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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Neuromuscular Diseases</journal-id><journal-title-group><journal-title xml:lang="en">Neuromuscular Diseases</journal-title><trans-title-group xml:lang="ru"><trans-title>Нервно-мышечные болезни</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2222-8721</issn><issn publication-format="electronic">2413-0443</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">61</article-id><article-id pub-id-type="doi">10.17650/2222-8721-2013-0-4-6-12</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LECTURES AND REVIEWS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ЛЕКЦИИ И ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Botulinum neurotoxin and chronic migraine: muscle fiber chemodenervation or nociceptic system modulation?</article-title><trans-title-group xml:lang="ru"><trans-title>Ботулинический нейротоксин и хроническая мигрень: хемоденервация мышечных волокон или модуляция ноцицептивной системы?</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Artemenko</surname><given-names>A. R.</given-names></name><name xml:lang="ru"><surname>Артеменко</surname><given-names>А. Р.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>aartemenko@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kurenkov</surname><given-names>A. L.</given-names></name><name xml:lang="ru"><surname>Куренков</surname><given-names>А. Л.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Nikitin</surname><given-names>S. S.</given-names></name><name xml:lang="ru"><surname>Никитин</surname><given-names>С. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Belomestova</surname><given-names>K. B.</given-names></name><name xml:lang="ru"><surname>Беломестова</surname><given-names>К. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">I.M. Sechenov First Moscow State Medical University</institution></aff><aff><institution xml:lang="ru">ГБОУ ВПО «Первый МГМУ им. И.М. Сеченова»</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Research Center of Child Health, Russian Academy of Medical Sciences</institution></aff><aff><institution xml:lang="ru">ФГБУ «Научный центр здоровья детей» РАМН</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Institute of General Pathology and Pathophysiology, Russian Academy of Medical Sciences, Moscow</institution></aff><aff><institution xml:lang="ru">НИИ общей патологии и патофизиологии РАМН, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2013-12-20" publication-format="electronic"><day>20</day><month>12</month><year>2013</year></pub-date><volume>3</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>6</fpage><lpage>12</lpage><history><date date-type="received" iso-8601-date="2015-02-20"><day>20</day><month>02</month><year>2015</year></date><date date-type="accepted" iso-8601-date="2015-02-20"><day>20</day><month>02</month><year>2015</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2013, Artemenko A.R., Kurenkov A.L., Nikitin S.S., Belomestova K.B.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2013, Артеменко А.Р., Куренков А.Л., Никитин С.С., Беломестова К.В.</copyright-statement><copyright-year>2013</copyright-year><copyright-holder xml:lang="en">Artemenko A.R., Kurenkov A.L., Nikitin S.S., Belomestova K.B.</copyright-holder><copyright-holder xml:lang="ru">Артеменко А.Р., Куренков А.Л., Никитин С.С., Беломестова К.В.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://nmb.abvpress.ru/jour/article/view/61">https://nmb.abvpress.ru/jour/article/view/61</self-uri><abstract xml:lang="en"><p>The results of controlled investigations suggest that botulinumtoxin type A (BTA) leads to decrease headache intensity and prevent migraine attacks. The antinociceptive mechanisms of BTA action remain unclear. Modern and previous hypothesis of antinociceptive action BTA in chronic migraine (CM) are discussed in details. Recent experimental and clinical evidence strongly suggest that BTA has aspecific antinociceptive effect realized through inhibition of proinflammatory neurotransmitters release not only from the sensory terminals but from muscle nociceptors. The mechanism of the action of BTA in CM has more than one target and is considered to involve different pathophysiological levels CM: neurogenic inflammation, peripheral and central sensitization. The administration of BTA on the PREEMPT principle (paradigm) ensures optimal neurotoxin distribution in the anatomic areas in accordance with their sensory innervation by cervical segments and sensory fibers in the trigeminal system, the terminal branches which are the major target of BTA in the treatment of CM.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>chronic migraine</kwd><kwd>botulinumtoxin type A</kwd><kwd>оnabotulinumtoxinA</kwd><kwd>chemodenervation</kwd><kwd>antinociceptive effect</kwd><kwd>antinociceptive mechanism</kwd><kwd>calcitonin gene-related peptide</kwd><kwd>neurogenic inflammation</kwd><kwd>peripheral sensitization</kwd><kwd>central sensitization</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>хроническая мигрень</kwd><kwd>ботулинический токсин типа А</kwd><kwd>оnabotulinumtoxinA</kwd><kwd>хемоденервация</kwd><kwd>антиноцицептивное действие</kwd><kwd>калицитонин-генсвязанный пептид</kwd><kwd>нейрогенное воспаление</kwd><kwd>периферическая сенситизация</kwd><kwd>центральная сенситизация</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. 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