1.Expression of P-selectin in the penile vascular epithelia of smoking rats.
Hua YANG ; Dong-Wen WANG ; Wei-Bing SHUANG ; Jing-Qi WANG ; Li ZHANG ; Bin ZHAO ; Jian ZHANG
National Journal of Andrology 2008;14(12):1094-1098
<p>OBJECTIVETo observe the expression of P-selectin in the penile vascular epithelial cells and the morphological changes in the ultrastructure of the penile cavernous tissues of smoking rats, and to explore the pathogenesis of smoking-induced erectile dysfunction.p><p>METHODSFifty healthy Wistar rats were randomly divided into a normal control, a long-term heavy smoking group, a long-term light smoking, a short-term heavy smoking and a smoking cessation group. Their erectile function was tested by subcutaneous injection of apomorphine (APO), the P-selectin expression in the penile vascular epithelial cells detected by ELISA and the morphological changes in the ultrastructure of the penile cavernous tissues observed under the transmission electron microscope (TEM).p><p>RESULTSThe levels of P-selectin were 10.78 +/- 1.71 ng/L, 62.62 +/- 5.95 ng/L, 40.06 +/- 3.97 ng/L, 41.37 +/- 4.06 ng/L and 22.80 +/- 3.15 ng/L respectively in the normal control, long-term heavy smoking, long-term light smoking, short-term heavy smoking and smoking cessation groups, with significant differences between the control group and the other four (P < 0.05). Electron microscopy showed abnormal arrangement of endothelia, penile cavernous sinuses and smooth muscle cells, disrupted continuity of endothelia, damaged ultrastructure of endothelial and smooth muscle cells in the penile cavernous tissue, and obvious proliferation and fibrosis of interstitial tissues in the smoking rats.p><p>CONCLUSIONSmoking increases the P-selectin expression in the penile vascular epithelial cells and damages the ultrastructure of the penile cavernous tissue, which may be the main contributors to smoking-induced erectile dysfunction.p>
Animals
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Epithelium
;
metabolism
;
Male
;
P-Selectin
;
biosynthesis
;
Penile Erection
;
Penis
;
blood supply
;
metabolism
;
ultrastructure
;
Rats
;
Rats, Wistar
;
Smoking
;
adverse effects
2.Experimental study on cryopreservation of platelets.
Hui-Yun YANG ; Wei TIAN ; Ying GUO ; Rui-Li ZHANG ; Wang-Gang ZHANG
Journal of Experimental Hematology 2007;15(2):408-411
The study was purposed to develop a novel cryopreserved agent (CPA) for platelets, to investigate the morphology of cryopreserved platelets in different CPA and the CD62P expression on membrane of platelets after stimulating by thrombin, as well as to compare the effect of adding UDP-Gal on preserved efficiency of preservation solutions. A novel cryopreserved agent consisting of 2% DMSO, thrombosol and UDP-Gal was developed on basis of using higher concentration of DMSO. The morphology of chilled platelets was observed by transmission electron microscope and compared with fresh platelets. The expression of CD62P on the membrane of platelets was detected at 0, l, 3 months. The results indicated that the significant effect of cryopreservation on morphology of platelets was found according to percentages of round, dendritic and irregular shapes of cryopreserved platelets. The protective effects of 2% DMSO + thrombosol and 2% DMSO + thrombosol + UDP-Gal were better than that of 5% DMSO. Compared with fresh platelets, the expression of CD62P on platelet membrane decreased obviously after cryopreservation, but not observed difference at preservation for 1 month and 3 months, as well as among 3 kinds of different CPA. It is concluded that the protective effects of 2% DMSO + thrombosol and 2% DMSO + thrombosol + UDP-Gal on morphology of platelets are similar, but better than that 5% DMSO. The reaction of cryopreserved platelets to thrombin decreases, while the significant difference is not found among these 3 kinds of CPA. The addition of UDP-Gal to cryopreserved agents not show the protective effect on platelets.
Blood Platelets
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Blood Preservation
;
methods
;
Cryopreservation
;
methods
;
Cryoprotective Agents
;
pharmacology
;
Dimethyl Sulfoxide
;
pharmacology
;
Humans
;
P-Selectin
;
biosynthesis
;
genetics
;
Uridine Diphosphate Galactose
;
pharmacology
3.Platelet and tissue factor: review.
Journal of Experimental Hematology 2006;14(5):1065-1068
It is generally accepted that tissue factor plays an important role in coagulation and intravascular thrombus formation. Tissue factor is not only found primarily on the surface of certain cells that are located outside the vasculature, but also found in circulating cells. Monocyte express tissue factor induced by endotoxin. Recently, many researches indicate that P-selectin, CD40 ligand and GPIIb/IIIa receptor of platelet can also affect expression of tissue factor by monocyters. In addition, a lot of studies showed that tissue factor exist in the circulation including contained platelet. Tissue factor in the platelet releases under certain condition, and initiates coagulation. In this review the relation between platelet and tissue factor was elaborated.
Blood Platelets
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drug effects
;
metabolism
;
physiology
;
CD40 Ligand
;
physiology
;
Humans
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Monocytes
;
drug effects
;
metabolism
;
P-Selectin
;
physiology
;
Peptides
;
pharmacology
;
Platelet Glycoprotein GPIIb-IIIa Complex
;
physiology
;
Thromboplastin
;
biosynthesis
;
drug effects
;
physiology
4.Effect of erigeron injection on platelet level of CD62p and serum content of TNF-alpha and IL-6 in patients with acute cerebral infarction.
Jin-Liang WANG ; Wei GU ; Feng TAN
Chinese Journal of Integrated Traditional and Western Medicine 2005;25(4):324-326
<p>OBJECTIVETo investigate the clinical effect of Erigeron injection (El) on positive expression rate of CD62p in platelet and content of tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) in serum of patients with acute cerebral infarction (ACI).p><p>METHODSSixty-eight patients with ACI were randomly divided into the treated group (n = 35) and the control group (n = 33). Conventional treatment were given to both groups, and EI 40 ml/d were given additionally to the treated group, the treatment course for both groups was 15 days. The positive expression of platelet CD62p and the serum TNF-alpha and IL-6 in patients before and after treatment were determined with flow cytometric (FCM) and electrochemical-luminescence (ECL) techniques respectively.p><p>RESULTSThe total curative effect in the treated group were significantly higher than that in the control group (P < 0.05). Levels of platelet CD62p and serum TNF-alpha and IL-6 in ACI patients before and after treatment were significant higher than those in the healthy group (P < 0.05), all the three parameters were significantly decreased after treatment, and the lowering in the treated group was more significant than that in the control group (P < 0.05).p><p>CONCLUSIONThe effect of El on ACI patients may relate to its action in down-regulating the expression of platelet CD62p, alleviating the immune response and inflammatory injury of central nervous system induced by cytokines.p>
Aged
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Aged, 80 and over
;
Asteraceae
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chemistry
;
Blood Platelets
;
metabolism
;
Cerebral Infarction
;
immunology
;
metabolism
;
Drugs, Chinese Herbal
;
therapeutic use
;
Female
;
Humans
;
Injections
;
Interleukin-6
;
blood
;
Male
;
Middle Aged
;
P-Selectin
;
biosynthesis
;
blood
;
Phytotherapy
;
Tumor Necrosis Factor-alpha
;
metabolism
5.Study on platelet activated state and platelet activated function in adults with acute leukemia.
Wen-Da LUO ; Bao-Guo CHEN ; Zhe-Feng MEN ; Bo-Li LI ; Min ZHU ; Qun-Yi GUO
Journal of Experimental Hematology 2005;13(3):452-455
To investigate the changes of platelet activated state and platelet activated function by trace whole blood flow cytometry (FCM), and to explore the mechanism of hemorrhage and infiltration in adults with acute leukemia, the expression percentage and changes of these expressions of CD62p and PAC-1 on platelet surface were determined by FCM of trace whole blood after platelet activated by ADP in patients with new diagnosed AL (group I), complete remission (CR, group II) and continuously complete remission (CCR, group III). Healthy adults were used as control group. The result showed that the expression of CD62p in group I and II was higher than that in control group, before and after platelet activated by ADP (P < 0.01). The expression of PAC-1 in group I was higher than that in control group (P < 0.01), the expression of PAC-1 in group II was lower than that in control group (P > 0.01), There was no significant difference in expression of CD62p and PAC-1 between group III and control group (P > 0.01), and no significant difference was found between AL group with megakaryocyte malignant pathological changes and AL group without megakaryocyte malignant pathological changes before platelet activated by ADP (P > 0.01). After platelet activated by ADP, the expression of PAC-1 in the former was lower than that in the latter (P < 0.01). It is concluded that (1) high level activated platelet in peripheral blood of AL patients show that interaction between activated platelet and leukemia cells can be one of reason resulting in widespread hemorrhage and infiltration AL patiens; (2) the decrease of number and activted function of platelet at the first stage of AL patients may be caused by malignant hyperplasia of leukemia cells and damage of megakaryopoiesis in bone marrow.
Acute Disease
;
Adenosine Diphosphate
;
pharmacology
;
Adolescent
;
Adult
;
Aged
;
Blood Platelets
;
cytology
;
metabolism
;
Cell Membrane
;
drug effects
;
metabolism
;
Female
;
Flow Cytometry
;
Humans
;
Leukemia
;
blood
;
pathology
;
Male
;
Middle Aged
;
P-Selectin
;
biosynthesis
;
Platelet Activation
;
drug effects
;
physiology
;
Platelet Glycoprotein GPIIb-IIIa Complex
;
biosynthesis
6.The study of yi-shen-huo-xue fang's effects on expression of GMP-140 and cleaning out the oxygenic free radicle on rabbits blood stasis model.
Xiao-ping ZHAN ; Qing FANG ; Jian-guo LOU ; Xi-hong XU ; Xiao-ying JIN ; Guang-ming QIN ; Jun BAO
China Journal of Chinese Materia Medica 2003;28(4):355-358
<p>OBJECTIVETo evaluate the effects of Yi-Shen-Huo-Xue Fang on expression of GMP-140 and cleaning out the oxygenic free radicle on rabbits blood stasis model.p><p>METHODThirty rabbits were divided randomly into five groups as the normal group, model group, large dose of "Yi-Shen-Huo-Xue Fang" group, small dose of "Yi-Shen-Huo-Xue Fang" group and "Xue-Shuan-Xin-Mai-Ning" group. After being treated respectively, granule membrane protein 140(GMP-140), erythrocyte sueroxide dismutase (E-SOD), erythrocyte lipid peroxide(E-LPO), plasma lipid peroxide(P-LPO) were checked up.p><p>RESULTThe GMP-140, E-SOD, E-LPO, P-LPO in normal control were compared with those in model groups, With the difference(P < 0.01), model control group was compared with large dose group and small dose group (P < 0.01), with "Xue-Shuan-Xin-Mai-Ning" group(P < 0.05), large dose group was compared with "Xue-Shuan-Xin-Mai-Ning" group(P < 0.05), and large dose group were compared with small dose group (P > 0.05).p><p>CONCLUSIONThe model was made successfully. Large dose group, small dose group and "xue-shuan-xin-mai-ning" group can inhibit expression of GMP-140, enhence SOD activity and decrease LPO content on blood stasis rabbit model. Large dose group and small dose group have stronger effect than "xue-shuan-xin-mai-ning" group.p>
Animals
;
Drug Combinations
;
Drugs, Chinese Herbal
;
isolation & purification
;
pharmacology
;
Erythrocytes
;
metabolism
;
Female
;
Free Radical Scavengers
;
pharmacology
;
Lipid Peroxides
;
blood
;
Male
;
Medicine, Chinese Traditional
;
P-Selectin
;
biosynthesis
;
Plants, Medicinal
;
chemistry
;
Rabbits
;
Random Allocation
;
Superoxide Dismutase
;
blood
7.Determination of tolerance ability of platelet to the change of solution osmotic pressure and its significance.
Xi-Lin OUYANG ; Jing-Han LIU ; Dayong GAO
Journal of Experimental Hematology 2003;11(1):89-91
In order to determine the tolerance ability of platelet to change of osmotic pressure in solution, the isotonic fresh platelets were exposed to a series of crystal salt solutions with osmotic pressure range from 47 to 611 mOsm for 15 minutes. Then the platelets were returned to isotonic condition and kept for 15 minutes. The expressions of phosphatidylserine and CD62p were assayed in platelets. The results showed that the phosphatidylserine and CD62p expressions were increased when the osmotic pressure of solution was below 238 mOsm, but no significant rise was detected when the platelets were exposed to 611 mOsm solution. No increases of positive rate of CD62p and phosphatidylserine were detected in platelets returned to isotonic condition. It is concluded that platelets are sensitive to hypoosmotic solution and tolerated to hyperosmotic solution. Exceeding the platelet safe volume limitation may lead to injure of platelet osmosis in crystal salt solution.
Blood Platelets
;
drug effects
;
metabolism
;
Humans
;
Hypotonic Solutions
;
pharmacology
;
Isotonic Solutions
;
pharmacology
;
Osmotic Pressure
;
P-Selectin
;
biosynthesis
;
Phosphatidylserines
;
biosynthesis
;
Saline Solution, Hypertonic
;
pharmacology
;
Sodium Chloride
;
pharmacology
8.Surface Expression of P-selectin on Platelets Is Related with Clinical Worsening in Acute Ischemic Stroke.
Jae Kwan CHA ; Min Ho JEONG ; Eun Kyung KIM ; Yeong Jin LIM ; Byung Ryp HA ; Sang Ho KIM ; Jae Woo KIM
Journal of Korean Medical Science 2002;17(6):811-816
Platelet activation has a critical role in arterial disorders. In this study, we showed that the upregulation of P-selectin expression on platelets was related with clinical worsening in acute ischemic stroke. We serially (within 24 hr, at 72 hr, and 7 days) measured the expression of P-selectin on platelets in patients with acute ischemic stroke (n=45) and investigated the correlation between their extents and clinical severity of ischemic stroke. A significant relationship between the P-selectin expressions and National Institute of Health Stroke Scale (NIHSS) was observed at 72 hr and 7 days after ischemic stroke onset. Patients with clinical deterioration showed significantly increased expression of P-selectin on platelets as compared to those without deterioration. These results suggest that the P-selectin expression on platelets may contribute to the aggravation of clinical course in acute ischemic stroke. Thus, adequate manipulation of activated platelets is an important therapeutic strategy in acute ischemic stroke.
Adult
;
Aged
;
Aged, 80 and over
;
Arteriosclerosis/pathology
;
Blood Platelets/*metabolism
;
Brain Ischemia/*metabolism
;
Cell Adhesion Molecules/metabolism
;
Cerebrovascular Disorders/metabolism
;
Disease Progression
;
Female
;
Flow Cytometry
;
Humans
;
Male
;
Middle Aged
;
P-Selectin/*biosynthesis/blood
;
Signal Transduction
;
Stroke/metabolism
;
Time Factors
;
Up-Regulation
9.Flow cytometry combined assay for phosphatidylserine and CD62p expressed by preserved platelets.
Xi-Lin OUYANG ; Jing-Han LIU ; Qun LUO ; Qun SHI ; Wei HAN ; Xi-Jin LI ; Dayong GAO
Journal of Experimental Hematology 2002;10(1):66-69
Human platelets have distinct characters when preserved by different methods. A efficient flow cytometric assay for different preserved platelets expression of CD62p and phosphatidylserine(PS) is in dire need. Efficient flow cytometric assay for CD62p and PS expressed by preserved platelets was established and the major conditions were optimized. The platelets need not to be washed to wipe off plasma and can be labelled diredtly during the sample preparation. It is efficient for flow cytometric analysis when fresh platelet riched plasma (FPRP) was set as negative control, thrombin actived FPRP, and liquid nitrogen treated FPRP were set as positive control respectively. Gly-Pro-Arg-Pro acetate salt (GPRP) was applied to prevent platelets aggregation and fibrin formation, stabilize platelets and minimize the artificial platelets activation. This is also the key to conquer difficulty of flow cytometric quantitive analysis when platelet, Ca(2+) and plasma coexist. This flow cytometric method is specially suitable for the multi-parameter assay including PS expression for cryopreserved platelets. Minimal sample manipulation, no fixation, and GPRP application resulted in minor artifacts and good sample stability. Results suggested, this flow cytometric assay for preserved platelets is simple and efficient. In addition, the author prepared four different methods treated platelets that can be easily distinguished through this flow cytometric assay. It not only makes sure the practicability of this flow cytometric assay, but also suggests the value of the treated platelets applied in preserved platelets flow cytometric ass
Blood Platelets
;
metabolism
;
Flow Cytometry
;
methods
;
Humans
;
P-Selectin
;
biosynthesis
;
Phosphatidylserines
;
analysis
;
Reproducibility of Results
;
Tissue Preservation
10.CD62p expression in platelet during the preparation course of Cryopreservated platelet-rich plasma.
Jing-Han LIU ; Xi-Lin OUYANG ; Qun SHI ; Qun LUO ; Xi-Jin LI ; Hai-Bao WANG ; Min-Cai CHENG ; Wei HAN ; Dayong GAO
Journal of Experimental Hematology 2002;10(3):253-256
In order to explore the factors that affect CD62p expression in platelet during the whole course of cryopreservated platelets preparation, CD62p expression of platelet was evaluated by flow cytometry assay. The whole course of cryopreservated platelets preparation in order included whole blood collection, centrifugation for fresh platelet-rich plasma preparation, addition of dimethyl sulfoxide, and freeze in -80 degrees C refrigerator and thaw in 38 degrees C water bath. Result showed that the CD62p expressed slowly from whole blood collection to addition of dimethyl sulfoxide, but expressed abruptly after freeze and thaw and it occupied 82 per cent of the whole expression. It was concluded that the whole blood collection, centrifugation for fresh platelet enriched plasma preparation and addition of dimethyl sulfoxide were optimized in the whole course, but the damage to platelets in the whole course of cryopreservation could not be avoided. It suggests that improved techniques are needed to reduce the damage to cryopreservated platelets.
Blood Platelets
;
metabolism
;
Blood Preservation
;
methods
;
standards
;
Cryopreservation
;
methods
;
standards
;
Flow Cytometry
;
Humans
;
P-Selectin
;
biosynthesis

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