| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-118 |
Sentence |
denotes |
Excitation and modulation of TRPA1, TRPV1, and TRPM8 channel-expressing sensory neurons by the pruritogen chloroquine. |
| T1 |
0-118 |
Sentence |
denotes |
Excitation and modulation of TRPA1, TRPV1, and TRPM8 channel-expressing sensory neurons by the pruritogen chloroquine. |
| TextSentencer_T2 |
119-189 |
Sentence |
denotes |
The sensations of pain, itch, and cold often interact with each other. |
| T2 |
119-189 |
Sentence |
denotes |
The sensations of pain, itch, and cold often interact with each other. |
| TextSentencer_T3 |
190-251 |
Sentence |
denotes |
Pain inhibits itch, whereas cold inhibits both pain and itch. |
| T3 |
190-251 |
Sentence |
denotes |
Pain inhibits itch, whereas cold inhibits both pain and itch. |
| TextSentencer_T4 |
252-332 |
Sentence |
denotes |
TRPV1 and TRPA1 channels transduce pain and itch, whereas TRPM8 transduces cold. |
| T4 |
252-332 |
Sentence |
denotes |
TRPV1 and TRPA1 channels transduce pain and itch, whereas TRPM8 transduces cold. |
| TextSentencer_T5 |
333-428 |
Sentence |
denotes |
The pruritogen chloroquine (CQ) was reported to excite TRPA1, leading to the sensation of itch. |
| T5 |
333-428 |
Sentence |
denotes |
The pruritogen chloroquine (CQ) was reported to excite TRPA1, leading to the sensation of itch. |
| TextSentencer_T6 |
429-569 |
Sentence |
denotes |
It is unclear how CQ excites and modulates TRPA1(+), TRPV1(+), and TRPM8(+) neurons and thus affects the sensations of pain, itch, and cold. |
| T6 |
429-569 |
Sentence |
denotes |
It is unclear how CQ excites and modulates TRPA1(+), TRPV1(+), and TRPM8(+) neurons and thus affects the sensations of pain, itch, and cold. |
| TextSentencer_T7 |
570-762 |
Sentence |
denotes |
Here, we show that only 43% of CQ-excited dorsal root ganglion neurons expressed TRPA1; as expected, the responses of these neurons were completely prevented by the TRPA1 antagonist HC-030031. |
| T7 |
570-762 |
Sentence |
denotes |
Here, we show that only 43% of CQ-excited dorsal root ganglion neurons expressed TRPA1; as expected, the responses of these neurons were completely prevented by the TRPA1 antagonist HC-030031. |
| TextSentencer_T8 |
763-1036 |
Sentence |
denotes |
The remaining 57% of CQ-excited neurons did not express TRPA1, and excitation was not prevented by either a TRPA1 or TRPV1 antagonist but was prevented by the general transient receptor potential canonical (TRPC) channel blocker BTP2 and the selective TRPC3 inhibitor Pyr3. |
| T8 |
763-1036 |
Sentence |
denotes |
The remaining 57% of CQ-excited neurons did not express TRPA1, and excitation was not prevented by either a TRPA1 or TRPV1 antagonist but was prevented by the general transient receptor potential canonical (TRPC) channel blocker BTP2 and the selective TRPC3 inhibitor Pyr3. |
| TextSentencer_T9 |
1037-1205 |
Sentence |
denotes |
Furthermore, CQ caused potent sensitization of TRPV1 in 51.9% of TRPV1(+) neurons and concomitant inhibition of TRPM8 in 48.8% of TRPM8(+) dorsal root ganglion neurons. |
| T9 |
1037-1205 |
Sentence |
denotes |
Furthermore, CQ caused potent sensitization of TRPV1 in 51.9% of TRPV1(+) neurons and concomitant inhibition of TRPM8 in 48.8% of TRPM8(+) dorsal root ganglion neurons. |
| TextSentencer_T10 |
1206-1343 |
Sentence |
denotes |
Sensitization of TRPV1 is caused mainly by activation of the phospholipase C-PKC pathway following activation of the CQ receptor MrgprA3. |
| T10 |
1206-1343 |
Sentence |
denotes |
Sensitization of TRPV1 is caused mainly by activation of the phospholipase C-PKC pathway following activation of the CQ receptor MrgprA3. |
| TextSentencer_T11 |
1344-1466 |
Sentence |
denotes |
By contrast, inhibition of TRPM8 is caused by a direct action of activated Gαq independent of the phospholipase C pathway. |
| T11 |
1344-1466 |
Sentence |
denotes |
By contrast, inhibition of TRPM8 is caused by a direct action of activated Gαq independent of the phospholipase C pathway. |
| TextSentencer_T12 |
1467-1575 |
Sentence |
denotes |
Our data suggest the involvement of the TRPC3 channel acting together with TRPA1 to mediate CQ-induced itch. |
| T12 |
1467-1575 |
Sentence |
denotes |
Our data suggest the involvement of the TRPC3 channel acting together with TRPA1 to mediate CQ-induced itch. |
| TextSentencer_T13 |
1576-1781 |
Sentence |
denotes |
CQ not only elicits itch by directly exciting itch-encoding neurons but also exerts previously unappreciated widespread actions on pain-, itch-, and cold-sensing neurons, leading to enhanced pain and itch. |
| T13 |
1576-1781 |
Sentence |
denotes |
CQ not only elicits itch by directly exciting itch-encoding neurons but also exerts previously unappreciated widespread actions on pain-, itch-, and cold-sensing neurons, leading to enhanced pain and itch. |