Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0920646 (renal ischemia)
 2,515 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Although the new nonionic contrast agents are safer than ionic agents, renal insufficiency and even death still occur occasionally. Therefore, we have explored the use of carbon dioxide (CO2) as an alternative angiographic contrast agent used in combination with digital subtraction angiography. Clinical observations have been made in over 800 patients. The images obtained are of equivalent diagnostic quality compared with those using conventional iodinated contrast agents. Recent advances in imaging, including "stacking," provide images comparable with iodinated contrast. Very small vessels, equivalent to third-order branches of the renal artery, can be imaged satisfactorily with CO2. Occasional studies with CO2 yield information not apparent with iodinated contrast agents, including excellent visualization of arteriovenous shunts, collateral circulations, malignant tumors, and minute amounts of arterial bleeding. Many of the advantages and disadvantages of CO2 derive from its special physical and chemical properties. The advantages include no allergic potentiation and no renal metabolism of CO2, because CO2 is cleared by the lungs and does not recirculate. Other advantages include delivery by very small catheters because of the low viscosity of CO2, minimal discomfort on injection, and very low cost. However, the low-density and compressibility of CO2 poses some special problems. Imaging requires digital subtraction angiography with electronic enhancement and injections require an experienced investigator and, ideally, a dedicated CO2 injector. The dedicated CO2 injector provides calculated, controlled dosing and rates for injection, while excluding the possibility of air contamination. The buoyancy of CO2 inhibits good filling of dependent vessels. Accordingly, CO2 does not normally produce good nephrographic images, although proximal renal arteries are normally shown clearly. Experimental studies in dogs, whose renal arteries have been injected repeatedly with very large doses of CO2, demonstrate only transient changes in renal blood flow and no endothelial cell damage. However, these studies also showed clearly that renal ischemia can occur due to a "vapor lock" phenomenon if the kidney is positioned vertically above the injection site, and recurrent injections are given without time for absorption of the arterially delivered CO2 boluses. Uncontrolled studies in over 800 patients have confirmed that CO2 likely has a very low renal toxicity. At the University of Florida, CO2 is the radiologic contrast agent of choice in patients with renal insufficiency, especially those with diabetes mellitus, and in those with pre-existing allergy to iodinated contrast agents. Further controlled clinical studies are required to define the true clinical utility and safety of CO2 compared with conventional radiologic contrast agents.
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PMID:CO2 digital angiography: a safer contrast agent for renal vascular imaging? 794 29

In this review, we analyzed the role played by central and peripheral chemoreceptors (CHRs) in vasopressin (AVP) secretion control. Central neural pathways subserving osmotic and non-osmotic control of AVP secretion are strictly correlated to brain areas participating in chemoreception mechanisms. Among the different brain areas involved in central chemoreception, the most important site has been localized in the retrotrapezoid nucleus of the rostral ventrolateral medulla. These central CHRs are able to detect very small pH/CO2 fluctuations, participating in brain blood flow regulation, acid-base balance and blood pressure control. Decreases in arterial pH and increases in arterial pCO2 stimulate AVP release by the Supraoptic and Paraventricular Nuclei. Carotid CHRs transduce low arterial O2 tension into increased action potential activity, leading to bradycardia and coronary vasodilatation via vagal stimulation, and systemic vasoconstriction via catecholaminergic stimulation. Stimulation of carotid CHRs by hypoxia increases neurohypophyseal blood flow and AVP release, an effect inhibited by CHRs denervation. Two renal CHRs have been identified: Type R1 CHRs do not have a resting discharge but are activated by renal ischemia and hypotension; Type R2 CHRs have a resting discharge and respond to backflow of urine into the renal pelvis. Signals arising from renal CHRs modulate the activity of hypothalamic AVPergic neurons: activation of R1 and R2 CHRs, following increased intrapelvic pressure with solutions of mannitol, NaCl and KCl, produces a significant increase of AVP secretion and the same effect has been obtained by the intrarenal infusion of bradykinin, which excites afferent renal nerves, as well as by the electrical stimulation of these nerves.
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PMID:Role of central and peripheral chemoreceptors in vasopressin secretion control. 2403 93