Functional changes in vascular smooth muscle and endothelium of arteries during diabetes mellitus

Life Sciences

Volumn 50, Issue 19, 1992, Pages 1379-1387

  Kamata, Katsuo ^a   Miyata, Noriyuki ^b   Abiru, Toichi ^c   Kasuya, Yutaka ^a  

^a HOSHI UNIVERSITY   (Japan)

^b TAISHO PHARMACEUTICAL CO LTD   (Japan)

^c YAMASA CORPORATION   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1,4 DIHYDRO 2,6 DIMETHYL 5 NITRO 4 [2 (TRIFLUOROMETHYL)PHENYL] 3 PYRIDINECARBOXYLIC ACID METHYL ESTER; ACETYLCHOLINE; ALPHA ADRENERGIC RECEPTOR; BETA ADRENERGIC RECEPTOR; CALCIUM CHANNEL; CYCLIC GMP; ENDOTHELIUM DERIVED RELAXING FACTOR; INOSITOL PHOSPHATE; ISOPRENALINE; NORADRENALIN; POTASSIUM CHANNEL; VASOACTIVE AGENT;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CARDIOVASCULAR DISEASE; DIABETES MELLITUS; NONHUMAN; PHOSPHOINOSITIDE METABOLISM; PRIORITY JOURNAL; RABBIT; RAT; VASCULAR ENDOTHELIUM; VASCULAR SMOOTH MUSCLE;

ANIMAL; DIABETIC ANGIOPATHIES; ENDOTHELIUM, VASCULAR; ION CHANNELS; MUSCLE, SMOOTH, VASCULAR; PHOSPHATIDYLINOSITOLS; RECEPTORS, ADRENERGIC;

ANIMALIA; ORYCTOLAGUS CUNICULUS;

EID: 0026583353     PISSN: 00243205     EISSN: None     Source Type: Journal    
DOI: 10.1016/0024-3205(92)90256-O     Document Type: Article

References (77)

1. Oxygen free radicals abolish endothelium-dependent relaxation in diabetic rat aorta.
2. Impairment of endothelium-dependent dilatation of cerebral arterioles during diabetes mellitus.
3. Contraction of diabetic rabbit aorta caused by endothelium-derived PGH2-TxA2.