Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
Add filters








Language
Year range
1.
Chinese Journal of Rehabilitation Theory and Practice ; (12): 1043-1046, 2019.
Article in Chinese | WPRIM | ID: wpr-905118

ABSTRACT

Secondary limb lymphedema is one of the common postoperative complications of breast cancer and gynecological malignant tumor. Tissue fibrosis is an important pathological change after lymphedema. It is also an important index to judge the severity and therapeutic effect of lymphedema. Tissue fibrosis can be evaluated indirectly from lymphedema or directly with instruments, and treated with comprehensive exercises, Heating and Bandage, and shock wave, etc.

2.
Chinese Journal of Applied Physiology ; (6): 184-188, 2014.
Article in Chinese | WPRIM | ID: wpr-236351

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the antithrombotic effects and its molecular mechanisms of prazosin combined with anisodamine (Ani).</p><p><b>METHODS</b>Isolated rat tail artery rings model was employed to evaluate the vasodilative effects of drugs, mice tail thrombosis model induced by carrageenan was used to study the antithrombotic effects and its molecular mechanisms of the drug composition.</p><p><b>RESULTS</b>Among alpha1-adrenoreceptor antagonists, prazosin(Pra) had the greatest relaxation rate, which was (82.6 +/- 8.9)%, and the EC50 value was 0.44 micromol/L. The drug composition of anisodamine and prazosin of different doses could decrease the length of the tail thrombosis from (24.6 +/- 4.6)mm to (6.9 +/- 2.7)mm, and the rate of thrombosis was decreased from 86.6% to 50.0%. The drug composition could prolong the prothrombin time (PT) distinctively, but it had no effect on the activated partial thromboplastin time (APTT). It also could restrain the decrease of serum levels of tissue plasminogen activator (t-PA) and 6- Keto -PGF1alpha as well as the increase of type-1 plasminogen activator inhibitor (PAI-1) and thromboxane B2 (TXB2) in the mice.</p><p><b>CONCLUSION</b>The drug composition formed by anisodamine and prazosin has good effects of relaxing extremities tiny blood vessels and it can fight against thrombosis, its antithrombotic mechanisms may be related to the influence of the extrinsic coagulation pathway, inhibition of platelet activation functions and the promotion of fibrinolysis function.</p>


Subject(s)
Animals , Male , Rats , Adrenergic alpha-1 Receptor Antagonists , Pharmacology , Disease Models, Animal , In Vitro Techniques , Prazosin , Pharmacology , Rats, Wistar , Solanaceous Alkaloids , Pharmacology , Thrombosis , Drug Therapy
3.
Chinese Journal of Applied Physiology ; (6): 204-207, 2014.
Article in Chinese | WPRIM | ID: wpr-236346

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the changes of vasoconstriction and vasodilatation under different temperature conditions and the protective effects of Vitamin E (Vit E) against endothelial injury induced by hypothermia.</p><p><b>METHODS</b>The tail arterial rings were prepared for isometric tension recording using multi wire myograph system. The effect of temperature on relaxation and construction was evaluated. Incubate the arterial rings with different concentration of Vit E when they were exposed to hypothermia, then acetylcholine (ACh)-induced endothelium-dependent relaxation was investigated to evaluate the activity of endothelial.</p><p><b>RESULTS</b>(1) The hypothermia could enhanced the dose-dependent construction induced by PE in mice tail artery. (2) Exposure to hypothermia also resulted in increase of sodium nitroprusside (SNP)-induced re-After incubation with Vit E, the vascular relaxation responses to ACh increased in an endothelium-dependent manner, when compared with the hypothermia-treated group.</p><p><b>CONCLUSION</b>The vascular function of constriction was attenuated by hypothermia, while the relaxation was increased. Vit E could prevent the hypothermia-induced decrease in vascular endothelial cells.</p>


Subject(s)
Animals , Male , Mice , Arteries , Physiology , Cold Temperature , Hypothermia , In Vitro Techniques , Prazosin , Pharmacology , Solanaceous Alkaloids , Pharmacology , Vasoconstriction , Vasodilation , Vasodilator Agents , Pharmacology , Vitamin E , Pharmacology
4.
Chinese Journal of Applied Physiology ; (6): 1-3, 2014.
Article in Chinese | WPRIM | ID: wpr-235311

ABSTRACT

<p><b>OBJECTIVE</b>To study the selective dilatation effects of iptakalim (Ipt) on basilar and pulmonary arterioles, and endothelial cell function of these arterioles in hypoxic rats.</p><p><b>METHODS</b>SD male rats were divided into 2 groups:control and hypoxic group fed in normobaric hypoxic environment (O2 7.8%, 8 h). Arteriole rings about (204 + 5) pm were isolated and the tension of hypoxic arterioles pre-contracted by 6 nmol/L endothelin-1 (ET-1) was observed with wire myograph system model (DMT 610 m). The relaxing response of hypoxic arterioles induced by different concentration of Ipt were detected and endothelial activity was also tested by acetylcholine.</p><p><b>RESULTS</b>10(5) mol/L acetylcholine (ACh)-mediated vasodilatation of basilar and pulmonary arterioles was greatly reduced in the hypoxic group than those in control group (P < 0.05). Compared with normal group, a novel ATP-sensitive potassium channel opener Ipt at the concentration ranging from 10(-11) mol/L to 10(3) mol/L, caused stronger dose dependent vasodilatation on hypoxic pulmonary arterioles, and there was no significant difference between control and hypoxic basilar arterioles.</p><p><b>CONCLUSION</b>The endothelial function of basilar and pulmonary arterioles was damaged under hypoxic state, and Ipt selectively increased dilatation effects on hypoxic pulmonary arterioles, but not on hypoxic basilar arterioles which could improve high altitude pulmonary edema pathological state and be the novel drug in the treatment of pulmonary hypertension.</p>


Subject(s)
Animals , Male , Rats , Acetylcholine , Pharmacology , Altitude , Altitude Sickness , Arterioles , Dilatation , Endothelin-1 , Pharmacology , Hypoxia , KATP Channels , Propylamines , Pharmacology , Vasodilation , Vasodilator Agents , Pharmacology
5.
Chinese Journal of Applied Physiology ; (6): 333-336, 2013.
Article in Chinese | WPRIM | ID: wpr-235365

ABSTRACT

<p><b>OBJECTIVE</b>To study the selective dilatation effects of iptakalim (Ipt), a novel ATP-sensitive potassium channel opener, on pulmonary arterioles in hypoxic pulmonary hypertensive rat.</p><p><b>METHODS</b>SD male rats were divided into 3 groups, control group, the rest were fed in hypoxic and normobaric environment (O2 10% +/- 0.5%, 8 h/d and 6 d/week) and divided into hypoxia group and hypoxia plus acetazolamide (Acz) group (hypoxic rats were treated with ig acetazolamide (Acz) 80 mg x kg(-1) d(-1)) . After 12 weeks, pulmonary arteriole rings about (197 +/- 4) microm were isolated and the tension of hypoxic pulmonary arterioles pre-contracted by 6 nmol/L endothelin-1 (FT-1) was observed with wire myograph system model (DMT 610 m). The relaxing response of hypoxic pulmonary arterioles induced by different concentration of Ipt were detected and endothelial activity was also tested by acetylcholine.</p><p><b>RESULTS</b>10(-5) mol/L acetylcholine (ACh)-mediated vasodilatation was greatly reduced in the hypoxic group than those in control group (P < 0.01) and there was no significant difference between Acz treatment group and control group (P > 0.05). Ipt at the concentration ranging from 10(-11) mol/L to 10(-4) mol/L, caused dose dependent vasodilation on both hypoxic pulmonary arterioles and Acz treatment group (P > 0.05), but not on normal group.</p><p><b>CONCLUSION</b>The endothelial function of pulmonary arterioles was damaged under hypoxic pulmonary hypertensive state, and Ipt showed selective dilatation effects on hypoxic pulmonary arterioles. Acz could improve the dysfunction of endothelial cells induced by hypoxic pulmonary hypertensive state, which didn't affect the selective dilatation effects of Ipt on hypoxic pulmonary arterioles.</p>


Subject(s)
Animals , Male , Rats , Acetazolamide , Arterioles , Hypertension, Pulmonary , Hypoxia , Propylamines , Pharmacology , Pulmonary Artery , Rats, Sprague-Dawley , Vasodilator Agents , Pharmacology
SELECTION OF CITATIONS
SEARCH DETAIL