1.Effect of Oxygen on the Antidotal Action of Thiosulfate in Cyanide Poisoning.
Korean Journal of Preventive Medicine 1982;15(1):161-166
Cyanide poisoning is expected to be antagonized by the administration of oxygen, when it is administered in combination with the conventional cyanide antidote, sodium,thiosulfate. However, the antidotal efficacy and its exact mechanism of oxygen in cyanide poisoning is still a controversial one. To test the effect of oxygen on the antidotal action of thiosulfate ,in cyanide poisoning, author designed this study on the dose-mortality patterns for potassium cyanide in mice. Potency ratios derived from LDso values were compared in groups of mice treated with sodium thiosulfate alone and sodium thiosulfate with oxygen. These results indicated that oxygen enhances the anti-dotal effect of sodium thiosulfate, effectively. This fact demonstrates that oxygen is of importance in the treatment of cyanide poisoning.
Animals
;
Mice
;
Oxygen*
;
Poisoning*
;
Potassium Cyanide
;
Sodium
2.Takyo's Scientific Approach.
Journal of the Korean Medical Association 2001;44(2):127-133
No abstract available.
3.The Reason For Breast Feeding Failure.
Journal of the Korean Pediatric Society 1983;26(6):527-533
No abstract available.
Breast Feeding*
;
Breast*
4.ABO Gene Frequency in ABO Hemolytic Disease of Newborn.
Journal of the Korean Pediatric Society 1988;31(9):1105-1113
No abstract available.
Erythroblastosis, Fetal*
;
Gene Frequency*
;
Infant, Newborn
5.Intrauterine Growth of Korean Infants from 25 Weeks to 44 Weeks Gestation.
Journal of the Korean Pediatric Society 1990;33(7):887-900
No abstract available.
Humans
;
Infant*
;
Pregnancy*
6.Early Growth Patterns of Premature Infants Fed Premature Special Milk.
Journal of the Korean Pediatric Society 1984;27(8):766-771
No abstract available.
Humans
;
Infant, Newborn
;
Infant, Premature*
;
Milk*
9.Predominant Th2 type immune response in bronchoalveolar lavage fluid of patients with Mycoplasma pneumoniae pneumonia.
Chang Keun KIM ; Churl Young CHUNG
Journal of Asthma, Allergy and Clinical Immunology 1999;19(5):647-655
OBJECTIVE: Mycoplasma pneumoniae infection is known as one of the frequent causes of exacerbation of bronchial asthma and it can also be a trigger for the initiation of asthma. However, little is known about the pathogenesis of respiratory M. pneumoniae infection. Furthermore, there is little data on human cytokine production and its involvement in the pathogenesis of M. pneumoniae infection. In order to investigate the immunopathogenesis of M. pneumoniae infection, we investigated the cytokine production in the bronchoalveolar lavage ( BAL ) fluid of patients with M. pneumoniae pneumonia and viral pneumonia, and compared the results with those of control subjects. SUBJECT AND METHOD: BAL was performed with fiberoptic bronchoscopy in patients with M. pneumoniae pneumonia( n=9 ), viral pneumonia( n=9 ), and control subjects( n=6 ) aged 3 years to 9 years. M. pneumoniae pneumonia was documented by polymerase chain reaction and serologic analysis. Four respiratory viruses ( adenovirus, influenza A, influenza B, parainfluenza ) were detected by culture method. Cell pellets and supernatants were separated by centrifugation and Interleukin( IL ) - 2, Interferon( IFN )-r, IL-4, and IL-5 levels were measured in concentrated BAL supernatants by ELISA. RESULTS: Analysis of cytokines revealed significantly increased production of IL-4 ( p< 0.0001 ) and IL-2 ( p< 0.0001 ), in patients with M. pneumoniae pneumonia and significantly increased production of IL-2 (p <0.0001) in patients with viral pneumonia compared with those of the control subjects. Ratio of IL-4/IFN-r was significantly increased in patients with M. pneumoniae pneumonia ( p< 0.005 ) but not in patients with viral pneumonia compared with that of the control subjects. CONCLUSION: IL-4 production and IL-4/IFN-r ratio were increased in the BAL fluid of patients with M. pneumoniae infection. These findings suggest that predominant Th2 immune response could play an important role in the pathogenesis of M. pneumoniae infection.
Adenoviridae
;
Asthma
;
Bronchoalveolar Lavage Fluid*
;
Bronchoalveolar Lavage*
;
Bronchoscopy
;
Centrifugation
;
Cytokines
;
Enzyme-Linked Immunosorbent Assay
;
Humans
;
Influenza, Human
;
Interleukin-2
;
Interleukin-4
;
Interleukin-5
;
Mycoplasma pneumoniae*
;
Mycoplasma*
;
Paramyxoviridae Infections
;
Pneumonia*
;
Pneumonia, Mycoplasma*
;
Pneumonia, Viral
;
Polymerase Chain Reaction
10.The effects of compound madecassol on the wound healing.
Young Cheun YOO ; Seog Keun YOO
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1998;25(8):1451-1458
This study was designed to assess the effects of compound madecassol(madecassic acid with neomycin sulfate and hydrocortisone acetate) on the wound healing. Madecassol is a titrated extract of centella asiatica and the clinical effects of madecassol are stated to the enhancement of wound healing and the prevention and relief of excessive scar formation. Compound madecassol is composed of madecassol and neomycin sulfate and hydrocortisone acetate. Neomycin sulfate has antibiotic effect and hydrocortisone acetate has antiinflammatory and antiallergic effects. So, compound madecassol has a synergistic effect of madecassol as well as neomycin sulfate and hydrocortisone acetate. Using 54 rats, we compared the effect of compound madecassol on wound healing at 3rd, 7th, 14th, and 21th postoperative days. This study examined the histologic findings and the gross findings which were wound size, epithelization and quality of granulation tissue. In this study, compound madecassol showed lower degree of inflammatory infiltration, shorter inflammatory phases and less wound contraction. The number of the myofibroblast in the group of compound madecassol were fewer than other groups. Granulation tissue of the compound madecassol was relatively healthier than others. There were no significant difference of re-epithelization between compound madecassol and other groups. In conclusion, compound madecassol can reduce excessive wound contraction and promotes wound healing process.
Animals
;
Centella
;
Cicatrix
;
Granulation Tissue
;
Hydrocortisone
;
Myofibroblasts
;
Neomycin
;
Rats
;
Wound Healing*
;
Wounds and Injuries*