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1.
Int Angiol ; 36(6): 569-573, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28895368

ABSTRACT

BACKGROUND: Analyze the association of lower limb edema with venous reflux in healthy primigravidae during pregnancy and in the postpartum. METHODS: Cohort with primigravidae evaluated in the three trimesters of pregnancy and postpartum. Edema was assessed by physical examination. Duplex evaluated venous reflux in both limbs. RESULTS: In the first trimester, no woman presented edema or venous reflux. In the second trimester, venous reflux was found in one patient (5%) and edema was found in four women (20%). Venous reflux and edema were not associated (P=1). In the third trimester, two other patients developed venous reflux (15%) and eleven women developed lower limb edema (55%). Venous reflux and edema were also not associated (P=0.21). In the postpartum period, neither venous reflux nor lower limb edema were found. CONCLUSIONS: In healthy primigravidae, lower limb edema was not associated with venous reflux. Both were present in the second and in the third trimesters of pregnancy and resolved spontaneously in the postpartum period. Both are products of the same physiological changes that occur in pregnancy.


Subject(s)
Edema/etiology , Lower Extremity/blood supply , Pregnancy Complications/diagnostic imaging , Venous Insufficiency/diagnostic imaging , Adult , Female , Humans , Parity , Postpartum Period , Pregnancy , Prenatal Care , Prospective Studies , Ultrasonography, Doppler, Duplex
2.
J Invest Surg ; 29(1): 13-9, 2016.
Article in English | MEDLINE | ID: mdl-26375056

ABSTRACT

BACKGROUND: Bradykinin (BK) is used in different tissues. Dose-dependent studies have demonstrated that low doses protect against ischemia/reperfusion (I/R) injury while higher doses lead to adverse effects. Although the beneficial effects of BK infusion were observed in myocardium, its role on the I/R impact in skeletal muscle (SM) has not been fully clarified. OBJECTIVE: This study was carried out to evaluate the effects of BK, administered in the hindlimbs of rats subjected to I/R. METHODS: The study design included three experimental groups: Group 1 control (saline), Group 2 (bradykinin), and Group 3 (HOE 140, a BK2 receptor blocker). In all three groups, rats were subjected to hindlimb ischemia for a total of 2 h followed by continuous 4 h of reperfusion with pharmacological interventions. The methods include analysis of enzymes (lactate dehydrogenase-LDH and creatinine phosphokinase-CPK), cell membrane marker of injury (malondialdeyde-MDA), recruitment of neutrophils (myeloperoxidase-MPO), and apoptosis index (immunohistochemistry TUNEL in situ peroxidase dead end). RESULTS: Except for the apoptotic index, all parameters studied were shown to be elevated in the reperfusion group intervened with BK. The blocking of BK2 receptors by HOE 140 did not affect the I/R injury. CONCLUSION: After 2 h of total ischemia, infusion of bradykinin during 4 h of reperfusion, worsened the I/R injury in the hindlimb skeletal muscle.


Subject(s)
Bradykinin B2 Receptor Antagonists/administration & dosage , Bradykinin/analogs & derivatives , Reperfusion Injury/prevention & control , Vasodilator Agents/administration & dosage , Animals , Apoptosis , Bradykinin/administration & dosage , Creatine Kinase/blood , Creatine Kinase/metabolism , Hindlimb/physiopathology , L-Lactate Dehydrogenase/metabolism , Male , Malondialdehyde/blood , Malondialdehyde/metabolism , Muscle, Skeletal/metabolism , Muscle, Skeletal/physiopathology , Peroxidase/blood , Peroxidase/metabolism , Rats , Rats, Wistar , Reperfusion Injury/blood , Reperfusion Injury/metabolism
3.
Ann Vasc Surg ; 28(4): 1005-15, 2014 May.
Article in English | MEDLINE | ID: mdl-24440188

ABSTRACT

BACKGROUND: The kallikrein-kinin system (KKS) has several direct and indirect effects on cells and cellular mediators involved in the inflammatory process. Studies about inflammation on percutaneous transluminal angioplasty with stent (PTA/stent) to treat peripheral arterial disease (PAD) in humans are scarce. The matrix metalloproteinases (MMPs) are calcium-dependent zinc-containing endopeptidases expressed in various cells and tissues such as fibroblasts, inflammatory cells, and, smooth muscle cells. Changes in the extracellular matrix (ECM) take place in the pathogenesis of many cardiovascular pathologies. MMPs and their inhibitors (tissue inhibitors of metalloproteinases [TIMPs]) are crucial in ECM remodeling in both physiologic and pathologic conditions. The aim of this study was to evaluate the role of the KKS and the MMP metabolism, which are important mediators that may contribute to tissue repair, in the process of arterial restenosis due to intimal hyperplasia in the femoropopliteal segment with the aim of developing new interventions. METHODS: Thirty-nine consecutive patients were selected (regardless of ethnic group, age, or sex) for revascularization, who underwent PTA/stent of the femoropopliteal segment. Twenty-five patients with the same clinical characteristics who were scheduled for diagnostic angiography but not subjected to PTA/nitinol stent were also selected. The concentrations in blood of total and kininogen fractions were evaluated using immunoenzymatic methods. Plasma kallikrein was evaluated by the colorimetric method. Tissue kallikrein was evaluated by the spectrophotometric method. The activity of kininase II was measured by fluorometric analysis. Quantification of MMPs was performed by zymography, which is an electrophoresis technique, and TIMPs were measured by enzyme-linked immunosorbent assay. RESULTS: Among the 31 patients who completed the survey, there were 10 cases of angiographically defined restenosis of >50%, and 21 cases without restenosis. There was an increase in the concentrations of the substrates (high-molecular-weight kininogens and lower molecular weight kininogens) and enzymes (plasma and tissue kallikrein) in patients with restenosis, indicating activation of this inflammatory pathway in these patients. The activity of kininase II was not significantly different between the groups of patients studied. There were no statistical differences between restenosis and no restenosis patients for both MMPs and TIMPs dosage, but there is an upward trend of MMPs in time 6 months in patients with restenosis. CONCLUSIONS: With the aim of identifying factors contributing to restenosis after endovascular intervention, this study showed evidence of high activation of the KKS in the pathologic inflammatory process of PTA/stent restenosis. In the other hand, it could not show participation of metalloproteinase metabolism in PTA/stent restenosis.


Subject(s)
Angioplasty, Balloon/instrumentation , Femoral Artery , Kallikreins/blood , Kinins/blood , Metalloproteases/blood , Peripheral Arterial Disease/enzymology , Peripheral Arterial Disease/therapy , Popliteal Artery , Stents , Tissue Inhibitor of Metalloproteinases/blood , Aged , Angioplasty, Balloon/adverse effects , Biomarkers/blood , Case-Control Studies , Constriction, Pathologic , Female , Femoral Artery/diagnostic imaging , Humans , Hyperplasia , Male , Middle Aged , Neointima , Peripheral Arterial Disease/blood , Peripheral Arterial Disease/diagnosis , Popliteal Artery/diagnostic imaging , Radiography , Recurrence , Time Factors
4.
Photomed Laser Surg ; 30(8): 418-24, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22730913

ABSTRACT

OBJECTIVE: This study aimed to investigate the effect of 830 and 670 nm diode laser on the viability of random skin flaps in rats. BACKGROUND DATA: Low-level laser therapy (LLLT) has been reported to be successful in stimulating the formation of new blood vessels and reducing the inflammatory process after injury. However, the efficiency of such treatment remains uncertain, and there is also some controversy regarding the efficacy of different wavelengths currently on the market. MATERIALS AND METHODS: Thirty Wistar rats were used and divided into three groups, with 10 rats in each. A random skin flap was raised on the dorsum of each animal. Group 1 was the control group, group 2 received 830 nm laser radiations, and group 3 was submitted to 670 nm laser radiation (power density=0.5 mW/cm(2)). The animals underwent laser therapy with 36 J/cm(2) energy density (total energy=2.52 J and 72 sec per session) immediately after surgery and on the 4 subsequent days. The application site of laser radiation was one point at 2.5 cm from the flap's cranial base. The percentage of skin flap necrosis area was calculated on the 7th postoperative day using the paper template method. A skin sample was collected immediately after to determine the vascular endothelial growth factor (VEGF) expression and the epidermal cell proliferation index (KiD67). RESULTS: Statistically significant differences were found among the percentages of necrosis, with higher values observed in group 1 compared with groups 2 and 3. No statistically significant differences were found among these groups using the paper template method. Group 3 presented the highest mean number of blood vessels expressing VEGF and of cells in the proliferative phase when compared with groups 1 and 2. CONCLUSIONS: LLLT was effective in increasing random skin flap viability in rats. The 670 nm laser presented more satisfactory results than the 830 nm laser.


Subject(s)
Low-Level Light Therapy/methods , Surgical Flaps/blood supply , Analysis of Variance , Animals , Lasers, Semiconductor , Male , Necrosis , Rats , Rats, Wistar , Tissue Survival
5.
Clinics (Sao Paulo) ; 67(2): 171-8, 2012.
Article in English | MEDLINE | ID: mdl-22358243

ABSTRACT

OBJECTIVES: The clinical significance of ischemia/reperfusion of the lower extremities demands further investigation to enable the development of more effective therapeutic alternatives. This study investigated the changes in the vascular reactivity of the rabbit femoral artery and nitric oxide metabolites under partial ischemia/ reperfusion conditions following cilostazol administration. METHODS: Ischemia was induced using infrarenal aortic clamping. The animals were randomly divided into seven groups: Control 90 minutes, Ischemia/Reperfusion 90/60 minutes, Control 120 minutes, Ischemia/Reperfusion 120/90 minutes, Cilostazol, Cilostazol before Ischemia/Reperfusion 120/90 minutes, and Ischemia 120 minutes/Cilostazol/ Reperfusion 90 minutes. Dose-response curves for sodium nitroprusside, acetylcholine, and the calcium ionophore A23187 were obtained in isolated femoral arteries. The levels of nitrites and nitrates in the plasma and skeletal muscle were determined using chemiluminescence. RESULTS: Acetylcholine-and A23187-induced relaxation was reduced in the Ischemia/Reperfusion 120/90 group, and treatment with cilostazol partially prevented this ischemia/reperfusion-induced endothelium impairment. Only cilostazol treatment increased plasma levels of nitrites and nitrates. An elevation in the levels of nitrites and nitrates was observed in muscle tissues in the Ischemia/Reperfusion 120/90, Cilostazol/Ischemia/Reperfusion, and Ischemia/ Cilostazol/Reperfusion groups. CONCLUSION: Hind limb ischemia/reperfusion yielded an impaired endothelium-dependent relaxation of the femoral artery. Furthermore, cilostazol administration prior to ischemia exerted a protective effect on endothelium-dependent vascular reactivity under ischemia/reperfusion conditions.


Subject(s)
Femoral Artery/drug effects , Ischemia/prevention & control , Nitric Oxide/blood , Reperfusion Injury/prevention & control , Tetrazoles/administration & dosage , Vasodilator Agents/administration & dosage , Animals , Cilostazol , Disease Models, Animal , Hindlimb/blood supply , Ischemia/chemically induced , Ischemia/metabolism , Male , Rabbits , Random Allocation , Reperfusion Injury/chemically induced , Reperfusion Injury/metabolism
6.
Clinics ; 67(2): 171-178, 2012. ilus, graf, tab
Article in English | LILACS | ID: lil-614642

ABSTRACT

OBJECTIVES: The clinical significance of ischemia/reperfusion of the lower extremities demands further investigation to enable the development of more effective therapeutic alternatives. This study investigated the changes in the vascular reactivity of the rabbit femoral artery and nitric oxide metabolites under partial ischemia/ reperfusion conditions following cilostazol administration. METHODS: Ischemia was induced using infrarenal aortic clamping. The animals were randomly divided into seven groups: Control 90 minutes, Ischemia/Reperfusion 90/60 minutes, Control 120 minutes, Ischemia/Reperfusion 120/90 minutes, Cilostazol, Cilostazol before Ischemia/Reperfusion 120/90 minutes, and Ischemia 120 minutes/Cilostazol/ Reperfusion 90 minutes. Dose-response curves for sodium nitroprusside, acetylcholine, and the calcium ionophore A23187 were obtained in isolated femoral arteries. The levels of nitrites and nitrates in the plasma and skeletal muscle were determined using chemiluminescence. RESULTS: Acetylcholine-and A23187-induced relaxation was reduced in the Ischemia/Reperfusion 120/90 group, and treatment with cilostazol partially prevented this ischemia/reperfusion-induced endothelium impairment. Only cilostazol treatment increased plasma levels of nitrites and nitrates. An elevation in the levels of nitrites and nitrates was observed in muscle tissues in the Ischemia/Reperfusion 120/90, Cilostazol/Ischemia/Reperfusion, and Ischemia/ Cilostazol/Reperfusion groups. CONCLUSION: Hind limb ischemia/reperfusion yielded an impaired endothelium-dependent relaxation of the femoral artery. Furthermore, cilostazol administration prior to ischemia exerted a protective effect on endotheliumdependent vascular reactivity under ischemia/reperfusion conditions.


Subject(s)
Animals , Male , Rabbits , Femoral Artery/drug effects , Ischemia/prevention & control , Nitric Oxide/blood , Reperfusion Injury/prevention & control , Tetrazoles/administration & dosage , Vasodilator Agents/administration & dosage , Disease Models, Animal , Hindlimb/blood supply , Ischemia/chemically induced , Ischemia/metabolism , Random Allocation , Reperfusion Injury/chemically induced , Reperfusion Injury/metabolism
8.
J Surg Res ; 164(1): 139-45, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20739032

ABSTRACT

BACKGROUND: Ischemia-reperfusion injury is believed to be a major cause of transferred skin flap failure. Cigarette smoking is known to be associated with endogenous antioxidant depletion, hypercoagulability, and cutaneous vasoconstriction. This investigation was carried out to study possible effects of pentoxyfilline or heparin on rat skin reperfusion injury under tobacco exposure. MATERIALS AND METHODS: Thirty-six rats were randomized into two major groups: 18 were exposed to cigarette smoke during a 4 wk period prior to surgery; the remaining 18 underwent a sham smoking procedure. Each group was further divided into three equal subgroups: heparin, pentoxyfilline, and saline solution. One identical skin flap was raised in each animal. The vasculature of the flap was clamped for 3 h and reperfused for 5 min. A venous blood sample was obtained from the flap after reperfusion for serum malondialdehyde (MDA) and myeloperoxidase (MPO) analysis. Flap survival was assessed 7 d after the procedure. RESULTS: The lipid peroxidation levels and flap necrosis were significantly higher in the cigarette-smoking group skin flaps. There was also a decrease of MPO activity in this group compared with the non-smoking group. Heparin-treated rats had significantly lower MDA levels and showed the most viable percent area among smoking rats. CONCLUSIONS: These data suggest that heparin had a significant beneficial effect both on flap survival and on the lipid peroxidation reduction after smoke exposure in the rat axial-pattern skin flap subjected to ischemia and reperfusion injury. Pharmacologic therapy may represent an alternative way to counteract tobacco effects in flap surgery in emergency situations.


Subject(s)
Heparin/pharmacology , Pentoxifylline/pharmacology , Reperfusion Injury/drug therapy , Skin/drug effects , Surgical Flaps/pathology , Tobacco Smoke Pollution/adverse effects , Animals , Anticoagulants/pharmacology , Dermatologic Surgical Procedures , Drug Therapy, Combination , Free Radical Scavengers/pharmacology , Male , Malondialdehyde/blood , Necrosis , Oxidative Stress/drug effects , Peroxidase/blood , Rats , Rats, Wistar , Skin/blood supply , Surgical Flaps/blood supply , Vasoconstriction/drug effects , Vasoconstriction/physiology
9.
Scand J Trauma Resusc Emerg Med ; 18: 41, 2010 Jul 19.
Article in English | MEDLINE | ID: mdl-20642850

ABSTRACT

BACKGROUND: The supraceliac aortic cross-clamping can be an option to save patients with hipovolemic shock due to abdominal trauma. However, this maneuver is associated with ischemia/reperfusion (I/R) injury strongly related to oxidative stress and reduction of nitric oxide bioavailability. Moreover, several studies demonstrated impairment in relaxation after I/R, but the time course of I/R necessary to induce vascular dysfunction is still controversial. We investigated whether 60 minutes of ischemia followed by 30 minutes of reperfusion do not change the relaxation of visceral arteries nor the plasma and renal levels of malondialdehyde (MDA) and nitrite plus nitrate (NOx). METHODS: Male mongrel dogs (n = 27) were randomly allocated in one of the three groups: sham (no clamping, n = 9), ischemia (supraceliac aortic cross-clamping for 60 minutes, n = 9), and I/R (60 minutes of ischemia followed by reperfusion for 30 minutes, n = 9). Relaxation of visceral arteries (celiac trunk, renal and superior mesenteric arteries) was studied in organ chambers. MDA and NOx concentrations were determined using a commercially available kit and an ozone-based chemiluminescence assay, respectively. RESULTS: Both acetylcholine and calcium ionophore caused relaxation in endothelium-intact rings and no statistical differences were observed among the three groups. Sodium nitroprusside promoted relaxation in endothelium-denuded rings, and there were no inter-group statistical differences. Both plasma and renal concentrations of MDA and NOx showed no significant difference among the groups. CONCLUSION: Supraceliac aortic cross-clamping for 60 minutes alone and followed by 30 minutes of reperfusion did not impair relaxation of canine visceral arteries nor evoke biochemical alterations in plasma or renal tissue.


Subject(s)
Aorta, Abdominal/surgery , Arteries/physiology , Ischemia , Reperfusion , Surgical Procedures, Operative , Vasodilation/physiology , Animals , Arteries/surgery , Constriction , Dogs , Male , Outcome Assessment, Health Care , Random Allocation , Reperfusion Injury/etiology
10.
J Biomed Sci ; 16: 45, 2009 May 05.
Article in English | MEDLINE | ID: mdl-19416519

ABSTRACT

Segments of the canine internal mammary artery (35 mm in length) were suspended in vitro in an organ chamber containing physiological salt solution (95% O2/5% CO2, pH = 7.4, 37 degrees C). Segments were individually cannulated and perfused at 5 ml/minute using a roller pump. Vasorelaxant activity of the effluent from the perfused internal mammary arteries was bioassayed by measuring the decrease in tension induced by the effluent of the coronary artery endothelium-free ring which had been contracted with prostaglandin F2alpha (2 x 10(-6) M). Intraluminal perfusion of adenosine diphosphate (10(-5) M) induced significant increase in relaxant activity in the effluent from the perfused blood vessel. However, when adenosine diphosphate (10(-5) M) was added extraluminally to the internal mammary artery, no change in relaxant activity in the effluent was noted. In contrast, acetylcholine produced significant increase in the relaxant activity on the effluent of the perfused internal mammary artery with both intraluminal and extraluminal perfusion. The intraluminal and extraluminal release of endothelium-derived relaxing factor (EDRF) by acetylcholine (10(-5) M) can be inhibited by site-specific administration of atropine (10(-5) M). These experiments indicate that certain agonists can induce the release of EDRF only by binding to intravascular receptors while other agonists can induce endothelium-dependent vasodilatation by acting on neural side receptors.


Subject(s)
Acetylcholine/pharmacology , Adenosine Diphosphate/pharmacology , Mammary Arteries/drug effects , Vasodilator Agents/pharmacology , Animals , Coronary Vessels/drug effects , Coronary Vessels/physiology , Dogs , Endothelium, Vascular/drug effects , Endothelium, Vascular/physiology , Female , Male , Vasodilation/drug effects
11.
J Surg Res ; 153(2): 254-62, 2009 May 15.
Article in English | MEDLINE | ID: mdl-18755481

ABSTRACT

BACKGROUND/AIMS: Nuclear factor kappa B (NFkappaB) plays important role in the pathogenesis of skeletal muscle ischemia/reperfusion (I/R) injury. Caffeic acid phenyl ester (CAPE), a potent NFkappaB inhibitor, exhibits protective effects on I/R injury in some tissues. In this report, the effect of CAPE on skeletal muscle I/R injury in rats was studied. METHODS: Wistar rats were submitted to sham operation, 120-min hindlimb ischemia, or 120-min hindlimb ischemia plus saline or CAPE treatment followed by 4-h reperfusion. Gastrocnemius muscle injury was evaluated by serum aminotransferase levels, muscle edema, tissue glutathione and malondialdehyde measurement, and scoring of histological damage. Apoptotic nuclei were determined by a terminal uridine deoxynucleotidyl transferase dUTP nick end labeling assay. Muscle neutrophil and mast cell accumulation were also assessed. Lipoperoxidation products and NFkappaB were evaluated by 4-hydroxynonenal and NFkappaB p65 immunohistochemistry, respectively. RESULTS: Animals submitted to ischemia showed a marked increase in aminotransferases after reperfusion, but with lower levels in the CAPE group. Tissue glutathione levels declined gradually during ischemia to reperfusion, and were partially recovered with CAPE treatment. The histological damage score, muscle edema percentage, tissue malondialdehyde content, apoptosis index, and neutrophil and mast cell infiltration, as well as 4-hydroxynonenal and NFkappaB p65 labeling, were higher in animals submitted to I/R compared with the ischemia group. However, the CAPE treatment significantly reduced all of these alterations. CONCLUSIONS: CAPE was able to protect skeletal muscle against I/R injury in rats. This effect may be associated with the inhibition of the NFkappaB signaling pathway and decrease of the tissue inflammatory response following skeletal muscle I/R.


Subject(s)
Caffeic Acids/therapeutic use , Muscle, Skeletal/injuries , NF-kappa B/antagonists & inhibitors , Phenylethyl Alcohol/analogs & derivatives , Reperfusion Injury/drug therapy , Animals , Caffeic Acids/pharmacology , Male , Medicine, Traditional , Phenylethyl Alcohol/pharmacology , Phenylethyl Alcohol/therapeutic use , Rats , Rats, Wistar
12.
Int J Angiol ; 18(3): 119-25, 2009.
Article in English | MEDLINE | ID: mdl-22477511

ABSTRACT

Thromboangiitis obliterans (TAO) is a segmental inflammatory occlusive disorder that affects small- and medium-sized arteries, and arm and leg veins of young smokers. Several different diagnostic criteria have been offered for the diagnosis of TAO. Clinically, it manifests as migratory thrombophlebitis or signs of arterial insufficiency in the extremities. It is characterized by highly cellular and inflammatory occlusive thrombi, primarily of the distal extremities. Thromboses are often occlusive and sometimes display moderate, nonspecific inflammatory infiltrate, consisting mostly of polymorphonuclear leukocytes, mononuclear cells and rare multinuclear giant cells. The immune system appears to play a critical role in the etiology of TAO. However, knowledge about immunological aspects involved in the progression of vascular tissue inflammation, and consequently, the evolution of this disease, is still limited. There are several studies that suggest the involvement of genetic factors and results have shown increasing levels of antiendothelial cell antibodies in patients with active disease. Vasodilation is impaired in patients with TAO. TAO disorder may actually be an autoimmune disorder, probably initiated by an unknown antigen in the vascular endothelium, possibly a component of nicotine. There are various therapies available for treatment of TAO, but the major and indispensable measure is smoking cessation. Except for discontinuation of tobacco use, no forms of therapy are definitive. Sympathectomy, cilostazol and prostaglandin analogues (prostacyclin or prostaglandin E) have been used in specific conditions. Recently, therapeutic angiogenesis with autologous transplantation of bone marrow mononuclear cells has been studied in patients with critical limb ischemia.

13.
Ann Vasc Surg ; 21(5): 618-28, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17823044

ABSTRACT

The aim of the investigation was to study the possible effects of in vivo infusion of nitric oxide (NO) blockers upon the in vitro endothelium-dependent femoral reactivity. The experimental model tested herein was the inferior canine hindlimb global ischemia induced by infrarenal abdominal aortic cross-clamping followed by reperfusion. The NO blockers employed in the tests were N(G)-nitro-l-arginine methyl ester (L-NAME), aminoguanidine (AMG), and methylene blue (MB), which were infused immediately after the anesthesia induction. The research protocol was standardized in two main experimental groups, control and ischemia/reperfusion (I/R) injury, randomized in eight subgroups including controls and NO blockers. The femoral artery vascular reactivity was studied in vitro with the aid of a setup consisting of eight organ chambers, where segments of 4-5 mm were suspended and connected to force transducers in the presence of indomethacin to block the cyclooxygenase pathway. The NO-release pathway was evaluated by using specific pharmacological agonists in the in vitro experiments. The L-NAME in vivo infusion led to in vitro endothelium dysfunction in both groups and was associated with high mortality in the animals submitted to I/R. AMG and MB, two clinically used drugs, did not cause in vitro endothelium dysfunction in either of the two groups, which gives evidence that these drugs are not deleterious in the milieu of I/R injury. Nitrite/nitrate plasma levels were not significant except for the L-NAME groups, which presented significant NO decrease.


Subject(s)
Endothelium-Dependent Relaxing Factors/antagonists & inhibitors , Femoral Artery/drug effects , Hindlimb/blood supply , Ischemia/physiopathology , Nitric Oxide Synthase/antagonists & inhibitors , Nitric Oxide/antagonists & inhibitors , Reperfusion , Animals , Cyclooxygenase Inhibitors/pharmacology , Dogs , Endothelium, Vascular/drug effects , Enzyme Inhibitors/pharmacology , Female , Femoral Artery/physiopathology , Guanidines/pharmacology , Indomethacin/pharmacology , Male , Methylene Blue/pharmacology , Muscle, Smooth, Vascular/drug effects , NG-Nitroarginine Methyl Ester/pharmacology , Nitrates/blood , Nitric Oxide/agonists , Nitrites/blood , Random Allocation , Reperfusion Injury/physiopathology , Vasodilator Agents/pharmacology
14.
Cardiovasc Ultrasound ; 4: 32, 2006 Aug 17.
Article in English | MEDLINE | ID: mdl-16914059

ABSTRACT

BACKGROUND: To establish the correlation between quantitative analysis based on B-mode ultrasound images of vulnerable carotid plaque and histological examination of the surgically removed plaque, on the basis of a videodensitometric digital texture characterization. METHODS: Twenty-five patients (18 males, mean age 67 +/- 6.9 years) admitted for carotid endarterectomy for extracranial high-grade internal carotid artery stenosis (> or = 70% luminal narrowing) underwent to quantitative ultrasonic tissue characterization of carotid plaque before surgery. A computer software (Carotid Plaque Analysis Software) was developed to perform the videodensitometric analysis. The patients were divided into 2 groups according to symptomatology (group I, 15 symptomatic patients; and group II, 10 patients asymptomatic). Tissue specimens were analysed for lipid, fibromuscular tissue and calcium. RESULTS: The first order statistic parameter mean gray level was able to distinguish the groups I and II (p = 0.04). The second order parameter energy also was able to distinguish the groups (p = 0,02). A histological correlation showed a tendency of mean gray level to have progressively greater values from specimens with < 50% to > 75% of fibrosis. CONCLUSION: Videodensitometric computer analysis of scan images may be used to identify vulnerable and potentially unstable lipid-rich carotid plaques, which are less echogenic in density than stable or asymptomatic, more densely fibrotic plaques.


Subject(s)
Carotid Stenosis/diagnosis , Densitometry , Image Processing, Computer-Assisted , Ultrasonography , Aged , Calcium/metabolism , Carotid Arteries/metabolism , Carotid Arteries/pathology , Carotid Stenosis/metabolism , Carotid Stenosis/pathology , Densitometry/methods , Female , Humans , Image Processing, Computer-Assisted/standards , Lipid Metabolism , Male , Middle Aged , Observer Variation , Video Recording
15.
Microsurgery ; 26(6): 456-64, 2006.
Article in English | MEDLINE | ID: mdl-16924631

ABSTRACT

The objective of the present investigation was to compare the effect of isovolemic hemodilution with 3% albumin, dextran-40, and enoxaparin on the prevention of thrombosis in femoral vein microanastomosis using an experimental model in rats. Forty male Wistar rats were allocated into four groups: group 1, control, thrombogenic model without previous treatment; group 2, hemodiluted, thrombogenic model with previous hemodilution; group 3, dextran-40, thrombogenic model with dextran infusion (10 ml/kg), and group 4, enoxaparin, thrombogenic model with administration of enoxaparin (0.5 mg/kg/day). Hemostatic parameters, hematologic examinations, patency of anastomosis, and histopathological examination were evaluated. The hemostatic parameters were similar in the four groups studied. Group hemodiluted, dextran-40, and enoxaparin showed significantly reduced number of red blood cells and platelets as compared with the control group. The hemodilution significantly increased the patency rates of the vein at 20 min and 48 h. Dextran-40 and enoxaparin improved the patency of the vein only at 20 min, but failed to show a significant increase in the final patency at 48 h. After 48 h, the rate of venous thrombosis, as evaluated microscopically, was significantly decreased in hemodiluted animals (1/8) as compared with controls (10/10); in rats treated with dextran-40 (7/10) and enoxaparin (5/10) the rate of venous thrombosis was significantly higher as compared with rats of the group hemodiluted. Based on these observations, it can be concluded that hemodilution with albumin 3% was a safe and more adequate procedure than the use of the schemes of administration of dextran-40 and enoxaparin used in this study to prevent thrombus formation at femoral vein microanastomosis in rats. Since hemodilution promotes reduction in blood viscosity and in erythrocyte and platelet aggregation as well as dilution of the coagulation factors themselves, its use could provide better microcirculatory blood perfusion, decreasing the risk of thrombosis, and making possible safer microsurgical procedures.


Subject(s)
Dextrans/therapeutic use , Enoxaparin/therapeutic use , Femoral Vein/surgery , Hemodilution/methods , Postoperative Complications/prevention & control , Serum Albumin, Bovine/therapeutic use , Venous Thrombosis/prevention & control , Anastomosis, Surgical/adverse effects , Animals , Dextrans/administration & dosage , Disease Models, Animal , Drug Therapy, Combination , Enoxaparin/administration & dosage , Fibrinolytic Agents/administration & dosage , Fibrinolytic Agents/therapeutic use , Infusions, Intravenous , Male , Microsurgery/adverse effects , Microsurgery/methods , Plasma Substitutes/administration & dosage , Plasma Substitutes/therapeutic use , Rats , Rats, Wistar , Serum Albumin, Bovine/administration & dosage , Treatment Outcome , Venous Thrombosis/etiology
16.
Exp Cell Res ; 309(2): 340-4, 2005 Oct 01.
Article in English | MEDLINE | ID: mdl-16018999

ABSTRACT

Mesenchymal stem cells (MSC) can be isolated from many sites adults and the fetus. Cells with osteoblastic, chondrogenic, leiomiogenic and stromogenic potentials have been obtained from the bovine artery wall, and we now show that MSC can be isolated also from the adult human vein wall. Cells detached from internal surface of the saphenous vein are cultured in vitro for 2-3 weeks and replated weekly. The culture forms a semi-confluent layer of spindle-shaped cells that are CD13(+), CD29(+), CD44(+), CD34(-), CD45(-), CD14(-), CD133(-), CD31(-), CD33(-), CD54(+), CD106(-), CD90(+), KDR(-), cadherin-5-, HLA class I(+) and HLA-DR- and differentiate in vitro into osteoblasts, chondrocytes and adipocytes. Gene expression, when compared with seven other normal tissues, shows strong similarity with MSC obtained from other sources. Three genes more expressed in saphenous MSC than in the other two MSC are related to angiogenesis, and the expression of two of them is shared by endothelial cells. These results demonstrate that the human vein wall contains mesenchymal cells with morphologic features, immunophenotypic markers, gene expression profile and differentiation potential that are similar to MSC obtained from the bone marrow and from the umbilical vein.


Subject(s)
Mesenchymal Stem Cells/cytology , Saphenous Vein/cytology , Varicose Veins , Cell Adhesion , Cell Culture Techniques/methods , Cell Lineage , Cells, Cultured , Humans , Mesenchymal Stem Cells/physiology , Osteonectin/genetics , Osteonectin/metabolism , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction
17.
Shock ; 23(6): 582-7, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15897814

ABSTRACT

In this study, the isolated use of methylene blue (MB) in the treatment of anaphylactic shock induced by Compound 48/80 (C48/80), a potent histamine releaser, was examined, and the study of the effects of MB on the function of the aorta artery endothelium was accomplished in vitro. MB was used in a single 3.0 mg/kg dose, and C48/80 was used in a single 4.5 mg/kg dose. The study protocol included the following experimental groups, containing six animals each: group I (control), animals in the absence of any drug action; group II (MB), MB infusion; Group III (C48/80), anaphylactic shock induced by using C48/80; group IV (C48/80 + MB), anaphylactic shock treated with MB infusion at the moment of major hypotension; and group V (MB + C48/80), prevention of anaphylactic shock with MB by means of MB infusion minutes before the 4.5 mg/kg C48/80 infusion. Nitric oxide plasma levels were measured in each of the experimental groups. After the in vivo studies were performed, an in vitro study was conducted using segments of the abdominal aortas of the rabbits to determine the effect of MB on the arterial endothelium. The results obtained in the present investigation have shown that MB intravenous infusion does not change the mean arterial pressure when compared with the control group (n = 6 in each group, P < 0.05); that C48/80 is effective in producing experimental anaphylactic shock (n = 6, P < 0.05); that the attempt to prevent anaphylactic shock with MB results in a mean prolongation of animal survival ranging from 17 to 34 min (n = 6 in each group, P < 0.05); that MB is effective in reversing anaphylactic shock in all the studied rabbits (n = 6, P < 0.05); that absolute and percentage plasma nitrate values obtained with the experimental groups do not differ (n = 6, each group, P < 0.05); and that the in vitro study of segments of abdominal aorta has shown that there has not been endothelial dysfunction in any of the groups (n = 6 in each group, P < 0.05). The good results obtained in this study open a research path that may offer data to define new paradigms for treating anaphylaxis.


Subject(s)
Anaphylaxis/complications , Anaphylaxis/drug therapy , Methylene Blue/pharmacology , p-Methoxy-N-methylphenethylamine/toxicity , Adrenal Cortex Hormones/metabolism , Animals , Arteries/pathology , Blood Pressure , Dose-Response Relationship, Drug , Endothelium, Vascular/cytology , Endothelium, Vascular/pathology , Enzyme Inhibitors/pharmacology , Epinephrine/metabolism , Hypotension , Male , Nitrates/blood , Nitric Oxide/blood , Nitric Oxide/metabolism , Nitrites/blood , Rabbits , Time Factors
18.
Vasc Endovascular Surg ; 39(1): 39-46, 2005.
Article in English | MEDLINE | ID: mdl-15696247

ABSTRACT

This experimental investigation was carried out to study the endothelium-dependent ischemia-reperfusion injury upon the release of nitric oxide (NO) in the canine femoral artery. The tested experimental model was the inferior canine hindlimb ischemia induced by infrarenal abdominal aortic clamping followed by reperfusion. The research protocol was standardized in four experimental groups (n=6): (1) Control group; (2) Ischemia (120 minutes) group; (3) Ischemia (90 minutes) and reperfusion (60 minutes) group; and (4) Ischemia (120 minutes) and reperfusion (90 minutes) group. The femoral artery vascular reactivity was studied in vitro with the aid of an eight "organ chambers'' setup, where segments from 4 to 5 mm, with and without endothelium, were suspended and connected to force transducers. The fundamental data of this study were as follows: (1) Ischemia caused by 120 minutes of infrarenal aortic clamping did not cause femoral artery endothelium dysfunction. (2) Ischemia caused by 90 minutes of clamping followed by 60 minutes of reperfusion also did not cause endothelium dysfunction, with an observed tendency to signal transduction impairment (studied by the sodium fluoride dose response curves). (3) Ischemia caused by 120 minutes of clamping followed by 90 minutes of reperfusion caused endothelium dysfunction, observed by the femoral artery impaired capacity of the endothelium-dependent NO release evoked by acetylcholine, adenosine diphosphate, and sodium fluoride. The present pharmacologic in vitro observations are concordant with the evidence that the NO-release impairment, caused by inferior canine hindlimb ischemia followed by reperfusion, is a consequence of endothelium cell membrane receptors, and G-proteins signal transduction dysfunction.


Subject(s)
Reperfusion Injury/complications , Vascular Diseases/metabolism , Vasodilation/physiology , Animals , Dogs , Female , Femoral Artery/metabolism , Femoral Artery/physiopathology , Hindlimb/blood supply , In Vitro Techniques , Male , Models, Animal , Nitric Oxide/biosynthesis , Receptors, Cell Surface/physiology , Signal Transduction/physiology , Vascular Diseases/etiology , Vascular Diseases/physiopathology
20.
Microsurgery ; 24(3): 194-9, 2004.
Article in English | MEDLINE | ID: mdl-15160377

ABSTRACT

The great resistance of muscle to ischemia was used to study blood flow-dependent phenomena produced by anesthetic drugs in this condition. A short reperfusion period was used in order to favor metabolic changes indicative of an effect of chlorpromazine (CPZ) on blood flow. Gracilis muscles of dogs were submitted to 5 h of ischemia and 30 min of reperfusion. CPZ-treated animals were injected I.V. (2 mg/kg) 10 min before the beginning of ischemia. Biopsies provided the material for tissue measurements. Lactate content and pH were determined in blood samples collected from a muscle efferent vein. In both the CPZ-treated and nontreated groups, ischemia induced a decline in muscle glycogen content, with a corresponding increase in muscle lactate and a decrease in mitochondrial respiratory control ratio. After 30 min of reperfusion, tissue levels of lactate did not attain preischemic values but showed a clear decline in the two experimental groups, evidencing the reversible state of the muscle. All other metabolic parameters remained unchanged. Mitochondrial respiratory control remained functional during ischemia and reperfusion. Blood pH displayed similar changes in both groups. There was no metabolic indication that the drug affected blood flow during early reperfusion and/or of a greater sensitivity of muscle endothelial cells to anesthetic drugs.


Subject(s)
Chlorpromazine/pharmacology , Ischemia/drug therapy , Mitochondria, Muscle/metabolism , Muscle, Skeletal/blood supply , Reperfusion Injury/metabolism , Animals , Disease Models, Animal , Dogs , Glycogen/metabolism , Hydrogen-Ion Concentration , Ischemia/therapy , Lactates/metabolism , Mitochondria, Muscle/drug effects , Muscle Contraction/drug effects , Muscle Contraction/physiology , Muscle, Skeletal/metabolism , Musculoskeletal Physiological Phenomena , Reference Values
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