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Geraldine Clough

Publications and source records attributed to Geraldine Clough.

2 recordsLinked to original sources

Microdialysis--a model for studying chronic wounds.

Microdialysis has been used for more than 20 years as a method of sampling the interstitial fluid space. It has been used in both animals and human tissues, in vivo. The principle of microdialysis is based on the passive diffusion of a compound along its concentration gradient. One major advantage of this sampling technique is that it is simple, relatively cheap, and minimally invasive. Consequently, microdialysis has been employed in a variety of research and clinical settings to recover endogenous molecules and metabolites from the tissue space. It has also been used to measure the tissue penetration of xenobiotics and to follow their temporal and spatial distribution. Most recently, microdialysis has begun to be used as a diagnostic tool and its application to clinical investigation at the bedside explored. This review describes the principles of the technique of microdialysis and its current uses in both an experimental and clinical setting. It goes on to consider current methods of wound fluid sampling and the range of bioactive molecules that have been detected in wound fluid recovered using these techniques. Finally, the use of microdialysis as a novel method for sampling wound fluid in vivo and its ability to provide a fluid that is unaffected by the sampling method and that is representative of the wound environment is discussed.

Journal Article↗

The effect of the nitric oxide synthase inhibitor N-nitro-L-arginine-methyl ester on neuropeptide-induced vasodilation and protein extravasation in human skin.

Endogenous neuropeptides released from nociceptors can induce vasodilation and enhanced protein extravasation (neurogenic inflammation). The role of nitric oxide (NO) in the induction of neurogenic inflammation is controversial. In this study, dermal microdialysis was used in awake humans (n = 39) to deliver substance P (SP; 10(-7) and 10(-6)M) or calcitonin gene-related peptide (CGRP; 5 x 10(-7)M and 2 x 10(-6)M). Neuropeptide-induced local and axon reflex erythema was assessed by laser Doppler imaging. Total protein concentration in the dialysate was measured to quantify local protein extravasation. The responses were assessed in the absence and the presence of the nitric oxide synthase inhibitor, N-nitro-L-arginine-methyl ester (L-NAME) added to the perfusate at concentrations of 5, 10 or 20 mM. L-NAME (5 mM) applied via the dialysis catheters reduced local blood flow by approximately 30%. In addition, L-NAME inhibited SP-induced vasodilation by about 40% for 10(-7)M SP and 30% for 10(-6)M SP (n = 11, p < 0.01). In contrast, CGRP-induced vasodilation was only marginally inhibited by L-NAME. SP, but not CGRP, provoked a dose-dependent increase in protein extravasation. L-NAME (5 mM) inhibited this increase by up to 40% for both SP concentrations used (n = 11, p < 0.01). Higher concentrations of L-NAME did not further reduce SP- or CGRP-induced vasodilation or SP-induced protein extravasation. Exogenously applied SP induces vasodilation and protein extravasation, which is partly NO mediated, whereas CGRP-induced vasodilation appears to be NO independent.

Adult↗