Some cardiovascular effects of inorganic arsenic exposure in children exposed to drinking water

Author(s):  
C Osorio-Yáñez ◽  
A Barrera-Hernández ◽  
E Hernández-Castellanos ◽  
L Sánchez-Peña ◽  
A De Vizcaya-Ruiz ◽  
...  
Author(s):  
Xiaojuan Guo ◽  
Yoshihisa Fujino ◽  
Xiaolei Ye ◽  
Jun Liu ◽  
Takesumi Yoshimura

Molecules ◽  
2020 ◽  
Vol 25 (13) ◽  
pp. 3057
Author(s):  
Chang-Mu Chen ◽  
Min-Ni Chung ◽  
Chen-Yuan Chiu ◽  
Shing-Hwa Liu ◽  
Kuo-Cheng Lan

Arsenic is a toxic metalloid. Infants with a low birth-weight have been observed in areas with high-level arsenic in drinking water ranging from 463 to 1025 μg/L. A distal muscular atrophy side effect has been observed in acute promyelocytic leukemia patients treated with arsenic trioxide (As2O3) for therapy. The potential of As2O3 on muscle atrophy remains to be clarified. In this study, the myoatrophic effect of arsenic was evaluated in normal mice and sciatic nerve denervated mice exposed with or without As2O3 (0.05 and 0.5 ppm) in drinking water for 4 weeks. We found that both 0.05 and 0.5 ppm As2O3 increased the fasting plasma glucose level; but only 0.5 ppm arsenic exposure significantly decreased muscle mass, muscle endurance, and cross-sectional area of muscle fibers, and increased muscle Atrogin-1 protein expression in the normal mice. Both 0.05 and 0.5 ppm As2O3 also significantly enhanced the inhibitory effects on muscle endurance, muscle mass, and cross-sectional area of muscle fibers, and increased the effect on muscle Atrogin-1 protein expression in the denervated mice. These in vivo results suggest that inorganic arsenic at doses relevant to humans may possess myoatrophic potential.


AMBIO ◽  
2007 ◽  
Vol 36 (1) ◽  
pp. 82-84 ◽  
Author(s):  
Chin-Hsiao Tseng ◽  
Choon-Khim Chong ◽  
Ching-Ping Tseng ◽  
Jose A. Centeno

2021 ◽  
Vol 22 (18) ◽  
pp. 10077
Author(s):  
Manisha Thakur ◽  
Mahesh Rachamalla ◽  
Som Niyogi ◽  
Ashok Kumar Datusalia ◽  
Swaran Jeet Singh Flora

Arsenic is a key environmental toxicant having significant impacts on human health. Millions of people in developing countries such as Bangladesh, Mexico, Taiwan, and India are affected by arsenic contamination through groundwater. Environmental contamination of arsenic leads to leads to various types of cancers, coronary and neurological ailments in human. There are several sources of arsenic exposure such as drinking water, diet, wood preservatives, smoking, air and cosmetics, while, drinking water is the most explored route. Inorganic arsenic exhibits higher levels of toxicity compared its organic forms. Exposure to inorganic arsenic is known to cause major neurological effects such as cytotoxicity, chromosomal aberration, damage to cellular DNA and genotoxicity. On the other hand, long-term exposure to arsenic may cause neurobehavioral effects in the juvenile stage, which may have detrimental effects in the later stages of life. Thus, it is important to understand the toxicology and underlying molecular mechanism of arsenic which will help to mitigate its detrimental effects. The present review focuses on the epidemiology, and the toxic mechanisms responsible for arsenic induced neurobehavioral diseases, including strategies for its management from water, community and household premises. The review also provides a critical analysis of epigenetic and transgenerational modifications, mitochondrial oxidative stress, molecular mechanisms of arsenic-induced oxidative stress, and neuronal dysfunction.


2021 ◽  
pp. 096032712110459
Author(s):  
Macario Martínez-Castillo ◽  
Eliud A García-Montalvo ◽  
Mónica G Arellano-Mendoza ◽  
Luz del C Sánchez-Peña ◽  
Luis E Soria Jasso ◽  
...  

Inorganic arsenic (iAs) exposure is a serious health problem that affects more than 140 million individuals worldwide, mainly, through contaminated drinking water. Acute iAs poisoning produces several symptoms such as nausea, vomiting, abdominal pain, and severe diarrhea, whereas prolonged iAs exposure increased the risk of several malignant disorders such as lung, urinary tract, and skin tumors. Another sensitive endpoint less described of chronic iAs exposure are the non-malignant health effects in hepatic, endocrine, renal, neurological, hematological, immune, and cardiovascular systems. The present review outlines epidemiology evidence and possible molecular mechanisms associated with iAs-toxicity in several non-carcinogenic disorders.


2014 ◽  
Vol 31 (2) ◽  
pp. 154-162 ◽  
Author(s):  
Olusegun K. Afolabi ◽  
Adedoja D. Wusu ◽  
Olufunmilayo O. Ogunrinola ◽  
Esther O. Abam ◽  
David O. Babayemi ◽  
...  

2010 ◽  
Vol 29 (3) ◽  
pp. 291-296 ◽  
Author(s):  
Erik J. Tokar ◽  
Bhalchandra A. Diwan ◽  
Michael P. Waalkes

To expand our knowledge on the transplacental carcinogenic potential of inorganic arsenic, pregnant Tg.AC mice received drinking water with 0, 42.5, or 85 ppm arsenite from gestation day 8 to 18. After birth, groups (n = 25) of offspring received topical 12- O-tetradecanoyl phorbol-13-acetate (TPA) (2 μg twice a week) for 36 weeks and were killed; nonskin tumors were assessed. Arsenic increased adrenal cortical adenomas (ACAs; 25%-29%) compared with control (0%) independent of TPA in all male groups. Arsenic increased urinary bladder (UB) hyperplasia in males, but only with TPA. Arsenic induced ACAs in all female groups (control 0%; arsenic 17%-26%). Arsenic-treated females had UB hyperplasia in most groups (control 0%; arsenic 26%-32%), with 2 UB papillomas. All arsenic-treated females had uterine hyperplasia (26%-40%; control 4%) independent of TPA, and 3 had uterine tumors. Thus, arsenic in utero rapidly induces ACAs and uterine and UB preneoplasias in Tg.AC mice, showing transplacental carcinogenic potential in yet another strain of mice.


2019 ◽  
Vol 668 ◽  
pp. 310-317 ◽  
Author(s):  
Zhuo Zuo ◽  
Zhiyuan Liu ◽  
Tianchang Gao ◽  
Yuanyuan Yin ◽  
Zhendi Wang ◽  
...  

2006 ◽  
Vol 25 (S1) ◽  
pp. 73-73
Author(s):  
Xiaojuan Guo ◽  
Yoshihisa Fujino ◽  
Xiaolei Ye ◽  
Jun Liu ◽  
Takesumi Yoshimura

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