{"id":94,"date":"2023-01-18T10:22:59","date_gmt":"2023-01-18T09:22:59","guid":{"rendered":"https:\/\/kurbel.org\/?page_id=94"},"modified":"2023-01-18T10:22:59","modified_gmt":"2023-01-18T09:22:59","slug":"reference-51-56","status":"publish","type":"page","link":"https:\/\/kurbel.org\/?page_id=94","title":{"rendered":"Reference 51-56"},"content":{"rendered":"\n<p><strong>Prof. Sven Kurbel MD, PhD \u2013 personal web pages<\/strong><br>Dept. of Physiology, Osijek Medical Faculty<br>J. Huttlera 4, 31000 Osijek, Croatia<br>e-mail: sven@jware.hr<\/p>\n\n\n\n<p><strong>51. Simulation model of defective insulin receptors as byproducts of receptor recycling.<br>Kurbel B, Kurbel S, Kristek Z, Jaki\u0107 M, Juri\u0107 M, Sulava D.<br>Med Hypotheses. 1997 Aug;49(2):165-70.<\/strong><\/p>\n\n\n\n<p>Department of Anaesthesiology, University Hospital Dubrava, Zagreb, Croatia.<\/p>\n\n\n\n<p>Our simulation model assumes that the defective insulin-binding receptors in<br>non-insulin-dependent diabetes (NIDDM) patients result from functional receptor<br>recycling. The model is a short program written in MS DOS 5.0 Qbasic. MODEL<br>DESIGN: Receptors with intracellular portions damaged in the process of recycling<br>are considered defective since they bind insulin but do mediate insulin effects,<br>or recycle. Their occurrence depends on the average activation rate of functional<br>receptors. The insulin-binding receptors (defective and functional) are objects<br>of slow and time-dependent turnover defined by the turnover rate. Recycled<br>receptors rejoin functional receptors or enter the pool of defective receptors.<br>The waste in the functional receptors\u2019 pool is covered by a limited amount of<br>newly synthesized receptors. The defective receptors often accumulate in cases of<br>increased activation of functional receptors. SIMULATION RESULTS: The<br>insulin-binding receptor quantity is determined, in the model, only by the number<br>of newly synthesized receptors, reflecting the intensity of insulin stimulation.<br>Synthesis is increased following variable insulin stimulations and decreased<br>after sustained, intensive insulin stimulation. The number of functional<br>receptors inversely reflects the average activation rate of functional receptors<br>compared with the insulin-binding receptors turnover rate. High activation rates<br>can diminish the proportion of functional receptors to less than 5% of that of<br>all insulin-binding receptors. The model predicts that cells bearing only<br>functional receptors show progressively shortened half-lives of receptors,<br>reflecting the receptor activation intensity. On the other hand, cells bearing<br>both defective and functional receptors show stable receptors\u2019 half-lives (20-36%<br>of the defective receptors\u2019 half-life). Simulation results suggest that reduced<br>functional receptor proportions in NIDDM patients might reflect the imbalance<br>between the activation of functional receptors and the slow catabolism of<br>defective receptors.<\/p>\n\n\n\n<p>PMID: 9278929&nbsp; [PubMed \u2013 indexed for MEDLINE]<\/p>\n\n\n\n<p><strong>52. Influence of subinhibitory concentrations of ceftazidime, ciprofloxacin and<br>azithromycin on the morphology and adherence of P-fimbriated escherichia coli.<br>Vranes J, Zagar Z, Kurbel S.<br>J Chemother. 1996 Aug;8(4):254-6<\/strong>0.<\/p>\n\n\n\n<p>Department of Microbiology and Parasitology, University of Zagreb, Medical<br>School, Croatia.<br><br>The influence of subinhibitory concentrations (1\/2, 1\/4, 1\/8, 1\/16 and 1\/32 x<br>MIC) of ceftazidime, ciprofloxacin and azithromycin on the morphology and<br>adherence of 29 wild-type P-fimbriated strains of Escherichia coli was studied.<br>Bacterial adherence to the Buffalo green monkey (BGM) cell line was tested before<br>and after treatment with antibiotics and detected by means of an<br>immunofluorescence staining. Significant dose dependent reduction of bacterial<br>adherence was observed, which correlated with the alterations in bacterial cell<br>morphology. After exposure of strains to sub-MICs of antibiotics, normal shapes,<br>spherical forms and filaments were noted. The greatest filamentation and the<br>greatest loss of adherence ability occurred at 1\/2 x MIC of ceftazidime.<br>Treatment with sub-MICs of ciprofloxacin resulted in shorter filaments, while<br>filamentation did not occur after bacterial exposure to sub-MICs of azithromycin.<br>Azithromycin was least damaging to the adherence ability of E. coli and at a<br>concentration of 1\/2 x MIC caused globoid cell formation.<br><br>PMID: 8873829&nbsp; [PubMed \u2013 indexed for MEDLINE]<\/p>\n\n\n\n<p><strong>53. Computer simulation of factors involved in the down-regulation of hormonal<br>effects.<br>Kurbel S, Kurbel B, Dici\u0107 M, Ugraji V.<br>Med Hypotheses. 1996 Mar;46(3):173-9.<\/strong><\/p>\n\n\n\n<p>Department of Oncology, Osijek Clinical Hospital.<br><br>Down-regulation of hormonal effects is in the presented simulation related to the<br>number of functional receptors and quantity of available hormonal stimulation.<br>The former is in the model substituted with the quantity of stimulation able to<br>produce a full down-regulation (Hs100) of target cells. The halftime (t1\/2) of<br>the hormonal effect recovery means the interval before the second hormonal<br>stimulation can elicit half of the initial hormonal effect. Recovered hormonal<br>effects are calculated after periods of two, three, four and five t1\/2. The<br>interval among hormonal stimulations varied from 1\/2 to 5\/2 of t1\/2. Shorter than<br>t1\/2 intervals showed profound down-regulation even at weak hormonal stimulations<br>(&gt; 20% of Hs100). Stable levels of hormonal effects after frequent hormonal<br>stimulations are found only in cases of very weak stimulations (&lt; 10% of Hs100).<br>Intervals equalling t1\/2 among weak stimulations (&lt; 20% Hs100) produced stable<br>hormonal effects. Further prolongation among repeated stimulations improved<br>stability of hormonal effects and even strong stimulations (&gt; 60% of Hs100) were<br>followed with only temporary profound down-regulation. Hormone-binding receptors<br>unable to activate target cells are in the model described as defective.<br>Probability for the target cell to be stimulated is in the model defined as P.<br>Relative quantity of hormonal stimulation per target cell needed to achieve<br>certain P is calculated for cells bearing different proportions of defective<br>receptors. Activation following weak hormone stimulations is highly probable (&gt;<br>90%) for cells bearing less than 30% of defective receptors. With the proportion<br>of defective receptors over 60%, the activation probability after weak hormone<br>stimulations is reduced (&lt; 66%). Down-regulation can be considered as a modulator<br>of hormonal effects. In prediabetic patients, intense stimulation of pancreatic<br>insulin secretion by frequent or increased ingestion of carbohydrates might lead<br>to sustained hyperinsulinemia. A substantial portion of the target tissue would<br>become down-regulated with increased number of defective insulin receptors. Poor<br>glucose utilization in the down-regulated tissue with resultant hyperglycemia<br>would further stimulate insulin secretion until failure. Reduced tissue<br>transportability of large hormone molecules, such as hGH, or proinsulin, can make<br>their effects more pronounced in the perivascular space. Circulating hormone<br>binding proteins or the basal membrane thickening in small vessels can further<br>decrease the hormonal effects on more remote cells. Physical activity in IDDM<br>patients increases insulin effect. Possible explanation is that increased muscle<br>perfusion is making more insulin available to the less down-regulated skeletal<br>muscle cells.<br><br>PMID: 8676750&nbsp; [PubMed \u2013 indexed for MEDLINE]<\/p>\n\n\n\n<p><strong>54. Mechanisms of prion diseases described as long-lasting disorders of the<br>blood-brain barrier system.<br>Kurbel S, Kurbel B.<br><\/strong><strong>Med Hypotheses. 1995 Dec;45(6):543-4.<\/strong><\/p>\n\n\n\n<p><br>Department of Oncology, Osijek Clinical Hospital, Croatia.<br><br>Prison diseases can be described as disorders wherein circulating prion molecules<br>of external origin intervene with the normal synthesis of similar molecules in<br>the central nervous system. The hypothesis is that the endogenous prion-like<br>molecules denote the blood-brain barrier discontinuity. In the case of barrier<br>discontinuity, small numbers of hypothetical signal molecules enter circulation<br>and attach to the receptor sites in the neighbouring blood vessels. The specific<br>receptors of the cells in the blood vessels stimulated by endogenous prion-like<br>molecules might initiate the repairing processes of the blood-brain barrier. In<br>prion diseases, prion molecules from external sources are similar to endogenous<br>prion-like molecules or to the hypothetical signal molecules described here.<br>Large numbers of prion molecules enter circulation and initiate repairing<br>processes in large brain areas causing the tissue damage. This damage leads to<br>new barrier discontinuities that would provoke pathological process even when the<br>exogenous prion molecules are no longer present in the circulation.<br><br>PMID: 8771048&nbsp; [PubMed \u2013 indexed for MEDLINE]<\/p>\n\n\n\n<p><strong>55. The role of gastric mast cells, enterochromaffin-like cells and parietal cells in<br>the regulation of acid secretion.<br>Kurbel S, Kurbel B.<br>Med Hypotheses. 1995 Dec;45(6):539-42.<\/strong><\/p>\n\n\n\n<p>Department of Oncology, Osijek Clinical Hospital, Croatia.<br><br>The idea presented here is that, in gastric mucosa, two independent regulatory<br>systems use the same transmitter: histamine molecules. The IgE\/mast cell system<br>is dispersed throughout the body, while the other regulates the gastric acid<br>secretion. IgE molecules in gastric mucosa are attached to the mast cells. Mast<br>cells release histamine molecules after the antigen has been recognized by IgE.<br>These molecules normally act on vascular H1 receptors to promote extravasation<br>and chemotaxy. Gastrin molecules are released from antral G cells to stimulate<br>gastric acid secretion. Their influence on parietal cells is indirectly augmented<br>by gastrin governed release of histamine molecules from enterochromaffin-like<br>cells. These histamine molecules normally act on H2 receptors of parietal cells<br>to promote gastric acid secretion. Chronic infection of gastric mucosa (i.e. with<br>Helicobacter pylori), autoimmune disorders or repetitive mucosal exposure to the<br>same antigen, can develop chronic inflammation of gastric mucosa. Gastric acid<br>secretion is diminished with secondary hypergastrinemia and increased release of<br>histamine from enterochromaffin-like cells in an attempt to stimulate the few<br>remaining parietal cells. Hypothetically, increased concentrations of released<br>histamine in gastric mucosa might activate the vascular H1 receptors with<br>extravasation and aggravated inflammation. This can further decrease the number<br>of active parietal cells, reduce gastric acid secretion and potentiate<br>hypergastrinemia. In this hypothetical setting, H1 blockers might reduce the<br>damage by abolishing the vascular reactions. The prolonged antigen load on<br>gastric mucosa can promote production of specific IgE antibodies. Further<br>exposures to the same antigen degranulate sensitized mucosal mast cells.<br>Liberated histamine can produce extravasation through the vascular H1 receptor<br>and, hypothetically, local hyperacidity through the parietal cell H2 receptors.<br>The result would be hyperacidity and hypogastrinemia with possible ulcer disease.<br>Some individuals are more predisposed to IgE production or have increased numbers<br>of mast cells that might explain why only some people develop ulcer disease after<br>H. pylori infection.<br><br>PMID: 8771047&nbsp; [PubMed \u2013 indexed for MEDLINE]<\/p>\n\n\n\n<p><strong>56. [Myelography, CT scan, electromyography and neurologic examination in the<br>diagnosis of herniated lumbar disk].<br>[Article in Croatian]<br>Kristek B, Dici\u0107 M, Vrankovi\u0107 D, Kurbel S.<br><\/strong><strong>Lijec Vjesn. 1995 May-Jun;117(5-6):133-8.<\/strong><\/p>\n\n\n\n<p>Odjel za radiodijagnostiku, Klinicka bolnica Osijek.<br><br>The research was carried out at the Clinical Hospital Osijek during a three-year<br>period. Sixty-nine patients (34 men and 35 women) with the diagnosis of lumbar<br>slipped disc who underwent surgery were followed up. The main inclusion criterion<br>was the surgical finding of hernia. The aim of the study was to obtain a clearer<br>insight into the values of the myelography and CT scan by observing a<br>sufficiently large number of patients with surgically verified hernia of lumbar<br>disc. The characteristics of neurological and EMG findings were surveyed, as<br>well. Thirty-one patients were at the age of 40-49 years and 21 were at 30-39<br>years of age. Only 5 hernias were at the level L3L4, 28 at the level L4L5, and 46<br>at the level L5S1. Sensitivity, specificity and overall accuracy of the observed<br>parameters were estimated for 41 leftwards and 30 rightwards located hernias.<br>Myelographic finding, regardless of the observed level of slipped disc, showed<br>excellent sensitivity, specificity and accuracy of diagnosis. CT finding was<br>slightly less sensitive at the level L4L5, it was 0.93, and specific at the level<br>L5S1, amounting to 0.90. Its accuracy was not substantially lower than that of<br>myelography. The pathological EMG was 0.88 sensitive, 0.83 specific and 0.84<br>accurate. The accuracy was excellent at the level L3L4, it was 0.96, but only<br>very good at the level L5S1, amounting to 0.76. A t-test of linked pairs was used<br>to compare surgical reports and diagnostic findings. There was a great similarity<br>between a CT finding and surgical one in all three levels (t-values 1.00, 0.21<br>and 0.36). Myeolography was more congruent with the surgical finding in the<br>middle level (t-values 1.65, 0.93 and 1.52). An EMG finding was significantly<br>different from that found by surgery (t-values 1.71, 1.76 and 2.71). The<br>existence of Las?gue\u2019s sign for the diagnosis of hernia was 0.93 sensitive, 0.07<br>specific (remarkably low) and 0.36 accurate. It was particularly inaccurate at<br>the level L3L4, moderately accurate at the level L4L5, and rather accurate at the<br>lowest level L5S1. The weakened Achilles tendon reflex was less sensitive than<br>Las?gue\u2019s sign, amounting to 0.80. Its specificity was 0.19 and accuracy 0.40.<br>The highest accuracy was in hernias of the lower two levels L4L5 and L5S1. The<br>existence of weakened sense was 0.91 sensitive, specificity was remarkably low,<br>amounting to 0.08, and accuracy was 0.36. It was most inaccurate at the level<br>L3L4 and slightly better at the levels L4L5 and L5S1. Disturbance of leg<br>movements showed sensitivity of only 0.60, but specificity was 0.39 and accuracy<br>0.46. It was most precise at the level L4L5. Neurological symptoms and signs were<br>insufficiently sensitive and specific for the diagnosis of lumbar disc hernia. On<br>the basis of these parameters, the level of hernia could not be exactly<br>determined.<br><br>PMID: 8600326&nbsp; [PubMed \u2013 indexed for MEDLINE]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Prof. Sven Kurbel MD, PhD \u2013 personal web pagesDept. of Physiology, Osijek Medical FacultyJ. Huttlera 4, 31000 Osijek, Croatiae-mail: sven@jware.hr 51. Simulation model of defective insulin receptors as byproducts of receptor recycling.Kurbel B, Kurbel S, Kristek Z, Jaki\u0107 M, Juri\u0107 M, Sulava D.Med Hypotheses. 1997 Aug;49(2):165-70. Department of Anaesthesiology, University Hospital Dubrava, Zagreb, Croatia. Our simulation model assumes that the defective insulin-binding receptors innon-insulin-dependent diabetes (NIDDM) patients result from functional receptorrecycling. The model is a short program written in MS&hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-94","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/kurbel.org\/index.php?rest_route=\/wp\/v2\/pages\/94","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/kurbel.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/kurbel.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/kurbel.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/kurbel.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=94"}],"version-history":[{"count":1,"href":"https:\/\/kurbel.org\/index.php?rest_route=\/wp\/v2\/pages\/94\/revisions"}],"predecessor-version":[{"id":95,"href":"https:\/\/kurbel.org\/index.php?rest_route=\/wp\/v2\/pages\/94\/revisions\/95"}],"wp:attachment":[{"href":"https:\/\/kurbel.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=94"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}