to bedside. Cardiovascular Research. 2006; 69:595–603.
- Sulkala M, Larmas M, Sorsa T, et al. The localization of matrix metalloproteinase-20 (MMP-20, enamelysin) in mature human teeth. Journal of Dental Research. 2002; 81:603–7.
- Tay FR, Pashley DH, Loushine RJ, et al. Self-etching adhesives increase collagenolytic activity in radicular dentin. Journal of Endodontics. 2006; 32:862–8.
- Tjaderhane L, Larjava H, Sorsa T, et al. The activation and function of host matrix metalloproteinases in dentin matrix breakdown in caries lesions. Journal of Dental Research, 1998; 77:1622–9.
- Tjaderhane L, Palosaari H, Wahlgren J, et al. Human odontoblast culture method: the expression of collagen and matrix metalloproteinases (MMPs). Advances in Dental Research. 2001; 15:55–8.
- Visse R, Nagase H. Matrix metalloproteinases and tissue inhibitors of metalloproteinases: structure, function and biochemistry. Circulation Research. 2003; 92:827–39.
- Woessner JF, Jr. Matrix metalloproteinases and their inhibitors in connective tissue remodeling. FASEB J. 1991; 5:2145–54.
- Yu WH, Yu S, Meng Q, et al, 2000. TIMP-3 binds to sulfated glycosaminoglycans of the extracellular matrix. The Journal of Biological Chemistry. 275:31226–32.
- An Invitro Comparison of Dissolution of Human Pulp in Sodium Hypochlorite, Ethanolic Extract and Digestive Secretion of Insectivorous Plants
Authors
1 Department of Conservative Dentistry and Endodontics, Sree Balaji Dental College and Hospital, Bharath Institute of Higher Education and Research, Narayanapuram, Pallikaranai, Chennai, Tamil Nadu, IN
2 Department of Conservative Dentistry & Endodontics, Sri Ramachandra University, Chennai, IN
3 Department of Conservative Dentistry & Endodontics, Best Dental College, Madurai, IN
4 Department of Conservative Dentistry & Endodontics, Madha Dental College, Chennai, IN
Source
Indian Journal of Public Health Research & Development, Vol 10, No 12 (2019), Pagination: 942-946Abstract
The tissue dissolution property of irrigating solutions is important for successful endodontic treatment. Sodium hypochlorite (NaOCl) is a well-known tissue dissolvent, but no data have been published on herbal alternative to NaOCl. The purpose of this study was to investigate the pulp tissue dissolution capacity of sodium hypochlorite, ethanolic extract of Drosera rotundifolia and digestive fluid of Nepenthes khasiana. Freshly extracted intact vital teeth, extracted for orthodontic and impaction reasons were collected and stored at – 20 ˚C. The pulp tissues were removed by splitting of the teeth when required.
Method: The pulp tissues were randomly divided into 4 groups (n = 10), individual sample was weighed 7 mg each. The groups were as follows, Group I: 5% NaOCl, Group II: digestive fluid of Nepenthes khasiana, Group III: Drosera rotundifolia (ethanolic extract), Group IV: distilled water. The test solutions were added to tubes containing tissue samples, the tissues were removed from the test solutions at 5, 15, 20, 30 min, 1,2,3,4,5,6,7 hr blotted dry with the tissue paper and weighed using precision balance.
Results: The results showed complete dissolution of pulp tissue in Group I at 20 minutes, Group II at 7 hr, Group III and IV showed no dissolution of pulp at the investigated time intervals.
Conclusion: The digestive fluid of Nepenthes khasiana could be considered as an herbal alternative to NaOCl for pulp tissue dissolution as it completely dissolved the pulp tissue similar to 5% NaOCl, but at different time intervals.