scholarly journals Advances in botulinum toxin type A for the treatment of pain

2021 ◽  
Author(s):  
Shisheng Jiang ◽  
Chaoming Huang ◽  
Yantianyu Yang ◽  
Shuhan Gao ◽  
Zihan Lin ◽  
...  

<i>Clostridium botulinum</i> (CB) is a Gram-positive anaerobic bacterium and a significant cause of food spoilage. Foodborne botulism occurs worldwide every year and even lead to death from respiratory distress in severe cases after eating botulism-contaminated food. The pathogenicity of CB lies in its ability to produce a potent neurotoxin, “botulinum toxin (BTX)”, for which eight different subtypes have already been isolated so far. Botulinum toxin type A (BTX-A) is widely used to treat critical clinical issues due to its good affinity and tolerability. Studies have shown that BTX-A injections effectively treat myofascial pain, inflammatory pain, and neuropathic pain. The current article mainly reviews the latest research progress using BTX-A in pain treatment during two years.

2002 ◽  
Vol 96 (Sup 2) ◽  
pp. A439 ◽  
Author(s):  
Michael F. Ferrante ◽  
Lisa Bearn ◽  
Robert Rothrock ◽  
Laurence King.

2005 ◽  
Vol 103 (2) ◽  
pp. 377-383 ◽  
Author(s):  
F Michael Ferrante ◽  
Lisa Bearn ◽  
Robert Rothrock ◽  
Laurence King

Background Traditional strategies for myofascial pain relief provide transient, incomplete, variable, or unpredictable outcomes. Botulinum toxin is itself an analgesic but can also cause sustained muscular relaxation, thereby possibly affording even greater relief than traditional therapies. Methods The study goal was to determine whether direct injection of botulinum toxin type A (BoNT-A) into trigger points was efficacious for cervicothoracic myofascial pain, and if so, to determine the presence or absence of a dose-response relation. One hundred thirty-two patients with cervical or shoulder myofascial pain or both and active trigger points were enrolled in a 12-week, randomized, double-blind, placebo-controlled trial. After a 2-week washout period for all medications, patients were injected with either saline or 10, 25, or 50 U BoNT-A into up to five active trigger points. The maximum doses in each experimental group were 0, 50, 125, and 250 U per patient, respectively. Patients subsequently received myofascial release physical therapy and amitriptyline, ibuprofen, and propoxyphene-acetaminophen napsylate. Follow-up visits occurred at 1, 2, 4, 6, 8, and 12 weeks. Outcome measures included visual analog pain scores, pain threshold as measured by pressure algometry, and rescue dose use of propoxyphene-acetaminophen napsylate. Results No significant differences occurred between placebo and BoNT-A groups with respect to visual analog pain scores, pressure algometry, and rescue medication. Conclusions Injection of BoNT-A directly into trigger points did not improve cervicothoracic myofascial pain. The role of direct injection of trigger points with BoNT-A is discussed in comparison to other injection methodologies in the potential genesis of pain relief.


2014 ◽  
Vol 142 (11) ◽  
pp. 2297-2301 ◽  
Author(s):  
M. A. VIRAY ◽  
J. WAMALA ◽  
R. FAGAN ◽  
C. LUQUEZ ◽  
S. MASLANKA ◽  
...  

SUMMARYBotulism has rarely been reported in Africa. In October 2008, botulism was reported in three Ugandan boarding-school students. All were hospitalized and one died. A cohort study was performed to assess food exposures among students, and clinical specimens and available food samples were tested for botulinum toxin. Three case-patients were identified; a homemade, oil-based condiment was eaten by all three. In the cohort study, no foods were significantly associated with illness. Botulinum toxin type A was confirmed in clinical samples. This is the first confirmed outbreak of foodborne botulism in Uganda. A homemade, oil-based condiment was the probable source. Consumption of homemade oil-based condiments is widespread in Ugandan schools, putting children at risk. Clinicians and public health authorities in Uganda should consider botulism when clusters of acute flaccid paralysis are seen. Additionally, schools should be warned of the hazard of homemade oil-based condiments, and take steps to prevent their use.


2021 ◽  
Vol 29 ◽  
Author(s):  
Giancarlo DE LA TORRE CANALES ◽  
Mariana Barbosa CÂMARA-SOUZA ◽  
Rodrigo Lorenzi POLUHA ◽  
Cassia Maria GRILLO ◽  
Paulo César Rodrigues CONTI ◽  
...  

Author(s):  
Jose L. de-la-Hoz ◽  
Miguel de-Pedro ◽  
Isabel Martín-Fontelles ◽  
Juan Mesa-Jimenez ◽  
Tomás Chivato ◽  
...  

2020 ◽  
Vol 27 ◽  
Author(s):  
Samuel Reyes-Long ◽  
Alfonso Alfaro-Rodríguez ◽  
Jose Luis Cortes-Altamirano ◽  
Eleazar LaraPadilla ◽  
Elizabeth Herrera-Maria ◽  
...  

Background: Botulinum toxin type A (BoNT-A) is widely employed for cosmetic purposes and in the treatment of certain diseases such as strabismus, hemifacial spasm and focal dystonia among others. BoNT-A effect mainly acts at the muscular level by inhibiting the release of acetylcholine at presynaptic levels consequently blocking the action potential in the neuromuscular junction. Despite the great progress in approval and pharmaceutical usage, improvement in displacing BoNT-A to other pathologies has remained short. Patients under diagnosis of several types of cancer experience pain in a myriad of ways; it can be experienced as hyperalgesia or allodynia, and the severity of the pain depends, in some degree, on the place that the tumor is located. Pain relief in patients diagnosed with cancer is not always optimal, and as the disease progresses, transition to more aggressive drugs, like opioids is sometimes unavoidable. In recent years BoNT-A employment in cancer has been explored, as well as an antinociceptive drug; experiments in neuropathic, inflammatory and acute pain have been carried out in animal models and humans. Although its mechanism has not been fully cleared evidence has shown that BoNT-A inhibits the secretion of pain mediators (substance P, Glutamate, and calcitonin gene related protein) from the nerve endings and dorsal root ganglion, impacting directly on the nociceptive transmission through the anterolateral and trigeminothalamic systems. Aim: Collect available literature regarding molecular, physiological and neurobiological evidence of the BoNT-A in cancer patients suffering from acute, neuropathic and inflammatory pain in order to identify possible mechanisms of action in which the BoNT-A could impact positively in pain treatment. Conclusion: BoNT-A could be an important neo-adjuvant and coadjuvant in the treatment of several types of cancer, diminish pro-tumor activity and secondary pain.


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