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Lesion sites

Laser ablation systems hold considerable promise if restenosis (reblocking of the arteries) rates are reduced. The rate as of 1995 is 30%, typically within six months. Mechanical or atherectomy devices to cut, shave, or pulverize plaque have been tested extensively in coronary arteries. Some of these have also been approved for peripheral use. The future of angioplasty, beyond the tremendous success of conventional balloon catheters, depends on approaches that can reduce restenosis rates. For example, if appHcation of a dmg to the lesion site turns out to be the solution to restenosis, balloon catheters would be used for both dilating the vessel and deUvering the dmg. An understanding of what happens to the arterial walls, at the cellular level, when these walls are subjected to the various types of angioplasty may need to come first. [Pg.182]

The infected area is described as painful or tender. In the case of erysipelas, the patient may complain of "burning pain" at the lesion site. [Pg.1078]

Solid fetal spinal cord tissue seeded into semipermeable mini guidance channels and implanted into a lesion site in the rat adult spinal cord... [Pg.60]

Incomplete nerve lesions provoke changes in the membrane excitability of afferents spared by the injury. These effects are the consequence of an altered cellular and signaling environment at the lesion site and in the DRG. Wallerian degeneration of axotomized nerve fibers involves degeneration and proliferation of Schwann cells, and an invasion of macrophages (discussed in Chs 30 and 36). Nerve injury is accompanied by a release of trophic... [Pg.936]

Although relatively few structural studies of the interstrand GG adduct [42, 45, 46] have been reported, the data presented reveal the structural distortion to be significantly different from that of the intrastrand adduct. The prime feature of this adduct is the cross-linking between the two strands at GC sequences, thereby causing a kink in the double helix. In this instance, however, the kink is towards the minor groove, with a value of -47° (Fig. 4.3). Another feature of this adduct not present in the other intrastrand adducts is the complementary cytosine bases extruding from the lesion site. [Pg.126]

One study has described the use of NSAID-loaded liposomes for the targeting of inflammatory lesion sites for the treatment of postoperative pain and pain related to various types of cancer [186]. In this study they showed strong and immediate analgesic effects in relieving pain with NSAID-loaded liposomes, but did not compare this with the analgesic effects of free NS AID. [Pg.112]

Based on these considerations, LCM-directed 7P-OHC delivery to the Alzheimer s lesions may inhibit amyloid toxicity via gliosis and, potentially, reduce plaque pathology. Passage of the intravenously injected LCM/7p-OHC complex across the blood-brain barrier to Alzheimer s lesion sites should be readily possible in view of the earlier-mentioned fact that scavenger receptors, both... [Pg.253]

This is a critical step and requires careful attention since it is at this stage that embolic events are most likely to develop. The risk of embolization is minimized by conservative sizing of the balloon (5 mm) and by performing a single inflation. The balloon should be deflated slowly. Mild residual stenoses (<20%) or persistence of an ulcer at the lesion site should be accepted, since aggressive stent dilatation can produce cerbral embolization. [Pg.562]

Fig. 26. A T1 time calculation image showing the prolongation of T1 at the lesion site (right kidney, arrow)... [Pg.36]

Figure 22.20. Models of two damage tolerance mechanisms. At the lesion site, template switching (the left pathway) uses the newly synthesized daughter strand as the template for DNA synthesis, thus, bypassing the lesion in an error-free manner. In contrast, translesion synthesis (the right pathway) directly copies the damaged site on the template. Consequently, mutations, shown as a square, are often generated opposite the lesion. Figure 22.20. Models of two damage tolerance mechanisms. At the lesion site, template switching (the left pathway) uses the newly synthesized daughter strand as the template for DNA synthesis, thus, bypassing the lesion in an error-free manner. In contrast, translesion synthesis (the right pathway) directly copies the damaged site on the template. Consequently, mutations, shown as a square, are often generated opposite the lesion.
Neumann S, Woolf CJ (1999) Regeiieradon of dorsal column fibers into and beyond die lesion site following adult spinal cord injury. [Pg.629]


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See also in sourсe #XX -- [ Pg.3 ]




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