期刊
JOURNAL OF CLINICAL MEDICINE
卷 10, 期 19, 页码 -出版社
MDPI
DOI: 10.3390/jcm10194609
关键词
distal diabetic sensorimotor polyneuropathy; painful and non-painful distal diabetic sensorimotor polyneuropathy; cutaneous sensory corpuscles; human glabrous skin; mechanoproteins
资金
- University of Oviedo [PAPI-20-EMERG-13]
The study found a significant decrease in the number of cutaneous mechanoreceptors in diabetic patients with distal diabetic sensorimotor polyneuropathy, especially in those experiencing pain, leading to impaired mechanosensitivity system which may partly explain the progression of the disease. Increased severity of the disease may be associated with the development of painful neuropathic symptoms, but the exact mechanism linking the absence of cutaneous mechanoreceptors to pain remains unclear.
Distal diabetic sensorimotor polyneuropathy (DDSP) is the most prevalent form of diabetic neuropathy, and some of the patients develop gradual pain. Specialized sensory structures present in the skin encode different modalities of somatosensitivity such as temperature, touch, and pain. The cutaneous sensory structures responsible for the qualities of mechanosensitivity (fine touch, vibration) are collectively known as cutaneous mechanoreceptors (Meissner corpuscles, Pacinian corpuscles, and Merkel cell-axonal complexes), which results are altered during diabetes. Here, we used immunohistochemistry to analyze the density, localization within the dermis, arrangement of corpuscular components (axons and Schwann-like cells), and expression of putative mechanoproteins (PIEZO2, ASIC2, and TRPV4) in cutaneous mechanoreceptors of subjects suffering clinically diagnosed non-painful and painful distal diabetic sensorimotor polyneuropathy. The number of Meissner corpuscles, Pacinian corpuscles, and Merkel cells was found to be severely decreased in the non-painful presentation of the disease, and almost disappeared in the painful presentation. Furthermore, there was a marked reduction in the expression of axonal and Schwann-like cell markers (with are characteristics of corpuscular denervation) as well as of all investigated mechanoproteins in the non-painful distal diabetic sensorimotor polyneuropathy, and these were absent in the painful form. Taken together, these alterations might explain, at least partly, the impairment of mechanosensitivity system associated with distal diabetic sensorimotor polyneuropathy. Furthermore, our results support that an increasing severity of DDSP may increase the risk of developing painful neuropathic symptoms. However, why the absence of cutaneous mechanoreceptors is associated with pain remains to be elucidated.
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