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bromelin/uždegimas

Nuoroda įrašoma į mainų sritį
StraipsniaiKlinikiniai tyrimaiPatentai
9 rezultatus

[Clinical experience with methoxybutropate vs. bromelin in the treatment of female pelvic inflammation].

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This study reports the results of a controlled randomized clinical trial performed on 30 young women with PID (Pelvic Inflammatory Disease), using a new anti- inflammatory-analgesic: methoxybutropate. The quali-quantitative symptomatical assessment showed that the improvement of the pain has been

[Combination of deoxyribonuclease and bromelin in the therapy of gynecologic pelvic inflammations].

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[TREATMENT OF INFLAMMATION AND EDEMA WITH BROMELIN. A CONCENTRATED PLANT PROTEOLYTIC ENZYME].

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[Probable coumarin poisoning upon ingestion of an anti-inflammatory agent].

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Warfarin overdose leads to hypoprothrombinemia and bleeding diathesis. We report here the case of a 47 year old woman who ingested an overdose of a non-steroidal anti-inflammatory drug, sold in Mexico under the name of Wobenzym (R), and containing, according to the manufacturer: pancreatin,

Asthma caused by bromelin inhalation.

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Two cases are reported of bronchial asthma caused by inhalation of bromelin, a proteolytic enzyme utilized in some anti-inflammatory medicine. Prick test results with bromelin extract were positive. Inhalation tests gave immediate reactions which were blocked by sodium cromoglycate, but not
BACKGROUND Matrix metalloproteinase-9 (MMP9) expression due to ischemic cause spreading of brain damage. Previous studies have reported that Bromelin was beneficial as anti-inflammation and prevent brain tissue damage. OBJECTIVE This study aimed to determine the alteration of plasma MMP9 level after

Involvement of heparan sulfate in 67Ga binding to rat-liver plasma membrane.

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The role of heparan sulfate (HS) in gallium citrate Ga 67 binding to rat-liver plasma membrane was investigated. HS was found to be the only acid mucopolysaccharide present on the plasma-membrane surface. The extent of 67Ga binding to the plasma membrane reached a plateau 1-2 h after the start of

Myo-inositol modulates insulin and luteinizing hormone secretion in normal weight patients with polycystic ovary syndrome.

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OBJECTIVE To investigate hormonal dynamics in a group of non-obese polycystic ovary syndrome (PCOS) patients under myo-inositol (MYO) administration. METHODS Hormonal profiles, insulin response to oral glucose tolerance test (OGTT) and luteinizing hormone (LH) response to gonadotropin-releasing
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