Document Detail

Cinnabar is Different from Mercuric Chloride in Mercury Absorption and Influence on the Brain Serotonin Level.
MedLine Citation:
PMID:  23302034     Owner:  NLM     Status:  Publisher    
The toxicity of cinnabar, a naturally occurring mercury sulfide (HgS), has long been referred to soluble mercury chloride (HgCl(2) ). To investigate whether the speciation of mercury plays a role in its disposition and toxicity, we hereby investigated and compared cinnabar with soluble HgCl(2) and pure insoluble HgS in mice on mercury absorption, tissue distribution and in relation to the biological effects. The male C57BL/6J mice were treated by oral administration of various doses of cinnabar, with 0.01 g/kg of HgCl(2) for comparison, or the same dose of cinnabar or pure HgS (0.1 g/kg), once a day for 10 consecutive days. The total mercury contents in serum, and tissue (brain, kidney, liver) were measured by atomic fluorescence spectrometer (AFS). The biological effects investigated involved monoamine neurotransmitters (serotonin, 5-HT) in brain as an indicator of therapeutic function, and serum alanine transaminase(ALT)as a marker of hepatic damage, blood urea nitrogen (BUN) and serum creatinine as markers for renal function. The mercury absorption of cinnabar or HgS was much less than that of HgCl(2) . The mercury levels in brains of the cinnabar group were only slightly changed and kept in a steady-state with the dose elevated. Cinnabar or HgS suppressed brain 5-HT levels. HgCl(2) could not cause any changes in brain 5-HT although the mercury level increased considerably. The results revealed that cinnabar or HgS is markedly different from HgCl(2) in mercury absorption, tissue distribution and influence on brain 5-HT levels, which suggests that the pharmacological and/or toxicological effects of cinnabar undertake other pathways from mercuric ions.
Qi Wang; Xiaoda Yang; Baoxu Zhang; Xiuwei Yang; Kui Wang
Related Documents :
7416554 - A preclinical study of eo-122, a new lidocaine-like antiarrhythmic drug.
23247044 - Evaluation of micronuclei in mice bone marrow and antioxidant systems in erythrocytes e...
11880574 - Oral administration of arabinogalactan affects immune status and fecal microbial popula...
7109024 - Pharmacokinetics of sulphadimidine in normal and febrile dogs.
23195604 - Plant regeneration from cultured disc florets of tagetes erecta l.
8619024 - The kinetics of repair of sublethal radiation-induced damage in pig skin: studies with ...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2013-1-10
Journal Detail:
Title:  Basic & clinical pharmacology & toxicology     Volume:  -     ISSN:  1742-7843     ISO Abbreviation:  Basic Clin. Pharmacol. Toxicol.     Publication Date:  2013 Jan 
Date Detail:
Created Date:  2013-1-10     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101208422     Medline TA:  Basic Clin Pharmacol Toxicol     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
© 2013 The Authors Basic & Clinical Pharmacology & Toxicology © 2013 Nordic Pharmacological Society.
Department of Toxicology, School of Public Health, Peking University.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  The complementary role of music therapy in the detection of awareness in disorders of consciousness:...
Next Document:  Gender-Specific Association of the Interleukin 18 Gene with Symptomatic Gallstone Disease.