Varicose veins - Wikipedia VARICOSITY (Latin varix, varicis swelling on veins) — the change of veins which is characterized by uneven increase in their gleam with formation of protrusions in a zone of the thinned venous wall, the distorted course of vessels with development of their nodularlike crimpiness, functional insufficiency of valves and the perverted blood-groove.


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We offer a unique range of organic Viscosity Probes Molecular Rotorsideal for microscopy, such as bei varicosity Probe spatial imaging of microviscosity within individual domains within live cells, as well as for a great many other applications in the Life and Physical Sciences. Ursa BioScience's approach is based upon the detection of fluorescence from unique fluorescent molecules, bei varicosity Probe Molecular Rotors, which show a strong fluorescence response in both lifetime and emission spectra to the viscosity of the surrounding environment.

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The excitation wavelength was nm. The excitation wavelength was nm and the emission observed through a monochromator centered at nm. Note that the instrumental response function irfrecorded from a scattering solution, also is shown in black. The data can be analyzed Su Jok Therapie Varizen terms of a bi-exponential decay model with bei varicosity Probe parameters shown in the table.

B Peak riboslim apotheke intensity observed in panel A bei varicosity Probe as function of glycerol viscosity.

The data can be analyzed in terms of a mono-exponential decay model with recovered parameters shown in the table. At 20 C the lifetime is bi-exponential in glycerol0. At 50 C the lifetimes are much shorter, 0. B Peak bei varicosity Probe intensity plotted as function of glycerol viscosity.

It can be readily excited at nm with an emission centred in the green around nm. B Peak fluorescence intensity as seen in panel A plotted as function of glycerol viscosity. It can be readily excited from nm, with an emission centred around nm. Bei varicosity Probe fluorophore can also be used to characterize aggregation state of lipophilic molecules, e. The exciation wavelength was nm. The accessibility of the dark non-emissive TICT state is typically responsible for the non-radiative decay pathways in a http://pattern-lab.de/tysuwubidemim/varizen-fussmassage.php, which can be altered via viscosity, giving rise to the viscosity dependence observed [2].

Panel A and B shows the same data but on different scales. Note that the peak emission intensities are normalized, i. B Peak emission intensity observed in panel A plotted bei varicosity Probe function of glycerol viscosity. Time-resolved fluorescence decays recorded for DCVJ dissolved in glycerol at different temperatures. Note that bei varicosity Probe instrument response function irf recorded from a scattering solution also is shown.

The table summarizes parameters obtained by fitting the data to biexponential or monoexponential decay models. A Absorbance spectra recorded for Viscous UV dissolved in methanol. A Emission spectra recorded for Viscous UV dissolved in glycerol at different temperatures. B Peak emission intensity, as recorded in panel A, bei varicosity Probe as function of glycerol viscosity.

At 50 C the lifetimes are shorter, 0. Note that the instrument response function irf recorded from a scattering solution also is shown The excitation wavelength was nm and the emission bei varicosity Probe through a bei varicosity Probe centered at nm. The table summarizes parameters obtained by fitting the data to a bi-exponential decay model. The emission is typically more pronounced in the more viscous the media and shows a linear response over the cP viscosity range.

Note that the water absorbance spectra is red shifted about 10 nm. B Peak intensity plotted as function of bei varicosity Probe viscosity. The excitation wavelength was nm and the emission recorded through a bei varicosity Probe centered at nm. Note that the instrument bei varicosity Probe function, irf, also is shown.

The table summarize results obtained by fitting the time-resolved data to a bi-exponential decay model. B Peak area plotted as function of glycerol bei varicosity Probe. As with all our viscosity probes, the emission intensity increases as the viscosity also increases.

B Contour emission graphs recorded for sample as shown in panel A. The bei varicosity Probe has been corrected for a background emission form the oil. B Bei varicosity Probe emission spectra as presented in panel A plotted as function of the viscosity of the oil measured in an independent experiment. Note that the instrumental response function also is shown, as recorded from a scattering solution. The excitation wavelength was bei varicosity Probe and the excitation and emission polarizers set to vertical and magic angle, respectively.

B results of fitting recorded decay data to a bi-exponential decay model. Physical Chemistry Chemical Physics, Theodorakis, Molecular rotors - fluorescent biosensors for viscosity and flow. Journal of the American Chemical Society, Journal of Physical Chemistry C, Sign up to get interesting news and updates delivered to your inbox. Emails are tailored for your individual scientific area of interest.

User Account Register Login. Home Probe Bei varicosity Probe Viscosity Probes. Non-Conjugatable Viscosity Probes We offer a unique range of organic Viscosity Probes Molecular Rotorsideal for microscopy, such as the spatial imaging of microviscosity within individual domains within live cells, as well as for a great many other applications in the Life and Physical Sciences.

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To test in vitro the constrictor and relaxation responsiveness of bei varicosity Probe diseased segments of human saphenous vein from patients with varicose vein disease. The vein segments were derived i from the inguinal saphenous vein valvularly incompetent and slightly dilated; tissue A bei varicosity Probe ii from the distal end of the lower leg just above the medial ankle competent; tissue B ; iii from a tributary to the long saphenous vein bei varicosity Probe below the knee dilated, incompetent and overtly varicose; tissue C.

Relaxant responses were tested with acetylcholine and sodium nitroprusside. Both contractile agents contracted vein segments from the inguinal and ankle area with similar potency and efficacy, but were virtually without effect in the overtly varicose segments from the calf.

Acetylcholine-induced relaxation was similar for vein segments from locations A and B, bei varicosity Probe sodium nitroprusside was more effective in tissue B than A. These findings support the bei varicosity Probe that abnormalities within the venous wall affect venous smooth muscle bei varicosity Probe. Since competent and incompetent clinically normal vessels show normal contractile responses, whereas varicose vessels are not responsive to vasoactive drugs, it is likely that pharmacological treatment regimens are effective in early, but not in late stages of the disease.

Varicose veins of the lower limb affect a sizable fraction of the adult population and result in considerable suffering and bei varicosity Probe losses to the economy. Dilated veins bei varicosity Probe incompetent valves are the common manifestation of the disease. The consequence of the resultant reflux is a high venous pressure bei varicosity Probe venous hypertensive microangiopathy. Phleboedema, induration of the tissue in the distal leg, thrombophlebitis and ulcerations are common complications continue reading untreated varicosity [ 2 ].

Acute manifestations, such as deep venous thrombosis and pulmonary embolism [ 3 ] are serious complications, and the chronic form of the disease results in high socioeconomic costs due to long hospitalization and work disability [ 4 ].

The aetiology of primary varicosity is still unknown. A recent theory suggests that a defective control of venous tone leads to dilatation and subsequent insufficiency.

The possible role of an imbalance between endothelial derived contracting and relaxing bei varicosity Probe was reported by our group [ 8 ]. Several drugs including flavonoids and horse chestnut seed extract aescin are currently used for short-term treatment of varicose vein disease, but whether they bei varicosity Probe venous tone as part of their mechanism of action is controversial [ 9 — 10 ].

Learn more here the present study we determined the in vitro reactivity of long saphenous vein derived from patients with varicose vein disease.

We hypothesized that the efficacy of drugs raising venous tone may depend on the severity of the disease as evident from clinical symptoms. Hence, we obtained vein segments from three anatomical locations of the same patient, i. Tissues were obtained from seven female patients mean age, 46 years with primary varicosity, hospitalized for surgical vein stripping.

All patients received bei varicosity Probe anaesthesia and consented to the removal and use of tissues as described below. Colour flow duplex imaging and ascending phlebography were used to identify venous reflux. All patients had an incompetent long saphenous vein up to the calf region, varicose tributaries and perforating veins.

The long saphenous vein in the ankle region was competent in all cases. Except for one case of breast cancer and one of struma, the women bei varicosity Probe devoid of major diseases, in particular none suffered from diabetes, hypertension, or vasculitis.

Four women had given birth to two children, and three women to one child; two of them were taking steroid contraceptives. Short pieces of tissue were carefully removed before starting the stripping procedure from three anatomical locations Figure 1: Tissue A was incompetent with little or no dilatation, tissue B was grossly nonvaricose, competent and appeared clinically normal, tissue C was always dilated, overtly varicose and incompetent.

In a few cases, tissue A was incompetent and the vein was enlarged and varicose; bei varicosity Probe were not included in group A but formed bei varicosity Probe separate group that is referred to in the text. Procurement bei varicosity Probe variously diseased vein tissues from 3 anatomical locations modified from [ 7 ].

Tissue A was a morphologically incompetent but nonvaricose segment of proximal long saphenous vein from the groin; tissue B, from distal long saphenous vein above the ankle, was clinically nonvaricose with competent valves; tissue C, from a tributary to the long saphenous vein in bei varicosity Probe calf, was always overtly varicose and tortuous. Care was taken bei varicosity Probe to damage bei varicosity Probe endothelium.

Isotonic changes in length were measured by a mechano-electronic transducer and continuously recorded on Watanabe Multicorders Hugo Sachs-Elektronik, Freiburg, Germany. Phenylephrine was added to equilibrated tissues in individual doses to give final bath concentrations of 0.

After the last dose, acetylcholine 0. The agonists were removed by repeated washes with Krebs-Henseleit buffer until the baseline length of strips was regained. The experiments with sodium nitroprusside were done separately. We have found repeatedly that the addition of angiotensin II to U gives a quicker and more stable contraction than the bei varicosity Probe mimetic alone.

The mean bei varicosity Probe contraction bei varicosity Probe not different between groups A and B, but was significantly smaller in group C see Table 1.

All strips from group A contracted to depolarization by excess KCl at the end of experiment and were included in the analysis. The decision was based on the observation that in both cases, at least one adjacent B strip showed normal contractility, excluding the possibility that the vessel was already functionally defective before excision. All strips of group C were included most of them showed no contraction, see Results.

The experimental curves were fitted nonlinearly to the Hill equation describing log-linear concentration-response curves [ 12 ]. All other chemicals were of standard grade. Phenylephrine contracted veins from the inguinal tissue A and ankle area tissue B with similar potency and efficacy, but was virtually without effect in the overtly varicose segments from the calf tissue C Figure 2.

The corresponding E C 50 and maximum effect values derived from go here curve fits are listed in Bei varicosity Probe 1. Occasionally, the source saphenous vein of bei varicosity Probe groin area showed signs of valvular incompetence and the vein wall was thinned.

The reactivity of these tissues toward phenylephrine was similar to that of tissues A E C Likewise, a greatly varicose tributary to the long saphenous vein in the groin area was similarly reactive E C The contractile effect of aescin is shown in Figure 3.

The glycoside contracted strips A and B to a similar extent, but its potency was significantly higher in varicose than nonvaricose vein factor: The reactivity of bei varicosity Probe of overtly varicose veins was again close to zero Table 1.

Contractile and relaxant responses of lower limb bei varicosity Probe tissues from patients with primary varicosity. A, B, and C refer to the three anatomical locations shown in Figure 1. The contractile agents phenylephrine used to test acetylcholine relaxation and U plus angiotensin II used to test sodium nitroprusside relaxation were effective in all tissues from locations A and B, but generally not in tissue C, as expected from the results bei varicosity Probe phenylephrine and aescin see above.

Bei varicosity Probe precontraction, acetylcholine relaxed vein segments from the locations Bei varicosity Probe and B with similar potency and efficacy, and the respective E C 50 and E max values are also listed in Table 1. When added to saphenous vein segments from the groin that were more heavily diseased dilated and varicose; see section on patients and test groupsacetylcholine was similarly potent and efficacious as in tissues Verfahren zur Bewegungstherapie Krampfadern E C A few overtly varicose segments C contracted to the combination of U and angiotensin II 6 out of 24 stripsbut the maximum contraction was much less than in tissues B and C, preventing the quantification of sodium nitroprusside or acetylcholine bei varicosity Probe. In overtly bei varicosity Probe tributaries of human long saphenous vein vasomotion in response to contractile bei varicosity Probe relaxant stimuli is largely lost.

Vein segments from the groin and ankle region showed similar bei varicosity Probe, although the inguinal vessel was incompetent and the segment from the ankle was clinically healthy.

Therefore, it appears that pharmacological treatment regimens aimed at raising venous tone can be successful in early, but not late stages of the disease. There is general agreement that varicosity needs to be treated to prevent leg ulcers, and both surgical procedures and pharmacotherapy have long been used clinically. However, an important question is: To test the contractile response of the saphenous vein tissues we used the two agonists, phenylephrine bei varicosity Probe aescin.

The mechanism of action of which is not well understood [ 13 ]. The glycoside has link activity, prevents oedema formation by decreasing the permeability of the vessel wall for different low and high molecular weight plasma components [ 14 ] and exerts venoconstriction [ bei varicosity Probe ]. Both phenylephrine and aescin contracted tissues from the ankle bei varicosity Probe groin regions A and B, respectivelybut were virtually ineffective in the saphenous vein tributaries with overt tortuosities segments C.

Hence, venous return from the lower extremities becomes largely independent of vein size in such patients and probably depends mostly on skeletal muscle bei varicosity Probe. On the other hand, venoconstriction to the two agonists was intact in segments from the groin, indicating that phlebotonic drugs such as aescin may raise venous tone in segments that are morphologically still relatively little affected by the bei varicosity Probe, i.

This supports early intervention to prevent bei varicosity Probe progression of the disease. This contrasts bei varicosity Probe the present study, where we have used clinically healthy and varicose vein segments from the same patient.

Relaxation bei varicosity Probe the venous wall, even when caused by valvular insufficiency, aggravates venous stasis and oedema.

We have previously shown [ bei varicosity Probe ] that cultured endothelial cells from varicose veins derived from the inguinal area had a higher basal production of cGMP than cells derived from clinically healthy veins prepared for bypass surgery. Similarly, article source, an endothelium-independent relaxant in human saphenous vein, was more potent in relaxing diseased saphenous veins and the response to the agonist was greater in this tissue than in the clinically healthy control tissues from the bypass patients.

Individually or in combination these findings suggested stronger vascular relaxation in primary varicosity [ 8 ]. In the present study, we compared the relaxant response to sodium bei varicosity Probe and acetylcholine, wirksamste was Krampfadern das Mittel für endothelium-dependent agonist in human saphenous vein [ 17 — 18 ], in variously bei varicosity Probe tissues from the bei varicosity Probe patient.

Acetylcholine relaxed tissues A and B similarly, indicating that this agonist is unlikely to aggravate the early phase of varicosity, mainly characterized by the incompetence of the vessel tissue Bei varicosity Probe. In the final stage of the disease tissue Cboth contraction and bei varicosity Probe are lost.

In conclusion, the present findings further support the hypothesis that click within the venous wall bei varicosity Probe venous smooth muscle contractility.

Because both competent and incompetent clinically normal vessels show normal contractile responses, whereas Weide Tee mit Thrombophlebitis vessels no longer respond to vascular control, pharmacological treatment regimens may be successful in early, but not in the late stages of the disease.

Whether the observed loss of vasoconstrictor bei varicosity Probe is a cause or a sequel to the changes in the varicose vein wall requires additional investigation. The authors acknowledge the technical assistance of Mrs Birgit Jelinek-Fink.

This work was supported by the Austrian Research Fund, projects and to F. National Center for Biotechnology InformationU. Br J Clin Pharmacol. Received Bei varicosity Probe 12; Accepted Oct This article has been cited by other articles in PMC.

Abstract Aims To test in vitro the constrictor and relaxation responsiveness of variously diseased segments of human saphenous vein from bei varicosity Probe with varicose vein disease. Methods The vein segments were derived i from the inguinal bei varicosity Probe vein valvularly incompetent and slightly dilated; tissue A ; ii from the distal end of the lower leg just above the medial ankle competent; tissue B ; iii from a tributary to the long saphenous vein just below the knee dilated, incompetent and overtly varicose; tissue C.

Results Both contractile agents contracted vein segments from the inguinal and ankle area with similar potency and Dermatitis, Krampfadern, but were virtually without effect in the overtly varicose segments from the calf. Conclusions These findings support the notion that abnormalities within the venous wall affect venous smooth muscle contractility.

Introduction Varicose veins of the lower limb affect a sizable fraction of the adult population and result in considerable suffering and huge losses to the economy. Methods Bei varicosity Probe and test groups Tissues were obtained from seven female patients mean age, 46 years with Krampfadern geheilt Gras varicosity, hospitalized for surgical vein stripping. Open in a separate window. Experimental protocol Phenylephrine was added bei varicosity Probe equilibrated tissues in individual doses to give bei varicosity Probe bath concentrations of 0.

Exclusion criteria All strips from group A contracted to depolarization by excess KCl at the end of experiment and were included in the analysis. Results Phenylephrine contracted veins from the inguinal tissue A and ankle area tissue Strumpf Krampfadern with similar potency and efficacy, but was virtually without effect in the overtly varicose segments from the calf tissue C Figure 2.

Table 1 Contractile and relaxant responses of lower limb vein tissues from patients with primary varicosity. Discussion In overtly varicose tributaries of human long saphenous vein vasomotion in response to contractile and relaxant stimuli is largely lost.


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