Effects of Fixation Delay and Colchicine on the Presence of Stippled Material in the Newly Formed Enamel of the Rat Incisor

1988 ◽  
Keyword(s):  
Rat Incisor ◽  
Fixation Delay

scholarly journals An Investigation of the Wild Rat Crown Incisor as an Indicator of Lead (Pb) Exposure Using Inductively Couple Plasma Mass Spectrometry (ICP-MS) and Laser Ablation ICP-MS

2021 ◽  
Vol 18 (2) ◽  
pp. 767
Author(s):  
Andrew Kataba ◽  
Shouta M. M. Nakayama ◽  
Hokuto Nakata ◽  
Haruya Toyomaki ◽  
Yared B. Yohannes ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Laser Ablation ◽  
Inductively Couple Plasma ◽  
Health Concern ◽  
Sprague Dawley ◽  
Rat Incisor ◽  
Sprague Dawley Rats ◽  
Icp Ms ◽  
Plasma Mass Spectrometry ◽  
Pb Exposure

Lead (Pb) is a metal toxicant of great public health concern. The present study investigated the applicability of the rat incisor in Pb exposure screening. The levels of lead in teeth (Pb-T) in the crown and root of incisors in laboratory Pb-exposed Sprague Dawley rats were quantified using inductively coupled plasma mass spectrometry (ICP-MS). The crown accumulated much Pb-T than the root of the Sprague Dawley rat incisor. The levels of lead in blood (Pb-B) were positively correlated with the Pb-T in the crown and root incisors of the Sprague Dawley rats. As an application of the Pb-T crown results in experimental rats, we subsequently analyzed the Pb-T in the crown incisors of Pb-exposed wild rats (Rattus rattus) sampled from residential sites within varying distances from an abandoned lead–zinc mine. The Pb-T accumulation in the crown of incisors of R. rattus rats decreased with increased distance away from the Pb–Zn mine. Furthermore, the Pb-T was strongly correlated (r = 0.85) with the Pb levels in the blood. Laser ablation ICP-MS Pb-T mappings revealed a homogenous distribution of Pb in the incisor with an increased intensity of Pb-T localized in the tip of the incisor crown bearing an enamel surface in both Sprague Dawley and R. rattus rats. These findings suggest that Pb-T in the crown incisor may be reflective of the rat’s environmental habitat, thus a possible indicator of Pb exposure.

Penetration of various molecular-weight proteins into the enamel organ and enamel of the rat incisor

1986 ◽  
Vol 31 (5) ◽  
pp. 287-296 ◽  
Author(s):  
M.D. McKee ◽  
B. Martineau-Doize ◽  
H. Warshawsky
Keyword(s):  
Molecular Weight ◽  
Enamel Organ ◽  
Rat Incisor

scholarly journals Cytochemical localization of calcium and Ca2+,Mg2(+)-adenosine triphosphatase in colchicine-altered rat incisor ameloblasts.

1990 ◽  
Vol 38 (10) ◽  
pp. 1469-1478 ◽  
Author(s):  
D R Eisenmann ◽  
A H Salama ◽  
A M Zaki ◽  
S H Ashrafi
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Adenosine Triphosphatase ◽  
Morphological Changes ◽  
Rat Incisor ◽  
Cytochemical Localization ◽  
Early Maturation ◽  
Transmission Electron ◽  
Maturation Stages ◽  
Secretory Transport

Colchicine is known to affect secretory, transport, and degradative functions of ameloblasts. The effects of colchicine on membrane-associated calcium and Ca2+,Mg2(+)-ATPase in secretory and maturation ameloblasts were investigated cytochemically. The pyroantimonate (PPA) method was used for localizing calcium and a modified Wachstein-Meisel medium was used to localize Ca2+,Mg2(+)-ATPase. Sections representing secretory and early maturation stages were examined by transmission electron microscopy. Morphological changes induced by colchicine included dislocated organelles and other well-established reactions to such anti-microtubule drugs. Calcium pyroantimonate (Ca-PA) deposits in most ameloblast types were markedly reduced, with the greater reduction occurring in those cells more severely altered morphologically. However, the cell membranes of both control and experimental smooth-ended maturation ameloblasts were essentially devoid of Ca-PA. The normal distribution and intensity of Ca2+,Mg2(+)-ATPase was not affected by colchicine. Because the observed reduction of membrane-associated calcium is apparently not mediated by Ca2+,Mg2(+)-ATPase in this case, other aspects of the calcium regulating system of ameloblasts are apparently targeted by colchicine.

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