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1.
Mycopathologia ; 182(7-8): 715-720, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28154954

ABSTRACT

We report a 66-year-old female patient with deep dermatophytosis caused by zoophilic strain of Trichophyton interdigitale, a rare granulomatous presentation of Trichophyton species infection in patients with underlying systemic diseases, and she was successfully cured by itraconazole. Since the identification of Trichophyton mentagrophytes complex had been misused for years, a brief discussion of molecular diagnosis and taxonomy of T. mentagrophytes complex is given. The pathogenesis and comparison with cases reported in the literature are also discussed.


Subject(s)
Antifungal Agents/administration & dosage , Itraconazole/administration & dosage , Tinea/diagnosis , Tinea/drug therapy , Trichophyton/isolation & purification , Aged , Female , Humans , Tinea/microbiology , Treatment Outcome , Trichophyton/classification , Trichophyton/genetics
2.
J Agric Food Chem ; 57(6): 2206-10, 2009 Mar 25.
Article in English | MEDLINE | ID: mdl-19219995

ABSTRACT

Diabetic nephropathy progressed to end-stage renal disease (ESRD) is found in type 1 or type 2 diabetes. Oxidative stress is one of the precipitation factors in diabetic nephropathy. Previously, Hibiscus sabdariffa Linnaeus and its polyphenol extracts were found to possess antioxidative effects. This study is aimed to investigate the effect of Hibiscus sabdariffa L. polyphenol extract (HPE) in streptozotocin (STZ) induced diabetic nephropathy. The results show that HPE reduced kidney mass induced by STZ significantly, as well as improving hydropic change of renal proximal convoluted tubules in the rats. HPE also significantly reduced serum triglyceride, total cholesterol and LDL in STZ induced rats. Treatment with HPE significantly increased the activity of catalase and glutathione and reduced lipid peroxidation (thiobarbituric acid-reactive substances, TBARS). The findings of this research show the beneficial effects of HPE on STZ induced diabetic nephropathy including pathology, serum lipid profile and oxidative marker in kidney.


Subject(s)
Diabetes Mellitus, Experimental/drug therapy , Diabetes Mellitus, Type 1/drug therapy , Diabetic Nephropathies/drug therapy , Flavonoids/administration & dosage , Hibiscus/chemistry , Phenols/administration & dosage , Plant Extracts/administration & dosage , Animals , Antioxidants/administration & dosage , Diabetic Nephropathies/pathology , Lipids/blood , Male , Organ Size , Polyphenols , Rats , Rats, Sprague-Dawley
3.
Biosci Biotechnol Biochem ; 73(2): 385-90, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19202285

ABSTRACT

Oxidative stress and inflammation are related to several chronic diseases including cancer and atherosclerosis. Hibiscus sabdariffa Linnaeus has been found to possess antioxidant effects. In this study, polyphenols extracted from Hibiscus sabdariffa L. (HPE) were used to detect anti-inflammatory effects on nitrite and prostaglandin E(2) (PGE(2)) in lipopolysaccharide (LPS) treated RAW264.7 cells. Sequentially, an animal model examination was performed to confirm the effects of HPE on LPS-induced hepatic inflammation. The results showed that HPE reduced 94.6% of xanthine oxidase activity in vitro, and decreased nitrite and PGE(2) secretions in LPS-induced cells. In LPS-treated rats, HPE significantly decreased the serum levels of alanine and aspartate aminotransferase. In the liver, lipid peroxidation and liver lesions decreased, and catalase activity and glutathione increased. The study also revealed that down-regulation of cyclooxygenase-2 (COX-2), p-c-Jun N-terminal kinase (p-JNK) and p-P38 might have been involved. In sum, this study found an anti-inflammatory potency of HPE both in vitro and in vivo.


Subject(s)
Antioxidants/metabolism , Cyclooxygenase 2/metabolism , Flavonoids/pharmacology , Gene Expression Regulation, Enzymologic/drug effects , Hibiscus/chemistry , Inflammation/metabolism , Lipopolysaccharides/antagonists & inhibitors , Phenols/pharmacology , Animals , Anti-Inflammatory Agents/isolation & purification , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/therapeutic use , Cell Line , Flavonoids/isolation & purification , Flavonoids/therapeutic use , Inflammation/chemically induced , Inflammation/drug therapy , Inflammation/pathology , Lipid Peroxidation/drug effects , Lipopolysaccharides/toxicity , Liver/cytology , Liver/drug effects , Liver/pathology , Macrophages/drug effects , Macrophages/metabolism , Male , Mitogen-Activated Protein Kinase Kinases/metabolism , Nitric Oxide Synthase Type II/metabolism , Phenols/isolation & purification , Phenols/therapeutic use , Plant Extracts/chemistry , Polyphenols , Rats , Xanthine Oxidase/metabolism
4.
Nutrition ; 21(7-8): 779-85, 2005.
Article in English | MEDLINE | ID: mdl-15975484

ABSTRACT

OBJECTIVES: This study assessed the effect of vitamin B6 status on immune responses in mechanically ventilated, critically ill patients and compared the results with those of healthy controls. METHODS: This was designed as a cross-sectional observational study. Forty patients in the intensive care unit successfully completed this study. Vitamin B6 intake was recorded for 8 d. Severity of illness (Second Acute Physiology and Chronic Health Evaluation score) was recorded. Thirty-eighty healthy controls were recruited from the physical check unit of Taichung Veterans General Hospital (Taichung, Taiwan). All control subjects were given instruction on how to complete a 24-d diet recall. Vitamin B6 status was assessed by direct measures (plasma pyridoxal 5'-phosphate [PLP] and 4-pyridoxic acid) and indirect measures (erythrocyte alanine and aspartate aminotransferase activity coefficients). Levels of serum albumin, hemoglobin, hematocrit, high-sensitivity C-reactive protein, and immune responses (white blood cell, neutrophil, total lymphocytes, T lymphocytes [CD3], B lymphocytes [CD19], T-helper cells [CD4], and suppressor cells [CD8]) were determined. RESULTS: Critically ill patients had sufficient vitamin B6 intake but showed marginal PLP deficiency (20.9 +/- 1.5 nmol/L). In addition, critically ill patients had significantly lower and abnormal immune responses than did healthy controls. There was no significant correlation of vitamin B6 intake and erythrocyte alanine and aspartate aminotransaminase activity coefficients with immune indices. Plasma PLP concentration was strongly negatively correlated with high-sensitivity C-reactive protein level. However, plasma PLP was significantly associated with immune responses after adjustment for age, sex, high-sensitivity C-reactive protein, and the other four vitamin B6 indicators. CONCLUSIONS: Plasma PLP is a significant indicator of immune responses in human subjects. Further research is warranted to study whether vitamin B6 supplementation in critically ill patients improves their immune responses.


Subject(s)
Critical Illness , Pyridoxal Phosphate/blood , Pyridoxal Phosphate/deficiency , Respiration, Artificial , Vitamin B 6 Deficiency/immunology , Vitamin B 6/administration & dosage , APACHE , Adult , Aged , Aged, 80 and over , Alanine Transaminase/metabolism , Aspartate Aminotransferases/metabolism , C-Reactive Protein , Case-Control Studies , Critical Illness/therapy , Cross-Sectional Studies , Erythrocytes/enzymology , Female , Health Status Indicators , Hospitalization , Humans , Lymphocytes/blood , Male , Mental Recall , Middle Aged , Nutritional Status , Pyridoxal Phosphate/immunology , Severity of Illness Index , Vitamin B 6/analogs & derivatives , Vitamin B 6 Deficiency/blood
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