University of Würzburg

About: University of Würzburg is a education organization based out in Wurzburg, Bayern, Germany. It is known for research contribution in the topics: Population & CAS Registry Number. The organization has 31437 authors who have published 62203 publications receiving 2337033 citations. The organization is also known as: Julius-Maximilians-Universität Würzburg & Würzburg University.

Transition-metal complexes of boron-new insights and novel coordination modes.

Abstract: Since the publication of the last review in 1998, the transition-metal chemistry of boron has continued to raise unceasing interest. Boryl complexes, representing the most extensive subclass, have remained a focus of intense research, particularly for their implication in the metal-mediated functionalization of organic substrates. Absolute novelties such as borane complexes and terminal borylene complexes have been structurally authenticated. Upon further elaboration of these compounds, the known coordination modes of boron-based ligands have grown considerably. Combined structural and theoretical investigations have contributed to elucidate the fundamental electronic characteristics of the transition-metal-boron bond and are leading to applications of these compounds. The most useful synthetic strategies for the generation of transition-metal-boron bonds are highlighted here, and the most recent and intriguing compounds that have been reported are outlined and discussed.

The Effects of Genetic Polymorphisms in the Organic Cation Transporters OCT1, OCT2, and OCT3 on the Renal Clearance of Metformin

Abstract: Organic cation transporters (OCTs) can mediate metformin transmembrane transport. We explored metformin pharmacokinetics in relation to genetic variations in OCT1, OCT2, OCT3, OCTN1, and MATE1 in 103 healthy male Caucasians. Renal clearance varied 3.8-fold and was significantly dependent on creatinine clearance (r2 = 0.42, P < 0.0001), age (r2 = 0.09, P = 0.002), and OCT1 polymorphisms. Carriers of zero, one, and two low-activity OCT1 alleles (Arg61Cys, Gly401Ser, 420del, or Gly465Arg) had mean renal clearances of 30.6, 33.1, and 37.1 l/h, respectively (P = 0.04, after adjustment for creatinine clearance and age). Immunohistochemical staining of human kidneys demonstrated OCT1 expression on the apical side of proximal and distal tubules. Increased renal clearance, in parallel with the known decreased hepatic uptake, may contribute to reduced metformin efficacy in low-activity genotypes. Renal OCT1 expression may be important not only in relation to metformin but with respect to other drugs as well.

Iodine Biokinetics and Dosimetry in Radioiodine Therapy of Thyroid Cancer: Procedures and Results of a Prospective International Controlled Study of Ablation After rhTSH or Hormone Withdrawal

Abstract: study of the effectiveness of ablation therapy with 3.7 GBq 131 I in differentiated thyroid cancer after stimulation with recombinant human TSH (rhTSH) or by thyroid hormone withdrawal (THW) are presented. Methods: Sixty-three patients were randomized after thyroidectomy to either the THW or the rhTSH group. Scintigraphic neck images were acquired starting 48 h after radioiodine administration to assess biokinetics in the thyroid remnant. The activity in blood samples was quantified and data from whole-body probe measurements and scintigraphic whole-body scans were combined to deduce retention curves in blood and whole body, respectively. The absorbed dose to the blood was calculated using a modified approach based on the formalism of the MIRD Committee of the Society of Nuclear Medicine. Results: The effective half-time in the remnant thyroid tissuewassignificantlylongerafterrhTSHthanTHW(67.6 648.8 vs. 48.0 6 52.6 h, respectively; P 5 0.01), whereas the observed differencesofthemean48-h 131 Iuptakes(0.5% 60.7%vs.0.9% 6 1.0% after THW; P 5 0.1) and residence times (0.9 6 1.3 vs. 1.4 6 1.5 h after THW; P 5 0.1) between the rhTSH and THW groups were not statistically significant. The specific absorbed dose to the blood was significantly (P ,0.0001) lower after administration of rhTSH (mean, 0.109 6 0.028 mGy/MBq; maximum, 0.18 mGy/MBq) than after THW (mean, 0.167 6 0.061 mGy/MBq; maximum, 0.35 mGy/MBq), indicating that higher activities of radioiodine might be safely administered after exogenousstimulation withrhTSH.Conclusion:Indication ofaninfluence of the residence time of radioiodine in the blood on the fractional uptake into thyroid remnant was found. A novel regimen is proposed in which therapeutic activities to be administered are determined from the individual specific blood dose.

Mechanisms of disease: Toll-like receptors in cardiovascular disease.

Abstract: The innate immune system detects highly conserved, relatively invariant structural motifs of pathogens. Toll-like receptors (TLRs) have been identified as the primary innate immune receptors. TLRs distinguish between different patterns of pathogens and activate a rapid innate immune response; however, TLRs can also be activated by host-derived molecules. In addition to being expressed in immune cells, TLRs are expressed in other tissues, such as those of the cardiovascular system. TLRs could, therefore, be a key link between cardiovascular disease development and the immune system. Indeed, evidence that TLR activation contributes to the development and progression of atherosclerosis, cardiac dysfunction in sepsis, and congestive heart failure, is convincing. Although much has been learned about TLR activation in cellular components of the cardiovascular system, the role individual TLR family members have in the pathophysiology of cardiovascular diseases and hence in clinical practice remains to be defined. Here we review the rapid progress that has been made in this field, which has improved our understanding of vascular as well as myocardial TLR function in basic and clinical science.