cgrp 8 37 rat Search Results


91
Tocris rat cgrp 8 37
Primer and probe sequences used for the TaqMan real-time quantitative polymerase chain reaction analyses
Rat Cgrp 8 37, supplied by Tocris, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cgrp+8+37+rat/pmc04314689-34-5-8?v=Tocris
Average 91 stars, based on 1 article reviews
rat cgrp 8 37 - by Bioz Stars, 2026-07
91/100 stars
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93
Tocris cgrp8 37
Primer and probe sequences used for the TaqMan real-time quantitative polymerase chain reaction analyses
Cgrp8 37, supplied by Tocris, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cgrp+8+37+rat/pm30784351-83-6-7?v=Tocris
Average 93 stars, based on 1 article reviews
cgrp8 37 - by Bioz Stars, 2026-07
93/100 stars
  Buy from Supplier




Image Search Results


Primer and probe sequences used for the TaqMan real-time quantitative polymerase chain reaction analyses

Journal: Arthritis & Rheumatology (Hoboken, N.j.)

Article Title: Peripheral Calcitonin Gene-Related Peptide Receptor Activation and Mechanical Sensitization of the Joint in Rat Models of Osteoarthritis Pain

doi: 10.1002/art.38656

Figure Lengend Snippet: Primer and probe sequences used for the TaqMan real-time quantitative polymerase chain reaction analyses

Article Snippet: MIA (Sigma), rat α-CGRP (Sigma), rat CGRP 8–37 (Tocris Bioscience), and 2% Fluoro-Gold (Fluorochrome) were dissolved in sterile saline.

Techniques: Real-time Polymerase Chain Reaction, Sequencing

Calcitonin gene-related peptide (CGRP)–induced mechanical sensitization of an increased proportion of knee afferents following monosodium iodoacetate (MIA) injection. A and B, CGRP significantly increased the mechanical evoked firing rates (action potentials per second [APs/s]) of joint afferents in saline-treated (A) and MIA-treated (B) rats ( P < 0.001 by 2-way analysis of variance with Bonferroni post hoc test). Values are the mean ± SEM maximum sensitizing effects of CGRP over each 1-hour recording period (n = 9 MIA-treated rats; n = 5 saline-treated rats). C, CGRP administration reduced mechanical thresholds (minimum stimulus evoking ≥2 action potentials) in saline-treated rats to a level not significantly different from that in MIA-treated rats ( P > 0.05 for comparisons of 0.5 μg or 10 μg of CGRP versus controls, by Mann-Whitney t -test). Mechanical thresholds in MIA-treated rats were unaltered by CGRP administration. Each circle represents an individual rat (n = 7–9 MIA treated and n = 5 saline treated); horizontal lines show the median. D, The percentage of fibers sensitized by CGRP was greater in MIA-treated rats than in saline-treated rats ( P < 0.001 by Fisher's exact test). ∗ = P < 0.05; ∗∗ = P < 0.01; ∗∗∗ = P < 0.001 by Mann-Whitney t -test. vFH = von Frey hair; NS = not significant.

Journal: Arthritis & Rheumatology (Hoboken, N.j.)

Article Title: Peripheral Calcitonin Gene-Related Peptide Receptor Activation and Mechanical Sensitization of the Joint in Rat Models of Osteoarthritis Pain

doi: 10.1002/art.38656

Figure Lengend Snippet: Calcitonin gene-related peptide (CGRP)–induced mechanical sensitization of an increased proportion of knee afferents following monosodium iodoacetate (MIA) injection. A and B, CGRP significantly increased the mechanical evoked firing rates (action potentials per second [APs/s]) of joint afferents in saline-treated (A) and MIA-treated (B) rats ( P < 0.001 by 2-way analysis of variance with Bonferroni post hoc test). Values are the mean ± SEM maximum sensitizing effects of CGRP over each 1-hour recording period (n = 9 MIA-treated rats; n = 5 saline-treated rats). C, CGRP administration reduced mechanical thresholds (minimum stimulus evoking ≥2 action potentials) in saline-treated rats to a level not significantly different from that in MIA-treated rats ( P > 0.05 for comparisons of 0.5 μg or 10 μg of CGRP versus controls, by Mann-Whitney t -test). Mechanical thresholds in MIA-treated rats were unaltered by CGRP administration. Each circle represents an individual rat (n = 7–9 MIA treated and n = 5 saline treated); horizontal lines show the median. D, The percentage of fibers sensitized by CGRP was greater in MIA-treated rats than in saline-treated rats ( P < 0.001 by Fisher's exact test). ∗ = P < 0.05; ∗∗ = P < 0.01; ∗∗∗ = P < 0.001 by Mann-Whitney t -test. vFH = von Frey hair; NS = not significant.

Article Snippet: MIA (Sigma), rat α-CGRP (Sigma), rat CGRP 8–37 (Tocris Bioscience), and 2% Fluoro-Gold (Fluorochrome) were dissolved in sterile saline.

Techniques: Injection, Saline, MANN-WHITNEY

Inhibition of knee afferent mechanical evoked firing by the calcitonin gene-related peptide (CGRP) receptor antagonist CGRP 8–37 in monosodium iodoacetate (MIA)–treated rats. Representative examples of knee afferent mechanical evoked (8-, 10-, or 15-gm von Frey monofilaments) response data recorded before and after administration of 10 μg of CGRP 8–37 in a saline-treated rat (A) and an MIA-treated rat (B) are shown. The inhibitory effects of CGRP 8–37 were more pronounced following MIA treatment. Results are represented as rate histograms (1-second bins) of action potential firing of knee afferents (single units) in response to stimulation at the indicated von Frey monofilament level. Insets show an overlay of a representative fiber recording with the corresponding conduction velocity (CV; in meters/second), demonstrating single-fiber recordings; both are Aδ fibers.

Journal: Arthritis & Rheumatology (Hoboken, N.j.)

Article Title: Peripheral Calcitonin Gene-Related Peptide Receptor Activation and Mechanical Sensitization of the Joint in Rat Models of Osteoarthritis Pain

doi: 10.1002/art.38656

Figure Lengend Snippet: Inhibition of knee afferent mechanical evoked firing by the calcitonin gene-related peptide (CGRP) receptor antagonist CGRP 8–37 in monosodium iodoacetate (MIA)–treated rats. Representative examples of knee afferent mechanical evoked (8-, 10-, or 15-gm von Frey monofilaments) response data recorded before and after administration of 10 μg of CGRP 8–37 in a saline-treated rat (A) and an MIA-treated rat (B) are shown. The inhibitory effects of CGRP 8–37 were more pronounced following MIA treatment. Results are represented as rate histograms (1-second bins) of action potential firing of knee afferents (single units) in response to stimulation at the indicated von Frey monofilament level. Insets show an overlay of a representative fiber recording with the corresponding conduction velocity (CV; in meters/second), demonstrating single-fiber recordings; both are Aδ fibers.

Article Snippet: MIA (Sigma), rat α-CGRP (Sigma), rat CGRP 8–37 (Tocris Bioscience), and 2% Fluoro-Gold (Fluorochrome) were dissolved in sterile saline.

Techniques: Inhibition, Saline

Ablation of monosodium iodoacetate (MIA)–induced and medial meniscus transection (MMT)–induced mechanical sensitization of joint afferents by the calcitonin gene-related peptide (CGRP) receptor antagonist CGRP 8–37. CGRP 8–37 had no effect on mechanically evoked responses (action potentials per second [APs/s]) of joint afferents in saline-treated (A) and sham-operated (D) rats, whereas it significantly inhibited mechanically evoked responses in MIA-treated (B) and MMT-operated (E) rats ( P < 0.0001 for each comparison versus its corresponding control, by 2-way analysis of variance with Bonferroni post hoc test). Values are the mean ± SEM responses over each 1-hour recording period (n = 8 saline-treated, 6 sham-operated, 9 MIA-treated, and 8 MMT-operated rats). CGRP 8–37 had no effect on mechanical thresholds (minimum stimulus evoking ≥2 action potentials) in saline-treated (C) or sham-operated (F) rats. However, in MIA-treated (C) and MMT-operated (F) rats, thresholds in the presence of 10 μg of CGRP 8–37 were increased, reversing the osteoarthritis-induced reduction of mechanical thresholds. Each circle represents an individual rat (n = 6–9 per group); horizontal lines show the median. ∗ = P < 0.05; ∗∗ = P < 0.01; ∗∗∗ = P < 0.001, by Mann-Whitney t -test. vFH = von Frey hair.

Journal: Arthritis & Rheumatology (Hoboken, N.j.)

Article Title: Peripheral Calcitonin Gene-Related Peptide Receptor Activation and Mechanical Sensitization of the Joint in Rat Models of Osteoarthritis Pain

doi: 10.1002/art.38656

Figure Lengend Snippet: Ablation of monosodium iodoacetate (MIA)–induced and medial meniscus transection (MMT)–induced mechanical sensitization of joint afferents by the calcitonin gene-related peptide (CGRP) receptor antagonist CGRP 8–37. CGRP 8–37 had no effect on mechanically evoked responses (action potentials per second [APs/s]) of joint afferents in saline-treated (A) and sham-operated (D) rats, whereas it significantly inhibited mechanically evoked responses in MIA-treated (B) and MMT-operated (E) rats ( P < 0.0001 for each comparison versus its corresponding control, by 2-way analysis of variance with Bonferroni post hoc test). Values are the mean ± SEM responses over each 1-hour recording period (n = 8 saline-treated, 6 sham-operated, 9 MIA-treated, and 8 MMT-operated rats). CGRP 8–37 had no effect on mechanical thresholds (minimum stimulus evoking ≥2 action potentials) in saline-treated (C) or sham-operated (F) rats. However, in MIA-treated (C) and MMT-operated (F) rats, thresholds in the presence of 10 μg of CGRP 8–37 were increased, reversing the osteoarthritis-induced reduction of mechanical thresholds. Each circle represents an individual rat (n = 6–9 per group); horizontal lines show the median. ∗ = P < 0.05; ∗∗ = P < 0.01; ∗∗∗ = P < 0.001, by Mann-Whitney t -test. vFH = von Frey hair.

Article Snippet: MIA (Sigma), rat α-CGRP (Sigma), rat CGRP 8–37 (Tocris Bioscience), and 2% Fluoro-Gold (Fluorochrome) were dissolved in sterile saline.

Techniques: Saline, Comparison, Control, MANN-WHITNEY

Expression of mRNA for calcitonin gene-related peptide (CGRP) receptor components in knee joint–innervating L3–L4 dorsal root ganglia (DRGs) and modulation of the levels following treatment with monosodium iodoacetate (MIA). A, Expression of mRNA for CGRP was significantly reduced 28 days after MIA treatment. B, Calcitonin-like receptor (CLR) expression was increased 28 days after MIA treatment. C, Levels of receptor activity–modifying protein 1 (RAMP-1) were unaltered, both on day 14 and on day 28 after MIA treatment. D, Levels of mRNA for CGRP receptor component protein (CRCP) were reduced 14 days after MIA treatment. There was a small but significant increase in CRCP expression 28 days after MIA treatment. Results were normalized to β-actin expression (which was unchanged between groups and treatments). Data are shown as box plots. Each box represents the 25th to 75th percentiles (n = 6–8 rats per group). Lines inside the boxes represent the median. Lines outside the boxes represent the 10th and 90th percentiles. ∗ = P < 0.05; ∗∗ = P < 0.01 by Mann-Whitney t -test.

Journal: Arthritis & Rheumatology (Hoboken, N.j.)

Article Title: Peripheral Calcitonin Gene-Related Peptide Receptor Activation and Mechanical Sensitization of the Joint in Rat Models of Osteoarthritis Pain

doi: 10.1002/art.38656

Figure Lengend Snippet: Expression of mRNA for calcitonin gene-related peptide (CGRP) receptor components in knee joint–innervating L3–L4 dorsal root ganglia (DRGs) and modulation of the levels following treatment with monosodium iodoacetate (MIA). A, Expression of mRNA for CGRP was significantly reduced 28 days after MIA treatment. B, Calcitonin-like receptor (CLR) expression was increased 28 days after MIA treatment. C, Levels of receptor activity–modifying protein 1 (RAMP-1) were unaltered, both on day 14 and on day 28 after MIA treatment. D, Levels of mRNA for CGRP receptor component protein (CRCP) were reduced 14 days after MIA treatment. There was a small but significant increase in CRCP expression 28 days after MIA treatment. Results were normalized to β-actin expression (which was unchanged between groups and treatments). Data are shown as box plots. Each box represents the 25th to 75th percentiles (n = 6–8 rats per group). Lines inside the boxes represent the median. Lines outside the boxes represent the 10th and 90th percentiles. ∗ = P < 0.05; ∗∗ = P < 0.01 by Mann-Whitney t -test.

Article Snippet: MIA (Sigma), rat α-CGRP (Sigma), rat CGRP 8–37 (Tocris Bioscience), and 2% Fluoro-Gold (Fluorochrome) were dissolved in sterile saline.

Techniques: Expressing, Activity Assay, MANN-WHITNEY

Coexpression of the calcitonin gene-related peptide (CGRP) receptor components calcitonin-like receptor (CLR) and receptor component protein (CRCP [RCP]) by knee afferent neurons and increased CLR expression following treatment with monosodium iodoacetate (MIA). A1–A4, CLR is expressed on knee afferents (arrows) and non–knee afferent neuronal cell bodies (∗) in ipsilateral L4 dorsal root ganglia (DRGs). Slides incubated with anti–neuronal nuclei (anti-NeuN) antibodies or with Fluoro-Gold (FG) are also shown. Bar = 34 μm. B1–B4, CRCP is coexpressed with CLR on knee afferent neurons (arrows) and non–knee afferent neurons (∗). Bar = 40 μm. C, The numbers of medium (30–40 μm in diameter) and large (40–50 μm in diameter) CLR-positive knee afferents were significantly increased in MIA-treated rats. CLR-positive knee afferent cell counts were analyzed according to diameter ranges similar to those described in a previously published report . Values are the mean ± SEM of 7 rats per group. ∗ = P < 0.05 by Mann-Whitney t -test.

Journal: Arthritis & Rheumatology (Hoboken, N.j.)

Article Title: Peripheral Calcitonin Gene-Related Peptide Receptor Activation and Mechanical Sensitization of the Joint in Rat Models of Osteoarthritis Pain

doi: 10.1002/art.38656

Figure Lengend Snippet: Coexpression of the calcitonin gene-related peptide (CGRP) receptor components calcitonin-like receptor (CLR) and receptor component protein (CRCP [RCP]) by knee afferent neurons and increased CLR expression following treatment with monosodium iodoacetate (MIA). A1–A4, CLR is expressed on knee afferents (arrows) and non–knee afferent neuronal cell bodies (∗) in ipsilateral L4 dorsal root ganglia (DRGs). Slides incubated with anti–neuronal nuclei (anti-NeuN) antibodies or with Fluoro-Gold (FG) are also shown. Bar = 34 μm. B1–B4, CRCP is coexpressed with CLR on knee afferent neurons (arrows) and non–knee afferent neurons (∗). Bar = 40 μm. C, The numbers of medium (30–40 μm in diameter) and large (40–50 μm in diameter) CLR-positive knee afferents were significantly increased in MIA-treated rats. CLR-positive knee afferent cell counts were analyzed according to diameter ranges similar to those described in a previously published report . Values are the mean ± SEM of 7 rats per group. ∗ = P < 0.05 by Mann-Whitney t -test.

Article Snippet: MIA (Sigma), rat α-CGRP (Sigma), rat CGRP 8–37 (Tocris Bioscience), and 2% Fluoro-Gold (Fluorochrome) were dissolved in sterile saline.

Techniques: Expressing, Incubation, MANN-WHITNEY