A new method for scoring active sweat glands.
نویسندگان
چکیده
Two different and interrelated steps are involved in the assessment of active sweat glands: stimulation of sweating and its subsequent recording and quantification. Sweat activation has been promoted by simple thermal stimulation, by intradermal injection of drugs such as methylcholine, and by dermal introduction of such drugs using iontophoresis. Gibson and Cooke’s device for iontophoresis, one of the most employed devices, provides DC current and uses large lead electrodes lined with porous material. The positive pole is dampened with 2% pilocarpine hydrochloride, and the negative one with 0.9% NaCl solution. In order to visualize sweat glands, 2 methods have been used, ie, the starch-iodine test and a method that allows permanent recording of sweat drops on silicone. The latter method consists of stimulating sweat production, drying out the skin, and then applying a thin layer of liquid silicone to it. Prior to utilization, the silicone is mixed with a catalyzer that polymerizes and solidifies the material in about 90 seconds. The solid silicone is then manually removed, and sweat drops are counted by prints left on the material. With respect to recording sweating activity, the methods reported in literature are limited to what was available in 1972, as reviewed in a study by Harris et al and reiterated in the recent Rook’s Textbook of Dermatology (2004), in which is stated “...silicone impression techniques are probably the most reliable...”. We introduce a new dynamic operational method that includes 3 devices: 1) a small battery-powered iontophoretic apparatus to stimulate sweating, 2) a digital photo or video camera to record sequential digital photographs of sweat production, and 3) a computer loaded with digital image-processing software to quantitate the sweat drop production.
منابع مشابه
Modified iodine-paper technique for the standardized determination of sweat gland activation.
Quantifying sweat gland activation provides important information when explaining differences in sweat rate between populations and physiological conditions. However, no standard technique has been proposed to measure sweat gland activation, while the reliability of sweat gland activation measurements is unknown. We examined the interrater and internal reliability of the modified-iodine paper t...
متن کاملSweat gland density and response during high-intensity exercise in athletes with spinal cord injuries
Sweat production is crucial for thermoregulation. However, sweating can be problematic for individuals with spinal cord injuries (SCI), as they display a blunting of sudomotor and vasomotor responses below the level of the injury. Sweat gland density and eccrine gland metabolism in SCI are not well understood. Consequently, this study examined sweat lactate (S-LA) (reflective of sweat gland met...
متن کاملQuantitative histochemistry of the primate skin.
Fructoaldolase activity in primate skin and appendages has been assayed with a highly sensitive fluorometric method. Epidermal fructoaldolase has characteristics similar to the fructoaldolases obtained from animal sources. The fructoaldolase activities of various skin structures are remarkably high; all glandular structures (except for apocrine sweat glands which have the highest activity of 24...
متن کاملSome observations on sweating of the Aino.
It was found by previous investigations that thermal sweat reflex was less prompt in tropic natives (3, 9) and that the total number of active sweat glands was largest in tropic natives and Japanese born in the tropics, less in Japanese immigrants to the tropics and those living in Japan proper (4) and much less in Russians settling down in North Manchuria (5). On the other hand, a lot of work ...
متن کاملFunctional requirement of aquaporin-5 in plasma membranes of sweat glands.
The distribution and function of aquaporins (AQPs) have not previously been defined in sweat glands. In this study, AQP1, AQP3, and AQP5 mRNA were demonstrated in rat paw by reverse transcription (RT)-PCR, but AQP2 and AQP4 were not. AQP1, AQP3, and AQP5 protein were confirmed in these tissues by immunoblotting. AQP1 was identified in capillary endothelial cells by immunohistochemical labeling,...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Clinics
دوره 60 6 شماره
صفحات -
تاریخ انتشار 2005