Intraluminal Administration of Resiniferatoxin Protects against Clostridium difficile Toxin A-Induced Colitis
Clostridium difficile toxin A is a colonic inflammatory agent that acts partially by activation of TRPV1 (transient receptor potential vanilloid type 1). Resiniferatoxin (RTX) is an excitotoxin that activates TRPV1 at low concentrations and defunctionalizes TRPV1 at high concentrations. RTX at vario...
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Online Access: | http://dx.doi.org/10.1155/2017/8438172 |
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doaj-3f5f20dbcdbe47b9a2e05a53bcf1cd182020-11-24T22:55:03ZengHindawi LimitedGastroenterology Research and Practice1687-61211687-630X2017-01-01201710.1155/2017/84381728438172Intraluminal Administration of Resiniferatoxin Protects against Clostridium difficile Toxin A-Induced ColitisSteven R. Vigna0Departments of Cell Biology and Medicine, Duke University Medical Center, Durham, NC 27710, USAClostridium difficile toxin A is a colonic inflammatory agent that acts partially by activation of TRPV1 (transient receptor potential vanilloid type 1). Resiniferatoxin (RTX) is an excitotoxin that activates TRPV1 at low concentrations and defunctionalizes TRPV1 at high concentrations. RTX at various doses was injected intraluminally into isolated ileal segments in anesthetized rats. After 3 hours, the treated segments were removed and inflammation was assessed. This acute treatment with RTX resulted in biphasic responses: (1) an increase in inflammation similar to that caused by toxin A and capsaicin at low doses of up to 100 ng RTX and (2) no inflammatory effect of RTX at higher doses (1–100 μg), consistent with a defunctionalizing or neurotoxic effect of RTX at high doses. Separately, anesthetized rats were treated with RTX enemas and one or four weeks later were challenged with toxin A. Toxin A-induced colitis was significantly inhibited one week after an RTX enema, and this effect was RTX dose dependent. When tested four weeks after administration of the RTX enema, protection against toxin A colitis was lost. In conclusion, an RTX enema protects against toxin A-induced colitis in rats for at least one week but less than four weeks.http://dx.doi.org/10.1155/2017/8438172 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Steven R. Vigna |
spellingShingle |
Steven R. Vigna Intraluminal Administration of Resiniferatoxin Protects against Clostridium difficile Toxin A-Induced Colitis Gastroenterology Research and Practice |
author_facet |
Steven R. Vigna |
author_sort |
Steven R. Vigna |
title |
Intraluminal Administration of Resiniferatoxin Protects against Clostridium difficile Toxin A-Induced Colitis |
title_short |
Intraluminal Administration of Resiniferatoxin Protects against Clostridium difficile Toxin A-Induced Colitis |
title_full |
Intraluminal Administration of Resiniferatoxin Protects against Clostridium difficile Toxin A-Induced Colitis |
title_fullStr |
Intraluminal Administration of Resiniferatoxin Protects against Clostridium difficile Toxin A-Induced Colitis |
title_full_unstemmed |
Intraluminal Administration of Resiniferatoxin Protects against Clostridium difficile Toxin A-Induced Colitis |
title_sort |
intraluminal administration of resiniferatoxin protects against clostridium difficile toxin a-induced colitis |
publisher |
Hindawi Limited |
series |
Gastroenterology Research and Practice |
issn |
1687-6121 1687-630X |
publishDate |
2017-01-01 |
description |
Clostridium difficile toxin A is a colonic inflammatory agent that acts partially by activation of TRPV1 (transient receptor potential vanilloid type 1). Resiniferatoxin (RTX) is an excitotoxin that activates TRPV1 at low concentrations and defunctionalizes TRPV1 at high concentrations. RTX at various doses was injected intraluminally into isolated ileal segments in anesthetized rats. After 3 hours, the treated segments were removed and inflammation was assessed. This acute treatment with RTX resulted in biphasic responses: (1) an increase in inflammation similar to that caused by toxin A and capsaicin at low doses of up to 100 ng RTX and (2) no inflammatory effect of RTX at higher doses (1–100 μg), consistent with a defunctionalizing or neurotoxic effect of RTX at high doses. Separately, anesthetized rats were treated with RTX enemas and one or four weeks later were challenged with toxin A. Toxin A-induced colitis was significantly inhibited one week after an RTX enema, and this effect was RTX dose dependent. When tested four weeks after administration of the RTX enema, protection against toxin A colitis was lost. In conclusion, an RTX enema protects against toxin A-induced colitis in rats for at least one week but less than four weeks. |
url |
http://dx.doi.org/10.1155/2017/8438172 |
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