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1.
Chinese journal of integrative medicine ; (12): 830-834, 2018.
Article in English | WPRIM | ID: wpr-687925

ABSTRACT

<p><b>OBJECTIVE</b>To observe wet cupping therapy (WCT) on local blood perfusion and analgesic effects in patients with nerve-root type cervical spondylosis (NT-CS).</p><p><b>METHODS</b>Fifty-seven NT-CS patients were randomly divided into WCT group and Jiaji acupoint-acupuncture (JA) group according a random number table. WCT group (30 cases) was treated with WCT for 10 min, and JA group (27 cases) was treated with acupuncture for 10 min. The treatment efficacies were evaluated with a Visual Analogue Scale (VAS). Blood perfusion at Dazhui (GV 14) and Jianjing (GB 21) acupoints (affected side) was observed with a laser speckle flowmetry, and its variations before and after treatment in both groups were compared as well.</p><p><b>RESULTS</b>In both groups, the VAS scores significantly decreased after the intervention (P<0.01), while the blood perfusion at the two acupoints significantly increased after intervention (P<0.05); however, the increasement magnitude caused by WCT was obvious compared with JA (P<0.05).</p><p><b>CONCLUSIONS</b>WCT could improve analgesic effects in patients with NT-CS, which might be related to increasing local blood perfusion of acupunct points.</p>

2.
Biomedical and Environmental Sciences ; (12): 453-456, 2016.
Article in English | WPRIM | ID: wpr-258800

ABSTRACT

The use of exogenous carbon monoxide releasing molecules (CORMs) provides promise for clinical application; however, the hazard potential of CORMs in vivo remains poorly understood. The developmental toxicity of CORM-3 was investigated by exposure to concentrations ranging from 6.25 to 400 μmol/L during 4-144 h post fertilization. Toxicity endpoints of mortality, spontaneous movement, heart rate, hatching rate, malformation, body length, and larval behavior were measured. CORM-3 disrupted the progression of zebrafish larval development at concentrations exceeding 50 μmol/L, resulting in embryonic developmental toxicity.


Subject(s)
Animals , Carbon Monoxide , Pharmacology , Cardiotonic Agents , Toxicity , Dose-Response Relationship, Drug , Embryo, Nonmammalian , Embryonic Development , Organometallic Compounds , Toxicity , Zebrafish , Embryology , Metabolism
3.
Acta Pharmaceutica Sinica ; (12): 1677-1687, 2013.
Article in Chinese | WPRIM | ID: wpr-298026

ABSTRACT

Carbon monoxide has been proved to be an important signal molecule in body. Transition metal carbonyl compounds are solidified form of carbon monoxide. Numerous studies have shown that Ruthenium carbonyl carbon monoxide releasing molecules have a strong pharmacological activity. In this paper, five Ruthenium (II) carbonyl CORMs 1-5 were synthesized and their toxicology, tissue distribution and interaction with blood endogenous substances were investigated. The results showed CORMs' IC50 to fibroblasts are ranged from 212.9 to 2089.2 micromol x L(-1). Their oral LD50 to mouse is between 800 to 1600 mg x kg(-1). After repeated administration, CORMs 1 and CORMs 5 haven't shown an obvious influence to rats' liver and kidney function, but caused the injury to liver and kidney cells. The in vivo distribution result revealed the majority of CORMs were distributed in blood, liver and kidney, only a small part of CORMs distributed in lung, heart and spleen. They could scarcely cross the blood-brain barrier and distribute to brain. The non-CO ligands in structure have an obvious relevance to their in vivo absorption and distribution. Interestingly, CORMs could enhance the fluorescence of bovine serum albumin, and this enhancement was in direct proportion with the concentration of CORMs. Under different conditions, interaction of CORMs with glutathione got different type of products, one is Ruthenium (II) tricarbonyl complexes, and Ruthenium (II) dicarbonyl complexes.


Subject(s)
Animals , Mice , Rats , Carbon Monoxide , Chemistry , Pharmacokinetics , Toxicity , Fibroblasts , Kidney , Liver , Molecular Structure , Organometallic Compounds , Chemistry , Pharmacokinetics , Toxicity , Rats, Wistar , Ruthenium , Chemistry , Pharmacokinetics , Toxicity , Tissue Distribution
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