Identification of arginine-vasopressin receptor 1a (Avpr1a/AVPR1A) as a novel candidate gene for chronic visceral pain
Abstract Chronic abdominal pain in the absence of ongoing disease is the hallmark of disorders of gut-brain interaction (DGBIs), including irritable bowel syndrome (IBS). While the etiology of DGBIs remains poorly understood, there is evidence that both genetic and environmental factors play a role. In this study, we report the identification and validation ofAvpr1aas a novel candidate gene for visceral hypersensitivity (VH), a primary peripheral mechanism underlying abdominal pain in DGBI/IBS. Comparing two C57BL/6 (BL/6) substrains (C57BL/6NTac and C57BL/6J) revealed differential susceptibility to the development of chronic VH following intrarectal zymosan (ZYM) instillation, a validated preclinical model for post-inflammatory IBS. Using whole genome sequencing, we identified a SNP differentiating the two strains in the 5’ intergenic region upstream ofAvpr1a, encoding the protein arginine-vasopressin receptor 1A (AVPR1A). We used behavioral, histological, and molecular approaches to identify distal colon- specific gene expression differences and neuronal hyperresponsiveness covarying withAvpr1agenotype and VH susceptibility. While the two BL/6 substrains did not differ across other gastrointestinal (GI) phenotypes (e.g., GI motility), VH-susceptible BL/6NTac mice had higher colonicAvpr1amRNA and protein expression. Moreover, neurons of the enteric nervous system were hyperresponsive to the AVPR1A agonist AVP, suggesting a role for enteric neurons in the pathology underlying VH. These results parallel our findings that patients’ colonicAvpr1amRNA expression was higher in patients with higher pain ratings. Taken together, these findings implicate differential regulation ofAvpr1aas a novel mechanism of VH-susceptibility as well as a potential therapeutic target specific to VH.Summary A combination of approaches, from genomic analysis to functional analyses, confirmAvpr1aas a high priority candidate gene for visceral pain..
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Preprint| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
bioRxiv.org - (2023) vom: 22. Dez. Zur Gesamtaufnahme - year:2023 |
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| Sprache: |
Englisch |
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| Beteiligte Personen: |
Kader, Leena [VerfasserIn] |
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| Links: |
Volltext [kostenfrei] |
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| doi: |
10.1101/2023.12.19.572390 |
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| PPN (Katalog-ID): |
XBI04194447X |
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| 245 | 1 | 0 | |a Identification of arginine-vasopressin receptor 1a (Avpr1a/AVPR1A) as a novel candidate gene for chronic visceral pain |
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| 520 | |a Abstract Chronic abdominal pain in the absence of ongoing disease is the hallmark of disorders of gut-brain interaction (DGBIs), including irritable bowel syndrome (IBS). While the etiology of DGBIs remains poorly understood, there is evidence that both genetic and environmental factors play a role. In this study, we report the identification and validation ofAvpr1aas a novel candidate gene for visceral hypersensitivity (VH), a primary peripheral mechanism underlying abdominal pain in DGBI/IBS. Comparing two C57BL/6 (BL/6) substrains (C57BL/6NTac and C57BL/6J) revealed differential susceptibility to the development of chronic VH following intrarectal zymosan (ZYM) instillation, a validated preclinical model for post-inflammatory IBS. Using whole genome sequencing, we identified a SNP differentiating the two strains in the 5’ intergenic region upstream ofAvpr1a, encoding the protein arginine-vasopressin receptor 1A (AVPR1A). We used behavioral, histological, and molecular approaches to identify distal colon- specific gene expression differences and neuronal hyperresponsiveness covarying withAvpr1agenotype and VH susceptibility. While the two BL/6 substrains did not differ across other gastrointestinal (GI) phenotypes (e.g., GI motility), VH-susceptible BL/6NTac mice had higher colonicAvpr1amRNA and protein expression. Moreover, neurons of the enteric nervous system were hyperresponsive to the AVPR1A agonist AVP, suggesting a role for enteric neurons in the pathology underlying VH. These results parallel our findings that patients’ colonicAvpr1amRNA expression was higher in patients with higher pain ratings. Taken together, these findings implicate differential regulation ofAvpr1aas a novel mechanism of VH-susceptibility as well as a potential therapeutic target specific to VH.Summary A combination of approaches, from genomic analysis to functional analyses, confirmAvpr1aas a high priority candidate gene for visceral pain. | ||
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| 650 | 4 | |a 570 |7 (dpeaa)DE-84 | |
| 700 | 1 | |a Willits, Adam |4 aut | |
| 700 | 1 | |a Meriano, Sebastian |4 aut | |
| 700 | 1 | |a Christianson, Julie A. |0 (orcid)0000-0003-4117-5192 |4 aut | |
| 700 | 1 | |a La, Jun-Ho |4 aut | |
| 700 | 1 | |a Feng, Bin |0 (orcid)0000-0001-9277-211X |4 aut | |
| 700 | 1 | |a Knight, Brittany |4 aut | |
| 700 | 1 | |a Kosova, Gulum |4 aut | |
| 700 | 1 | |a Deberry, Jennifer |4 aut | |
| 700 | 1 | |a Coates, Matthew |4 aut | |
| 700 | 1 | |a Hyams, Jeffrey |4 aut | |
| 700 | 1 | |a Baumbauer, Kyle |0 (orcid)0000-0003-0437-9209 |4 aut | |
| 700 | 1 | |a Young, Erin E. |4 aut | |
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