Differences in Pain Biology, Perception, and Coping Strategies: Towards Sex and Gender Specific Treatments

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18 August 2020
The CB2 Agonist β-Caryophyllene in Male and Female Rats Exposed to a Model of Persistent Inflammatory Pain
Ilaria Ceccarelli
5 more and 
Anna Maria Aloisi
Formalin test 2 (FT2) in olive oil (OIL), β-caryophyllene 5 mg/kg (BCP5), and BCP 10 mg/kg (BCP10) male (left) and female (right) groups (dashed line: FT1 values for comparisons). (A,A′) Flexing duration was higher in females than in males during the I and II phases (both early and late: p < 0.007, p < 0.001, and p < 0.007, respectively). BCP5 decreased the flexing duration only in the I phase and interphase (p < 0.02 and p < 0.01, respectively), whereas BCP10 reduced it in all four phases (p < 0.02 for the I phase and p < 0.001 for the other phases). (B,B′) The licking duration was higher in females than in males only in the II phase early and late (p < 0.001 and p < 0.01, respectively). BCP5 decreased the licking duration in all phases, except the II phase early (p < 0.01, p < 0.001, and p < 0.001, respectively), whereas BCP10 reduced the licking duration in all four phases (p < 0.003 for the I phase and p < 0.001 for the other phases). (C,C′) The paw jerk frequency was higher in males than in females in the I phase (p > 0.05) and lower in BCP5 and BCP10 than in OIL in the II phase late (p < 0.001 for both). Values are the mean ± SEM.

Cannabinoids help in pain treatment through their action on CB1 and CB2 receptors. β-caryophyllene (BCP), an ancient remedy to treat pain, is a sesquiterpene found in large amounts in the essential oils of various spice and food plants such as oregano, cinnamon, and black pepper. It binds to the CB2 receptor, acting as a full agonist. Sex differences in the BCP-induced analgesic effect were studied by exposing male and female rats to a persistent/repeated painful stimulation. To simulate treatment of a repeated inflammatory condition, after the first formalin injection (FT1; 50 μl, 2.5%), rats received BCP per os for 7 days at two dosages: 5 and 10 mg/kg dissolved in olive oil (OIL). The control group was treated with OIL for 7 days. On day 8, the formalin test was repeated (FT2) with a lower formalin concentration (50 μl, 1%). During the first and second formalin tests, pain-induced responses (licking, flexing, and paw jerk) and spontaneous behaviors were recorded and analyzed. In the FT1 (before the beginning of treatment with BCP), females displayed higher pain responses than did males in terms of flexing duration during the first part of the test (I phase and interphase), while during the second part (II phase early and late) males showed higher levels than did females in licking duration. In the FT2, the pain responses generally decreased in the BCP groups in a dose-dependent manner (i.e., greater effect of BCP10), with a more pronounced reduction in males than in females; moreover, the pain responses remained high in the OIL groups and in the female BCP5 group. In conclusion, long-term intake of BCP appears to be able to decrease pain behaviors in a model of repeated inflammatory pain in both sexes, but to a greater degree in males.

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