TOX 2017 Magyar Toxikológusok Társasága Tudományos konferencia Bükfürdő, Október

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TOX 2017 Magyar Toxikológusok Társasága Tudományos konferencia Bükfürdő, Október 11-13. Histopathological evaluation of the teeth in regulatory studies: what are the needs and what can we learn from it Dr. med. vet. Matthias Rinke, FTA Pathologie, FIATP

Teeth represent not a standard protocol organ, not required by any guideline Considered as by-product when looked at slides of the nasal cavity Pathologists feel somewhat uncomfortable when gross lesions occur or teeth are target More focus on teeth due to increased investigation of anticancer compounds

Overview of the Presentation: 1. Introduction (Physiology/Anatomy/Histology) 2. Non-proliferative Lesions (Examples from ToxPath) 3. Proliferative Lesions (Terminology only)

Embryology: Teeth formed by unique series of reciprocal inductive phenomena occurring between odontogenic epithelium and mesenchymal cells of the dental papilla and dental follicle Crown formation: continuous process in rodent incisors: Inner dental epithelium induction of mesenchymal cells of dental papilla differentiation into odontoblasts dentin deposition reciprocal induction of inner dental epithelium differentiation into ameloblasts deposition of enamel Root formation: Molar roots formed by Hertwig s root sheath i.e.fusion of inner and outer dental epithelium

Formation of Ameloblast (A) and Odontoblast (O) Layers, Mouse, longitudinal A O

Formation of Ameloblast and Odontoblast layers, longitudinal cut, Rat O A

Base of upper incisor, transverse cut (rat) A O Courtesy of Dr. H. Ernst

Neck region of upper incisor, transverse cut, Rat Ameloblasts Enamel Dentin Odontoblasts Pulp Courtesy of Dr. H. Ernst

Rodents: Anatomy of the tooth Only permanent, no deciduous/temporary teeth 1 incisor / 3 molars per quadrant 2 (I1/1,M3/3) =16 Incisors: Continuous growth / wearing Renewal within 40 to 50 days (rats) 35 to 45 days (mice) Malocclusion or fracture of teeth may accelerate growth by a factor of 2-3!

Tooth substance composed of: Enamel: 1% organic material (glycoproteins), 99% inorganic material (hydroxyapatite crystals) Dentin: ~ 20% organic material (collagen,glycoproteins) ~ 80% inorganic material (hydroxyapatite) Mineral content of rat incisor (mg/g dry weight): Ca: 275, P: 140, Mg: 5.5, Na: 5.3, K: 2,6

Decalcification: EDTA (3 weeks +) Citric Formic Acid (2 weeks) Microwave (few days) Disadvantage: loss of calculus, loss of enamel, tissue shrinkage and artifacts, suboptimal staining if over decalcified - Plastic embedding - Precision cutting - Grinding methods Disadvantage: High costs

Routine trimming of the nasal cavity*?? * From: Brown R and JF Hardisty: Oral Cavity, Esophagus, and Stomach. In: Pathology of the Fischer Rat, Academic Press 1990

Routine trimming of the nasal cavity* Rat, 3-4 levels Rat, Level 1 Mouse, 3 levels Rat, Level 2 * From: Ruehl-Fehlert CI, B Kittel, G Morawietz et al.: Revised guides for organ sampling and trimming in rats and mice Part 1 A joint publication of the RITA and NACAD groups, Exp Toxicol Pathol. 2003 Sep; 55(2-3):91-106

Modified trimming of the nasal cavity / jaws Transverse Section Longitudinal Section Additionally, one transverse section through the 2nd incisor of the lower jaw possible

Modified trimming of the nasal cavity with incisors of the upper jaw * From: Kuijpers MHM et al. (1996): The rat incisor in toxicologic pathology. Tox Path 24, 346-360

A Bone B Vasculature C Periodontal Ligament D Ameloblasts E Enamel F Dentin G Odontoblasts H Pulp A B C D E F G H

Congenital lesions: Deviations from normal number or position, malocclusion Degenerative lesions: Ameloblast and odontoblast degeneration/necrosis Tooth resorption Attrition Inflammatory and vascular lesions: Periodontal disease, pulpitis, dental abscesses, fistulae Neoplastic lesions

Non-neoplastic Terms Degeneration Necrosis Periodontal pocket Dentin niches Dentin, decreased Dentin matrix alteration Fracture Resorption Denticle(s) Pulp concretion Cyst(s) Thrombus Actual INHAND Nomenclature Fossey S. et al. 2016, JTP 29, 3 (supplement)

Supernumerary tooth rat mouse Courtesy of Dr. H. Ernst

Root Resorption: perforation of dentine layer by inflammatory tissue Dental cyst rat mouse Courtesy of Dr. H. Ernst

Dental folds Intrapulpal denticles SGH Courtesy of Dr. H. Ernst

Example 1: Antiparasitic compound, 13 weeks Inlife observation: Accelerated growth of incisors Y-shaped growth Malocclusion or fracture of teeth may accelerate growth by factor of 2-3! Yellow color of teeth due to thin ironcontaining layer.

Example 1: Antiparasitic compound, rat, 13 weeks A B A. Normal appearance, upper jaw B. Proliferation of gingival epithelium and periodontal ligament, inflammation

Example 1: Antiparasitic compound A B A. Normal appearance of the gingiva and periodontal ligament, lower jaw B. Periodontal ligament proliferation, gingiva hyperplasia

Example 1: Antiparasitic compound A B A. Gingivitis and hyperplasia B. Periodontal ligament proliferation, multifocal karyomegaly in cementoblast layer

Example 1: Antiparasitic compound B A B C A. Normal appearance of ameloblast layer, mid part B/C. Atrophy and degeneration of ameloblast layer

Example 1: Antiparasitic compound, transverse, lower jaw Control Control Mid Dose High Dose A B C D

Example 2: Anticancer compound 1, rat, 4 weeks Inlife Observation: Accelerated growth of incisors, fractures A B A. Normal appearance B. Degeneration of odontoblasts and dentin matrix alteration

Example 2: A B C A. Normal appearance B/C. Degeneration of odontoblasts and dentin matrix alteration with pulp concretions (pulp stones)

Example 2: Anticancer compound 1 A B A. Cystic lacunae formation within dentin, close to basis of incisor B. Accelarated growth, cellular remnants in normally acellular dentin

Example 2: Anticancer compound 1 A B C A. Normal Appearance B. Penetration of periodontal ligament into dentin (Tooth resorption) C. Fracture of cementum

Example 3: Anticancer compound 2, mouse, 13 weeks Inlife observation: Deformation and fracture of incisors A B C A. Altered dentin composition, hyperdentinosis B. Altered dentin, periodontal ligament and cementum within normal range C. Altered dentin, odontoblast and ameloblast layer without alterations

Example 3: Anticancer compound 2, mouse, 13 weeks Inlife observation: Deformation and fracture of incisors A B A./B. Fracture and pulp necrosis Attention: Septicemia possible

Example 4: Anticancer compound 3, rat, 13 weeks Inlife observation: Discoloration and occasional fracture of incisors A A./B. Fracture and pulp necrosis, Necrosis of ameloblast layer B

Example 4: Anticancer compound 3, rat, 13 weeks Early changes of ameloblast layer vacuolization

Example 4: Anticancer compound 3, rat, 13 weeks Enamel defects and dentin matrix alterations

Example 4: Anticancer compound 3, rat, 13 weeks Degeneration of periodontal ligament

Example 4: Anticancer compound 3, rat, 13 weeks Severe vascular degeneration of dental growth zone

Example 4: Anticancer compound 3, rat, 13 weeks Degeneration of odontoblast layer and protrusion into dentin

Example 4: Anticancer compound 3, rat, 13 weeks Sequestration and production of dentin (denticles?) within pulp cavity

Example 4: Anticancer compound 3, rat, 13 weeks Early fractures with necrosis

Example 5: Anticancer compound 4, rat, 3d on 3d off 3d on A B A. Necrosis of odontoblast layer at basis of odontogenic epithelium, d 3 B. Regeneration of odontoblast layer during drug holiday, d 6

Example 5: Anticancer compound 4, rat, 3d on 3d off 3d on A B A. Odontoblast degeneration, B. Pulp necrosis, loss of dentin

Example 5: Anticancer compound 4, rat, 3d on 3d off 3d on A B A./B. Odontoblast degeneration and sequestration of dentin

Actual INHAND Nomenclature Fossey S. et al. 2016, JTP 29, 3 (supplement) Neoplastic Terms Ameloblastoma (TgAC) Ameloblastic odontoma Odontogenic fibroma Odontoma (no tumor/hamartoma) Cementifying/ossifying fibroma Tumor, odontogenic, benign Tumor, odontogenic, malignant

What about Non-rodents and Relevance of Rodent Findings for Humans?

Dentition in Beagle dogs Deciduous Teeth Permanent Teeth Eruption on day Exfoliation on day Eruption on day Incisors 23 25 (+/- 3) 114-133 (+/- 6) 115 133 (+/- 6) Canines 21 22 (+/- 2) 140 160 (+/- 23) 146 (+/- 7) Premolars - - I:106 (+/- 8) II-IV: 136 155 (+/- 6) Molars 29 35 (+/- 4) 137 155 (+/- 7) 128 175 (+/- 7)

Beagle dog: Trimming of the teeth / Upper jaw Transverse Section Longitudinal Section

Example 6: Anticancer compound Beagle Dog, Age at study start 119-147 days, 4 wk + 4 wk Recovery Inlife Observations: none A B A. Control, incisor, normal appearance, straight dentinal canaliculi B. Treated, incisor, altered dentin composition

Example 6: Anticancer compound, dog A B A. Treated, incisor, base of tooth with altered dentin matrix (4 wk) B. Treated, progressed dentinal alteration, followed by normal growth (4 wk R)

Example 6: Anticancer compound, Beagle dog, 1 year Inlife observation: persisting canines A B A. Control, incisor, normal appearance B. Treated, incisor, more or less normal, straight dentinal canaliculi

Example 6: Anticancer Compound 2, Beagle Dog, 1 year A B A. Treated, found dead on day 232, incisor, undulated dentinal canaliculi B. Treated, same animal, canine tooth, altered dentin composition

Known reasons for incisor lesions: Hypovitaminosis A Hypovitaminosis D Hypovitaminosis E Hypervitaminosis D Increased thickness of enamel covered dentin Reduced thickness of cementum-covered dentin Pulp invasion by odontogenic epithelium Wide zone of predentin, marbled dentin hypocalcified cementum Degeneration of enamel and fibrous replacement Hypercalcified dentin and cementum Ossification of periodontal membranes

Known reasons for incisor lesions: Ca and P Deficiency Mg Deficiency Fluorosis Tetracyclines Doxorubicin Adriamycin Cyclophosphamide VEGF Inhibitors Tubulin Inhibitors Wide zone of predentin Vascular inclusions in dentin Disturbed dentin calcification (stratification) Enamel atrophy and hypoplasia Disturbed dentin calcification Enamel hypoplasia Enamel defects Necrosis of pulp mesenchyme and odontoblasts Necrosis of pulp mesenchyme and odontoblasts Growth interruption, supernumerary teeth Degeneration/necrosis of odontoblasts Enamel hypoplasia and discoloration

Rodent: Conclusions Unique model of dental pathological processes Continuous growth and differentiation Odontogenic tissue remains functional during life span Sensitive recorder of altered mineral metabolism Modify level 1 of the nasal cavity slide Additional use of longitudinal cuts of the incisor of lower jaw is proposed

Dog: Conclusions Sensitive recorder of altered mineral metabolism Incisor teeth are easy to process Always think of age of the animals and duration of study, renewal of the tooth takes some time

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