Morpho-functional disorders of the organs and systems under the control of the injured areas of the spinal cord

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В. Раскалєй
Т. Раскалєй

Abstract

One of the most important problems of modern medicine and science is the damage to the central nervous system and the solution of the problems associated with them. Injuries of the central parts of the nervous system of varying degrees of severity have post-traumatic consequences not only locally, but also in organs and systems that receive neuro-trophic control from the damaged area of the brain or spinal cord. The degree and volume and level of injury to structures such as the spinal cord cause corresponding pathological changes in controlled organs and systems, triggering a chain reaction of secondary and tertiary distant changes. They should be researched and formatted like a map of morphological, biochemical, physiological and physical changes according to the term of damage, level, volume, strength. There is a large list of various methods of researching pathological changes in the spinal cord after receiving an injury of various degrees of severity. The interest of scientists in various fields of medical science has been firmly and long-term attached to the study of the problem of spinal cord regeneration after injury. There is a large developed material, obtained thanks to many years of research. However, there are still unexplained moments of the post-traumatic pathogenesis of some pathological conditions in the body of a spinal patient, the connection of which with a spinal cord injury must be scientifically proven in order to have a full chance of solving the problem.


An interesting study was conducted in an experiment on rats with the study of soleus muscle after spinal cord injury, which proved the importance of timely establishment of a therapeutic window for the treatment of pathological changes in muscle tissue in order to prevent irreversible morphological changes. It has been proven that the ratios of various structural components of myofibrils, muscle fibers, and loose connective tissue are subject to natural changes according to the terms after spinal cord injury of the spinal cord, especially of a low level, primarily leads to morpho-functional changes in the rectum and pelvic organs. The study of not only functional problems of the rectum, but also a detailed study of the sequence of morphological changes of all structures of its wall is extremely relevant. There is progress in creating a map of biochemical changes in the contractile proteins of the smooth muscle cells of the middle lining of the rectal wall. The clinical picture is also worsened by the addition of disorders of the urinary bladder in the form of urinary incontinence, a high probability of intestinal bleeding, which in general puts the problem in the rank of social problems with a high rating in relation to the quality of life of patients. After a severe spinal cord injury, which was accompanied by a complete transection of the spinal cord with a violation of the descending autonomic pathways passing through the spinal cord, intestinal dysfunction occurs, the mechanisms of which are not yet sufficiently understood. To further understand gut dysfunction after spinal cord injury, recent preclinical studies in rodents have used anorectal manometry. Clinical and experimental studies of the manifestations and complications of a high trauma of the thoracic or cervical spine with damage to the spinal cord of the corresponding areas have proven a high probability of delayed gastric emptying, early satiety, dysphagia, constipation, urinary incontinence, nausea, abdominal distention and abdominal pain. Recent findings have shown that enteric glial cells play an important role in various neurodegenerative disorders, such as Parkinsons disease, which is characterized by motor dysfunctions caused by the progressive loss of dopaminergic neurons in the substantia nigra of the brainstem and non-motor symptoms. including gastrointestinal dysfunction.


Given the systemic impact of spinal cord injury on all physiological systems, the last few years the attention of scientists has been focused on studying the role of the gut microbiome in restoring the work of the gastrointestinal tract.


The problem of systemic dysfunctions after a spinal cord injury remains extremely relevant and still not sufficiently studied. Effective methods of their correction, according to scientists, are the use of the modeling ability of the colon microbiome, drug correction. It is promising to study the maximum possible changes in organs and systems that occur in the period after receiving a spinal cord injury, systematic data processing and creation of maps of the correspondence of spinal cord morphological, physiological, biochemical changes to changes in controlled and uncontrolled organs and systems.

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References

Lee BB, Cripps RA, Fitzharris M, Wing PC. The global map for traumatic spinal cord injury epidemiology. Spinal Cord. 2014 Feb;52(2):110-6. doi: 10.1038/sc.2012.158.

Holmes GM, Blanke EN. Gastrointestinal dysfunction after spinal cord injury. Exp Neurol. 2019 Oct;320:113009. doi: 10.1016/j.expneurol.2019.113009.

Biering-Sørensen B, Kristensen IB, Kjaer M, Biering-Sørensen F. Muscle after spinal cord injury. Muscle Nerve. 2009 Oct;40(4):499-519. doi: 10.1002/mus.21391.

Nemeth C, Banik NL, Haque A. Disruption of Neuromuscular Junction Following Spinal Cord Injury and Motor Neuron Diseases. Int J Mol Sci. 2024 Mar 20;25(6):3520. doi: 10.3390/ijms25063520. PMID: 38542497; PMCID: PMC10970763

Dos Santos ACR, Laurindo RP, Pestana FM, Heringer LDS, Canedo NHS, Martinez AMB, Marques SA. Exercise Volume Can Modulate the Regenerative Response to Spinal Cord Injury in Mice. Neurotrauma Rep. 2024 Jul 31;5(1):721-737. doi: 10.1089/neur.2024.0023.

Kok HJ, Fletcher DB, Oster JC, Conover CF, Barton ER, Yarrow JF. Transcriptomics reveals transient and dynamic muscle fibrosis and atrophy differences following spinal cord injury in rats. J Cachexia Sarcopenia Muscle. 2024 Aug;15(4):1309-1323. doi: 10.1002/jcsm.13476.

Xu X, Talifu Z, Zhang CJ, Gao F, Ke H, Pan YZ, Gong H, Du HY, Yu Y, Jing YL, Du LJ, Li JJ, Yang DG. Mechanism of skeletal muscle atrophy after spinal cord injury: A narrative review. Front Nutr. 2023 Mar 3;10:1099143. doi: 10.3389/fnut.2023.1099143. PMID: 36937344; PMCID: PMC10020380

Otzel DM, Kok HJ, Graham ZA, Barton ER, Yarrow JF. Pharmacologic approaches to prevent skeletal muscle atrophy after spinal cord injury. Curr Opin Pharmacol. 2021 Oct;60:193-199. doi: 10.1016/j.coph.2021.07.023. Epub 2021 Aug 28. PMID: 34461564; PMCID: PMC9190029.

Camilleri M. Gastrointestinal motility disorders in neurologic disease. J Clin Invest. 2021 Feb 15;131(4):e143771. doi: 10.1172/JCI143771. PMID: 33586685; PMCID: PMC7880310.

Gao T. Structural changes of rectal smooth muscle after spinal cord injury in rats. Journal of Shanghai Jiaotong University (Medical Science); (12): 963-968, 2019.

White AR, Holmes GM. Anatomical and Functional Changes to the Colonic Neuromuscular Compartment after Experimental Spinal Cord Injury. J Neurotrauma. 2018 May 1;35(9):1079-1090. doi: 10.1089/neu.2017.5369.

Frias B, Phillips AA, Squair JW, Lee AHX, Laher I, Krassioukov AV. Reduced colonic smooth muscle cholinergic responsiveness is associated with impaired bowel motility after chronic experimental high-level spinal cord injury. Auton Neurosci. 2019 Jan;216:33-38. doi: 10.1016/j.autneu.2018.08.005.

Xu P, Guo S, Xie Y, Liu Z, Liu C, Zhang X, Yang D, Gong H, Chen Y, Du L, Yu Y, Yang M. Effects of highly selective sympathectomy on neurogenic bowel dysfunction in spinal cord injury rats. Sci Rep. 2021 Aug 5;11(1):15892. doi: 10.1038/s41598-021-95158-5.

Ramp A, Holmes GM. (2019). Investigating neurogenic bowel in experimental spinal cord injury: Where to begin? Neural Regen Res. 2019 Feb;14(2):222-226. doi: 10.4103/1673-5374.244779.

Furness JB, Callaghan BP, Rivera LR, Cho HJ. The enteric nervous system and gastrointestinal innervation: integrated local and central control. Adv Exp Med Biol. 2014;817:39-71. doi: 10.1007/978-1-4939-0897-4_3.

White AR, Werner CM, Holmes GM. Diminished enteric neuromuscular transmission in the distal colon following experimental spinal cord injury. Exp Neurol. 2020 Sep;331:113377. doi: 10.1016/j.expneurol.2020.113377.

Sharkey KA, Mawe GM. The enteric nervous system. Physiol Rev. 2023 Apr 1;103(2):1487-1564. doi: 10.1152/physrev.00018.2022.

Torres RD, Rashed H, Mathur P, Castillo C, Abell T, de Paleville DGL. Autogenic biofeedback training improves autonomic responses in a participant with cervical motor complete spinal cord injury- case report. Spinal Cord Ser Cases. 2023 Jul 12;9(1):31. doi: 10.1038/s41394-023-00593-3.

Blanke EN, Ruiz-Velasco V, Holmes GM. Spinal cord injury-mediated changes in electrophysiological properties of rat gastric nodose ganglion neurons. Exp Neurol. 2022 Feb;348:113927. doi: 10.1016/j.expneurol.2021.113927.

de Jesus LB, Frota AF, de Araújo FM, Jesus RLCd, Costa MdFD, de Vasconcelos DF SA et al. Effect of the Flavonoid Rutin on the Modulation of the Myenteric Plexuses in an Experimental Model of Parkinson’s Disease. Int J Mol Sci. 2024; 25(2):1037. https://doi.org/10.3390/ijms25021037.

Sachdeva R, Hutton G, Marwaha AS, Krassioukov AV. Morphological maladaptations in sympathetic preganglionic neurons following an experimental high-thoracic spinal cord injury. Exp Neurol. 2020 May;327:113235. doi: 10.1016/j.expneurol.2020.113235.

Dieffenbach SS, Shoval HA. Treatment of postprandial hypotension with acarbose in an adult with cervical spinal cord injury: a case report. Spinal Cord Ser Cases. 2023 Dec 18;9(1):56. doi: 10.1038/s41394-023-00613-2. PMID: 38110351; PMCID: PMC10728054.

Hernandez EA, Sherman JH. Dural manipulation coinciding with transient asystole during lumbar spine surgery: illustrative case. J Neurosurg Case Lessons. 2024 Oct 28;8(18):CASE24158. doi: 10.3171/CASE24158. PMID: 39467316; PMCID: PMC11525756.

Hodgkiss DD, Williams AMM, Shackleton CS, Samejima S, Balthazaar SJT, Lam T, Krassioukov AV, Nightingale TE. Ergogenic effects of spinal cord stimulation on exercise performance following spinal cord injury. Front Neurosci. 2024 Aug 29;18:1435716. doi: 10.3389/fnins.2024.1435716. PMID: 39268039; PMCID: PMC11390595.

Lefèvre C, Le Roy C, Bessard A. Region-specific remodeling of the enteric nervous system and enteroendocrine cells in the colon of spinal cord injury patients. Sci Rep 13, 16902 (2023). https://doi.org/10.1038/s41598-023-44057-y.

Fung TC, Olson CA, Hsiao EY. Interactions between the microbiota, immune and nervous systems in health and disease. Nat Neurosci. 2017 Feb;20(2):145-155. doi: 10.1038/nn.4476.

Hamilton AM, Sampson TR. Traumatic spinal cord injury and the contributions of the post-injury microbiome. Int Rev Neurobiol. 2022;167:251-290. doi:10.1016/bs.irn.2022.06.003.

Zhang Z, Cheng N, Liang J, Deng Y, Xiang P, Hei Z, Li X. Gut microbiota changes in animal models of spinal cord injury: a preclinical systematic review and meta-analysis. Ann Med. 2023;55(2):2269379. doi: 10.1080/07853890.2023.2269379

Doelman AW, Streijger F, Majerus SJA, Damaser MS, Kwon BK. Assessing Neurogenic Lower Urinary Tract Dysfunction after Spinal Cord Injury: Animal Models in Preclinical Neuro-Urology Research. Biomedicines. 2023 May 26;11(6):1539. doi: 10.3390/biomedicines11061539.

Ferreira A, Sousa Chambel S, Avelino A, Nascimento D, Silva N, Duarte Cruz C. Urinary dysfunction after spinal cord injury: Comparing outcomes after thoracic spinal transection and contusion in the rat. Neuroscience. 2024 Oct 4;557:100-115. doi: 10.1016/j.neuroscience.2024.08.015.