Histochemical study of intestinal mucins after administration of silver nanoparticles in Sprague–Dawley rats

2009 ◽  
Vol 84 (1) ◽  
pp. 63-69 ◽  
Author(s):  
Gil Nam Jeong ◽  
Un Bock Jo ◽  
Hyeon Yeol Ryu ◽  
Yong Soon Kim ◽  
Kyung Seuk Song ◽  
...  
2013 ◽  
Vol 60 ◽  
pp. 297-301 ◽  
Author(s):  
R. Ebabe Elle ◽  
S. Gaillet ◽  
J. Vidé ◽  
C. Romain ◽  
C. Lauret ◽  
...  

Toxics ◽  
2013 ◽  
Vol 1 (1) ◽  
pp. 36-45 ◽  
Author(s):  
Hyun Cho ◽  
Jae Sung ◽  
Kyung Song ◽  
Jin Kim ◽  
Jun Ji ◽  
...  

2000 ◽  
Vol 350 (3) ◽  
pp. 805-814 ◽  
Author(s):  
Niclas G. KARLSSON ◽  
Fredrik J. OLSON ◽  
Per-Åke JOVALL ◽  
Ylva ANDERSCH ◽  
Lennart ENERBÄCK ◽  
...  

The sialylation of the oligosaccharides from small-intestinal mucins during a 13-day infectious cycle was studied in Sprague–Dawley rats with the parasite Nippostrongylus brasiliensis. Sialic acid analysis and release, permethylation and analysis by GC-MS of the sialylated oligosaccharides isolated from the ‘insoluble’ mucin complex revealed a relative decrease (4–7-fold) of N-glycolylneuraminic acid compared with N-acetylneuraminic acid just before parasite expulsion. Northern blots showed that this effect was due to the decreased expression of a hydroxylase converting CMP-N-acetylneuraminic acid into CMP-N-glycolylneuraminic acid. Analysis of other rat strains showed that this parasite infection also caused the same effect in these animals. Detailed analysis of infected Sprague–Dawley rats revealed four sialylated oligosaccharides not found in the uninfected animals. These new oligosaccharides were characterized in detail and all shown to contain the trisaccharide epitope NeuAc/NeuGcα2-3(GalNAcβ1-4)Galβ1 (where NeuGc is N-glycolyl neuraminic acid). This epitope is similar to the Sda- and Cad-type blood-group antigens and suggests that the infection causes the induction of a GalNAcβ1-4 glycosyltransferase. This model for an intestinal infection suggests that the glycosylation of intestinal mucins is a dynamic process being modulated by the expression of specific enzymes during an infection process.


2016 ◽  
Vol 17 (1) ◽  
Author(s):  
Joanna Seiffert ◽  
Alison Buckley ◽  
Bey Leo ◽  
Nicholas G. Martin ◽  
Jie Zhu ◽  
...  

2021 ◽  
Vol 09 ◽  
Author(s):  
Asra Parveen ◽  
Vijay kumar B. Malashetty ◽  
Sushruta Marla ◽  
Shanth Reddy ◽  
Sidramappa Sirsand ◽  
...  

Background: Silver nanoparticles have been widely used in the field of nanomedicine. A comprehensive understanding of their pharmacokinetics is crucial for proper risk assessment and safe biomedical applications. Objectives: The purpose of this study was to investigate the safety of silver nanoparticles by determining its potential toxicity following 28 days administration in Sprague Dawley rats. Method: The silver nanoparticles were administered by intravenous injection at the doses of 100, 200 and 500 µg/kg body weight for 28 consecutive days. Animals in the control group were received sterile water for injection. Each group consists of 10 male and 10 female rats. Results: No treatment related effects were seen in any of the parameters monitored in rats given 100, 200 and 500 µg/kg body weight/day of silver nanoparticles. Conclusion: The study proved that the use of up to 500 µg/kg body weight biosynthesized silver nanoparticles have no toxic effect in the target organs and found safe. However, the safety of the nanoparticles might be attributed to the covering of biological moieties on nanoparticles. Hence, the biofunctionalized nanoparticles can be safely used by selecting the required size and dose in medicines and drug delivery systems.


2008 ◽  
Vol 20 (6) ◽  
pp. 567-574 ◽  
Author(s):  
Jae Hyuck Sung ◽  
Jun Ho Ji ◽  
Jin Uk Yoon ◽  
Dae Seong Kim ◽  
Moon Yong Song ◽  
...  

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