Rylie McDonell’s research while affiliated with University of Nebraska at Lincoln and other places

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Publications (1)


(A) Hind paw withdrawal threshold of C57Bl/6 J male mice after incision and vehicle/drug treatment. (B) Basso Motor Scale (BMS) and BMS Subscore of C57Bl/6 J male mice after incision and vehicle/drug treatment. Data represented as mean ± S.E.M and analyzed by repeated measures two-way ANOVA followed by Sidak post-hoc test (*** represents p < 0.001 ** represent p < 0.01, * represents p < 0.05 in all cases vs vehicle treatment. # represents p < 0.05 and ### represents p < 0.001 vs bupivacaine treatment, n = 8.).
(A) Hind paw withdrawal threshold of C57Bl/6 J female mice after incision and vehicle/drug treatment. (B) Basso Motor Scale (BMS) of C57Bl/6 J female mice after incision and vehicle/drug treatment. Data represented as mean ± S.E.M and analyzed by repeated measures two-way ANOVA followed by Sidak post-hoc test (*** represents p < 0.001, ** represent p < 0.01, * represents p < 0.05 in all cases vs vehicle treatment, # represents p < 0.05, n = 8.).
(A) Hind paw withdrawal threshold of C57BI/6 J male mice after incision procedure and vehicle/drug (50 μl Popliteal Block) treatment, n = 8. (B) Basso Motor Scale (BMS) of C57BI/6 J male mice after incision procedure and vehicle/drug (50 μl Popliteal Block) treatment, n = 8. Data represented as mean ± S.E.M and analyzed by repeated measures two-way ANOVA followed by Sidak post-hoc test (*** represents p < 0.001, ** represent p < 0.01, * represents p < 0.05 in all cases vs vehicle treatment, # represents p < 0.05 and ### represents p < 0.001 vs bupivacaine treatment, n = 8.).
(A). Hind paw withdrawal threshold of C57BI/6 J female mice after incision procedure and vehicle/drug (50 μl Popliteal Block) treatment, n = 7–8. (B) Basso Motor Scale (BMS) of C57BI/6 J female mice after incision procedure and vehicle/drug (50 μl Popliteal Block) treatment, n = 7–8. Data represented as mean ± S.E.M and analyzed by repeated measures two-way ANOVA followed by Sidak post-hoc test (*** represents p < 0.001, ** represent p < 0.01, * represents p < 0.05 in all cases vs vehicle treatment).
(A) The pharmacokinetics of N-001 was determined through IP injections in both male and female mice at different doses (MED and MTD) at 2,4,8,24,72 and 96 h. (B) The formation of antidrug antibodies (ADAs) was measured by ELISA. The mice were injected with N-001 at the times indicated. (C) A phalloidin potency assay was conducted for determining potential neutralization of N-001 by ADAs using SH-SY5Y cells. N-001 (2.4 pmol) was incubated with cells with a dilution series of ADA containing sera and compared to N-001 treated and untreated cells. The data are presented as means ± standard errors of the means (SEM) (error bars) from each titration performed in technical triplicates.
Preclinical characterization of the efficacy and safety of biologic N-001 as a novel pain analgesic for post-operative acute pain treatment
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July 2023

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57 Reads

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2 Citations

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Rylie McDonell

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Inhibition of actin remodeling in nerves modulates action potential propagation and therefore could be used to treat acute pain. N-001 is a novel protein analgesic engineered from several C. Botulinum toxins. N-001 targets sensory neurons through ganglioside GT1b binding and ADP-ribosylates G-actin reducing actin remodeling. The activity and efficacy of N-001 was evaluated previously in vitro and in a mouse inflammatory pain model. To assess the relevance of N-001 for treatment of acute post-surgical pain, the current study evaluated the efficacy of N-001 in a mouse hind-paw incision model by peri-incisional and popliteal nerve block administration combined with mechanical testing. N-001 provided relief of pain-like behavior over 3 days and 2 days longer than the conventional long-acting anesthetic bupivacaine. Preclinical safety studies of N-001 indicated the drug produced no toxic or adverse immunological reactions over multiple doses in mice. These results combined with past targeting results encourage further investigation of N-001 as an analgesic for post-operative pain management with the potential to function as a differential nociceptor-specific nerve block.

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Citations (1)


... A new analgesic formulation (N-001) was engineered from several C. botulinum toxins and targeting sensory neurons resulting in pain relief lasting for 3 days. Those new results encourage further studies using N-001 as a potential analgesic for post-operative pain treatment [181]. ...

Reference:

Embracing the Versatility of Botulinum Neurotoxins in Conventional and New Therapeutic Applications
Preclinical characterization of the efficacy and safety of biologic N-001 as a novel pain analgesic for post-operative acute pain treatment