Long-term BTX-A effects on bi-articular muscle: Higher passive force, limited length range of active force production and unchanged intermuscular interactions


Yilmaz E. O., KAYA C. S., AKDENİZ DOĞAN Z. D., YÜCESOY C. A.

JOURNAL OF BIOMECHANICS, cilt.126, 2021 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 126
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1016/j.jbiomech.2021.110627
  • Dergi Adı: JOURNAL OF BIOMECHANICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, Compendex, EMBASE, INSPEC, MEDLINE, SportDiscus, Veterinary Science Database
  • Anahtar Kelimeler: Botulinum toxin type A long-term effects, Bi-articular muscle, Muscle passive force, Muscle active force, Intermuscular mechanical interactions, Epimuscular myofascial force transmission, TOXIN TYPE-A, EXTRAMUSCULAR MYOFASCIAL FORCE, BOTULINUM-TOXIN, SPASTIC EQUINUS, CEREBRAL-PALSY, CHILDREN, TRANSMISSION, RAT, COMPARTMENT, NEUROTOXIN
  • Marmara Üniversitesi Adresli: Evet

Özet

Botulinum toxin type-A (BTX-A) is commonly used for spasticity management aiming at reducing joint stiffness and increasing joint range of motion in CP patients. However, previous animal studies showed acutely increased passive forces and a narrower length range of active force exertion (lrange) for muscles exposed. BTX-A can spread affecting mechanics of several muscles in a compartment, but it was shown acutely to diminish epimuscular myofascial force transmission (EMFT). Yet, our understanding of these effects in the long-term is limited and they need to be tested in a bi-articular muscle. The goal was to test the following hypotheses in a long-term rat model: exposure to BTX-A (i) has no effects on lrange and passive forces of bi-articular extensor digitorum longus (EDL) muscle and (ii) diminishes EMFT. Male Wistar rats were divided into two groups: BTX-A and control (0.1 units of BTX-A or only saline was injected into the tibialis anterior). Isometric proximal and distal EDL forces were measured simultaneously, one-month post-injection. Proximally and distally lengthening the muscle showed that BTX-A causes a significantly narrower lrange (by 14.7% distally and 32.2% proximally) and significantly increased passive muscle forces (over 2-fold both distally and proximally). Altering muscle position at constant length showed that BTX-A does not change EMFT. The findings reject both hypotheses showing that long-term exposure to BTX-A compromises bi-articular muscle's contribution to motion for both joints and the muscle's mechanical interaction with the surroundings remains unaffected. These effects which may compromise long-term spasticity management should be studied in CP patients.