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1.
Chinese journal of integrative medicine ; (12): 287-292, 2005.
Article in English | WPRIM | ID: wpr-314101

ABSTRACT

<p><b>OBJECTIVE</b>To explore the effects of total flavonoids of Hippophae rhamnoides L. (TFH), quercetin (Que) and isorhamnetin (Isor) on the intracellular free calcium ([Ca(2+)](i)) in vascular smooth muscle cells (VSMC) of spontaneously hypertensive rats (SHR) and Wistar-Kyoto rats (WKY).</p><p><b>METHODS</b>Fluo 3-acetoxymethylester (Fluo-3/AM) was used to observe the effects of TFH (100 mg/L) and its essential monomers, namely Que (10(-4) mol/L) and Isor (10(-4) mol/L) on changes of [Ca(2+)](i) in cultured SHR and WKY VSMC (abbr. to Ca-SHR & Ca-WKY) following exposure to high K(+), norepinephrine (NE) and angiotensin II (Ang II), and to compare with the effects of verapamil (Ver).</p><p><b>RESULTS</b>(1) TFH, Que and Isor had inhibitory effects on resting Ca-SHR (P < 0.05), but had no significant effects on Ca-WKY (P > 0.05). (2) High K(+) could increase Ca-SHR more significantly than Ca-WKY (P < 0.05); TFH, Que and Isor could inhibit the elevation of [Ca(2+)](i) induced by high K(+)-depolarization, with the effects similar to that of Ver, and the effect on Ca-SHR was more significant than that on Ca-WKY (P < 0.05). (3) NE and Ang II could increase Ca-SHR more significantly than Ca-WKY (P < 0.05), TFH, Que and Isor had remarkably inhibitory effect on the elevation of Ca-SHR and Ca-WKY induced by NE or Ang II. (4) In the absence of extracellular Ca(2+), TFH, Que and Isor also had certain inhibitory effect on Ca-SHR and Ca-WKY induced by NE, and the effect on the former was more significant than that on the latter (P < 0.05).</p><p><b>CONCLUSION</b>TFH, Que and Isor might decrease the levels of [Ca(2+)](i) in VSMCs by blocking both voltage-dependent calcium channels (VDC) and receptor-operated calcium channels (ROC) in physiological or pathological state, which may be one of the important mechanisms of their hypotensive and protective effects on target organs in patients with hypertension.</p>


Subject(s)
Animals , Rats , Angiotensin II , Pharmacology , Calcium , Cells, Cultured , Flavonoids , Pharmacology , Flavonols , Pharmacology , Hippophae , Hypertension , Metabolism , Muscle, Smooth, Vascular , Chemistry , Cell Biology , Norepinephrine , Pharmacology , Quercetin , Pharmacology , Rats, Inbred SHR , Rats, Inbred WKY , Verapamil , Pharmacology
2.
Southeast Asian J Trop Med Public Health ; 2002 Sep; 33(3): 551-6
Article in English | IMSEAR | ID: sea-33175

ABSTRACT

The genotype of Orientia tsutsugamushi DNA from mites in the Xisa archipelago of China were identified. A natural focus of tsutsugamushi disease in the archipelago was found. The DNA sequence that codes for the 56 kDa protein of O. tsutsugamushi was amplified by nested polymerase chain reaction (N-PCR). The purified positive products were cloned into a pGEM-T vector and sequenced. The DNA sequence was compared with various sequences on the internet for sequence homology. A 507 bp DNA fragment encoding the 56 kDa protein was amplified from the samples. The sequence homology was 85% (Karp strain), 68% (Gilliam strain), 65% (Kato strain), and 67% (Yonchon strain). Orientia tsutsugamushi is carried by the mites of the Xisa archipelago; the main genotype is the Karp strain.


Subject(s)
Animals , Bacterial Typing Techniques/methods , China , DNA, Bacterial/analysis , Genotype , Humans , Mites/microbiology , Orientia tsutsugamushi/classification , Polymorphism, Restriction Fragment Length , Reference Values
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