Chemical
Purpose: Chemical eye injury is an acute emergency that can result in vision loss. Neurotrophic keratitis (NK) is the most common long-term manifestation of chemical injury. NK due to alkali burn affects ocular surface health and is one of its most common causes. Here, we established a rabbit model...
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creator | Vohra, Mehak Gour, Abha Rajput, Jyoti Sangwan, Bha Chauhan, Monika Goel, Ka Kamath, Ajith Mathur, Umang Chandru, Arun Sangwan, Virender Singh Bhowmick, Tuhin Tiwari, Anil |
description | Purpose: Chemical eye injury is an acute emergency that can result in vision loss. Neurotrophic keratitis (NK) is the most common long-term manifestation of chemical injury. NK due to alkali burn affects ocular surface health and is one of its most common causes. Here, we established a rabbit model of corneal alkali burns to evaluate the severity of NK-associated changes. Material methods: Alkali burns were induced in NZ rabbits by treating the cornea with (i) a 5 mm circular filter paper soaked in 0.75 N NaOH for 10 s (Mild NK) and (ii) trephination using a guarded trephine (5 mm diameter and 150-micron depth), followed by alkali burn, with a 5 mm circular filter paper soaked in 0.75 N NaOH for 10 s (a severe form of NK). Immediately after, the cornea was rinsed with 10 mL of normal saline to remove traces of NaOH. Clinical features were evaluated on Day 0, Day 1, Day 7, Day 15, and Day 21 post-alkali burn using a slit lamp, Pentacam, and anterior segment optical coherence tomography (AS-OCT). NK-like changes in epithelium, sub-basal nerve plexus, and stroma were observed using in vivo confocal microscopy (IVCM), and corneal sensation were measured using an aesthesiometer post alkali injury. After 21 days, pro-inflammatory cytokines were evaluated for inflammation through ELISA. Results: Trephination followed by alkali burn resulted in the loss of epithelial layers (manifested using fluorescein stain), extensive edema, and increased corneal thickness (550 µm compared to 380 µm thickness of control) evaluated through AS-OCT and increased opacity score in alkali-treated rabbit (80 compared to 16 controls). IVCM images showed complete loss of nerve fibers, which failed to regenerate over 30 days, and loss of corneal sensation—conditions associated with NK. Cytokines evaluation of IL6, VEGF, and MMP9 indicated an increased angiogenic and pro-inflammatory milieu compared to the milder form of NK and the control. Discussion: Using clinical parameters, we demonstrated that the alkali-treated rabbit model depicts features of NK. Using IVCM in the NaOH burn animal model, we demonstrated a complete loss of nerve fibers with poor self-healing capability associated with sub-basal nerve degeneration and compromised corneal sensation. This pre-clinical rabbit model has implications for future pre-clinical research in neurotrophic keratitis. |
doi_str_mv | 10.3390/cells13050379 |
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fullrecord | <record><control><sourceid>gale</sourceid><recordid>TN_cdi_gale_infotracmisc_A786435146</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A786435146</galeid><sourcerecordid>A786435146</sourcerecordid><originalsourceid>FETCH-LOGICAL-g676-36dda9f0fb5be320b335acf0a409c52e6c8e1a516422b22e6bab31301b535ff93</originalsourceid><addsrcrecordid>eNptTkGKAjEQDOKCoh59gefRTjqdmRxl2FVB8OJdOpnEHYkKxv-zWXYPHuw6dHdRVZQQcwlLRAsrH1LKEoEAazsQYwU1VlqDHb7cIzHL-QJlGmkk0FiM2u9w7T2nqfiInHKY_e-JOH59HttttT9sdu16X51NbSo0Xcc2QnTkAipwiMQ-ApdwTyoY3wTJJI1WyqnyO3ZYWklHSDFanIjFX-yZUzj1t3h_Pthf--xP67oxGklqU1TLN6qC7rfs_RZiX_gXww8gBUZA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Chemical</title><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central Open Access</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>PubMed Central</source><creator>Vohra, Mehak ; Gour, Abha ; Rajput, Jyoti ; Sangwan, Bha ; Chauhan, Monika ; Goel, Ka ; Kamath, Ajith ; Mathur, Umang ; Chandru, Arun ; Sangwan, Virender Singh ; Bhowmick, Tuhin ; Tiwari, Anil</creator><creatorcontrib>Vohra, Mehak ; Gour, Abha ; Rajput, Jyoti ; Sangwan, Bha ; Chauhan, Monika ; Goel, Ka ; Kamath, Ajith ; Mathur, Umang ; Chandru, Arun ; Sangwan, Virender Singh ; Bhowmick, Tuhin ; Tiwari, Anil</creatorcontrib><description>Purpose: Chemical eye injury is an acute emergency that can result in vision loss. Neurotrophic keratitis (NK) is the most common long-term manifestation of chemical injury. NK due to alkali burn affects ocular surface health and is one of its most common causes. Here, we established a rabbit model of corneal alkali burns to evaluate the severity of NK-associated changes. Material methods: Alkali burns were induced in NZ rabbits by treating the cornea with (i) a 5 mm circular filter paper soaked in 0.75 N NaOH for 10 s (Mild NK) and (ii) trephination using a guarded trephine (5 mm diameter and 150-micron depth), followed by alkali burn, with a 5 mm circular filter paper soaked in 0.75 N NaOH for 10 s (a severe form of NK). Immediately after, the cornea was rinsed with 10 mL of normal saline to remove traces of NaOH. Clinical features were evaluated on Day 0, Day 1, Day 7, Day 15, and Day 21 post-alkali burn using a slit lamp, Pentacam, and anterior segment optical coherence tomography (AS-OCT). NK-like changes in epithelium, sub-basal nerve plexus, and stroma were observed using in vivo confocal microscopy (IVCM), and corneal sensation were measured using an aesthesiometer post alkali injury. After 21 days, pro-inflammatory cytokines were evaluated for inflammation through ELISA. Results: Trephination followed by alkali burn resulted in the loss of epithelial layers (manifested using fluorescein stain), extensive edema, and increased corneal thickness (550 µm compared to 380 µm thickness of control) evaluated through AS-OCT and increased opacity score in alkali-treated rabbit (80 compared to 16 controls). IVCM images showed complete loss of nerve fibers, which failed to regenerate over 30 days, and loss of corneal sensation—conditions associated with NK. Cytokines evaluation of IL6, VEGF, and MMP9 indicated an increased angiogenic and pro-inflammatory milieu compared to the milder form of NK and the control. Discussion: Using clinical parameters, we demonstrated that the alkali-treated rabbit model depicts features of NK. Using IVCM in the NaOH burn animal model, we demonstrated a complete loss of nerve fibers with poor self-healing capability associated with sub-basal nerve degeneration and compromised corneal sensation. This pre-clinical rabbit model has implications for future pre-clinical research in neurotrophic keratitis.</description><identifier>ISSN: 2073-4409</identifier><identifier>EISSN: 2073-4409</identifier><identifier>DOI: 10.3390/cells13050379</identifier><language>eng</language><publisher>MDPI AG</publisher><subject>Animal models in research ; Burns, Chemical ; Complications and side effects ; Confocal microscopy ; Degeneration ; Development and progression ; Keratitis ; Nervous system ; Physiological aspects ; Rabbits ; Translational research</subject><ispartof>Cells (Basel, Switzerland), 2024-02, Vol.13 (5)</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27924,27925</link.rule.ids></links><search><creatorcontrib>Vohra, Mehak</creatorcontrib><creatorcontrib>Gour, Abha</creatorcontrib><creatorcontrib>Rajput, Jyoti</creatorcontrib><creatorcontrib>Sangwan, Bha</creatorcontrib><creatorcontrib>Chauhan, Monika</creatorcontrib><creatorcontrib>Goel, Ka</creatorcontrib><creatorcontrib>Kamath, Ajith</creatorcontrib><creatorcontrib>Mathur, Umang</creatorcontrib><creatorcontrib>Chandru, Arun</creatorcontrib><creatorcontrib>Sangwan, Virender Singh</creatorcontrib><creatorcontrib>Bhowmick, Tuhin</creatorcontrib><creatorcontrib>Tiwari, Anil</creatorcontrib><title>Chemical</title><title>Cells (Basel, Switzerland)</title><description>Purpose: Chemical eye injury is an acute emergency that can result in vision loss. Neurotrophic keratitis (NK) is the most common long-term manifestation of chemical injury. NK due to alkali burn affects ocular surface health and is one of its most common causes. Here, we established a rabbit model of corneal alkali burns to evaluate the severity of NK-associated changes. Material methods: Alkali burns were induced in NZ rabbits by treating the cornea with (i) a 5 mm circular filter paper soaked in 0.75 N NaOH for 10 s (Mild NK) and (ii) trephination using a guarded trephine (5 mm diameter and 150-micron depth), followed by alkali burn, with a 5 mm circular filter paper soaked in 0.75 N NaOH for 10 s (a severe form of NK). Immediately after, the cornea was rinsed with 10 mL of normal saline to remove traces of NaOH. Clinical features were evaluated on Day 0, Day 1, Day 7, Day 15, and Day 21 post-alkali burn using a slit lamp, Pentacam, and anterior segment optical coherence tomography (AS-OCT). NK-like changes in epithelium, sub-basal nerve plexus, and stroma were observed using in vivo confocal microscopy (IVCM), and corneal sensation were measured using an aesthesiometer post alkali injury. After 21 days, pro-inflammatory cytokines were evaluated for inflammation through ELISA. Results: Trephination followed by alkali burn resulted in the loss of epithelial layers (manifested using fluorescein stain), extensive edema, and increased corneal thickness (550 µm compared to 380 µm thickness of control) evaluated through AS-OCT and increased opacity score in alkali-treated rabbit (80 compared to 16 controls). IVCM images showed complete loss of nerve fibers, which failed to regenerate over 30 days, and loss of corneal sensation—conditions associated with NK. Cytokines evaluation of IL6, VEGF, and MMP9 indicated an increased angiogenic and pro-inflammatory milieu compared to the milder form of NK and the control. Discussion: Using clinical parameters, we demonstrated that the alkali-treated rabbit model depicts features of NK. Using IVCM in the NaOH burn animal model, we demonstrated a complete loss of nerve fibers with poor self-healing capability associated with sub-basal nerve degeneration and compromised corneal sensation. This pre-clinical rabbit model has implications for future pre-clinical research in neurotrophic keratitis.</description><subject>Animal models in research</subject><subject>Burns, Chemical</subject><subject>Complications and side effects</subject><subject>Confocal microscopy</subject><subject>Degeneration</subject><subject>Development and progression</subject><subject>Keratitis</subject><subject>Nervous system</subject><subject>Physiological aspects</subject><subject>Rabbits</subject><subject>Translational research</subject><issn>2073-4409</issn><issn>2073-4409</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptTkGKAjEQDOKCoh59gefRTjqdmRxl2FVB8OJdOpnEHYkKxv-zWXYPHuw6dHdRVZQQcwlLRAsrH1LKEoEAazsQYwU1VlqDHb7cIzHL-QJlGmkk0FiM2u9w7T2nqfiInHKY_e-JOH59HttttT9sdu16X51NbSo0Xcc2QnTkAipwiMQ-ApdwTyoY3wTJJI1WyqnyO3ZYWklHSDFanIjFX-yZUzj1t3h_Pthf--xP67oxGklqU1TLN6qC7rfs_RZiX_gXww8gBUZA</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Vohra, Mehak</creator><creator>Gour, Abha</creator><creator>Rajput, Jyoti</creator><creator>Sangwan, Bha</creator><creator>Chauhan, Monika</creator><creator>Goel, Ka</creator><creator>Kamath, Ajith</creator><creator>Mathur, Umang</creator><creator>Chandru, Arun</creator><creator>Sangwan, Virender Singh</creator><creator>Bhowmick, Tuhin</creator><creator>Tiwari, Anil</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20240201</creationdate><title>Chemical</title><author>Vohra, Mehak ; Gour, Abha ; Rajput, Jyoti ; Sangwan, Bha ; Chauhan, Monika ; Goel, Ka ; Kamath, Ajith ; Mathur, Umang ; Chandru, Arun ; Sangwan, Virender Singh ; Bhowmick, Tuhin ; Tiwari, Anil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g676-36dda9f0fb5be320b335acf0a409c52e6c8e1a516422b22e6bab31301b535ff93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animal models in research</topic><topic>Burns, Chemical</topic><topic>Complications and side effects</topic><topic>Confocal microscopy</topic><topic>Degeneration</topic><topic>Development and progression</topic><topic>Keratitis</topic><topic>Nervous system</topic><topic>Physiological aspects</topic><topic>Rabbits</topic><topic>Translational research</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vohra, Mehak</creatorcontrib><creatorcontrib>Gour, Abha</creatorcontrib><creatorcontrib>Rajput, Jyoti</creatorcontrib><creatorcontrib>Sangwan, Bha</creatorcontrib><creatorcontrib>Chauhan, Monika</creatorcontrib><creatorcontrib>Goel, Ka</creatorcontrib><creatorcontrib>Kamath, Ajith</creatorcontrib><creatorcontrib>Mathur, Umang</creatorcontrib><creatorcontrib>Chandru, Arun</creatorcontrib><creatorcontrib>Sangwan, Virender Singh</creatorcontrib><creatorcontrib>Bhowmick, Tuhin</creatorcontrib><creatorcontrib>Tiwari, Anil</creatorcontrib><jtitle>Cells (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vohra, Mehak</au><au>Gour, Abha</au><au>Rajput, Jyoti</au><au>Sangwan, Bha</au><au>Chauhan, Monika</au><au>Goel, Ka</au><au>Kamath, Ajith</au><au>Mathur, Umang</au><au>Chandru, Arun</au><au>Sangwan, Virender Singh</au><au>Bhowmick, Tuhin</au><au>Tiwari, Anil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemical</atitle><jtitle>Cells (Basel, Switzerland)</jtitle><date>2024-02-01</date><risdate>2024</risdate><volume>13</volume><issue>5</issue><issn>2073-4409</issn><eissn>2073-4409</eissn><abstract>Purpose: Chemical eye injury is an acute emergency that can result in vision loss. Neurotrophic keratitis (NK) is the most common long-term manifestation of chemical injury. NK due to alkali burn affects ocular surface health and is one of its most common causes. Here, we established a rabbit model of corneal alkali burns to evaluate the severity of NK-associated changes. Material methods: Alkali burns were induced in NZ rabbits by treating the cornea with (i) a 5 mm circular filter paper soaked in 0.75 N NaOH for 10 s (Mild NK) and (ii) trephination using a guarded trephine (5 mm diameter and 150-micron depth), followed by alkali burn, with a 5 mm circular filter paper soaked in 0.75 N NaOH for 10 s (a severe form of NK). Immediately after, the cornea was rinsed with 10 mL of normal saline to remove traces of NaOH. Clinical features were evaluated on Day 0, Day 1, Day 7, Day 15, and Day 21 post-alkali burn using a slit lamp, Pentacam, and anterior segment optical coherence tomography (AS-OCT). NK-like changes in epithelium, sub-basal nerve plexus, and stroma were observed using in vivo confocal microscopy (IVCM), and corneal sensation were measured using an aesthesiometer post alkali injury. After 21 days, pro-inflammatory cytokines were evaluated for inflammation through ELISA. Results: Trephination followed by alkali burn resulted in the loss of epithelial layers (manifested using fluorescein stain), extensive edema, and increased corneal thickness (550 µm compared to 380 µm thickness of control) evaluated through AS-OCT and increased opacity score in alkali-treated rabbit (80 compared to 16 controls). IVCM images showed complete loss of nerve fibers, which failed to regenerate over 30 days, and loss of corneal sensation—conditions associated with NK. Cytokines evaluation of IL6, VEGF, and MMP9 indicated an increased angiogenic and pro-inflammatory milieu compared to the milder form of NK and the control. Discussion: Using clinical parameters, we demonstrated that the alkali-treated rabbit model depicts features of NK. Using IVCM in the NaOH burn animal model, we demonstrated a complete loss of nerve fibers with poor self-healing capability associated with sub-basal nerve degeneration and compromised corneal sensation. This pre-clinical rabbit model has implications for future pre-clinical research in neurotrophic keratitis.</abstract><pub>MDPI AG</pub><doi>10.3390/cells13050379</doi></addata></record> |
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subjects | Animal models in research Burns, Chemical Complications and side effects Confocal microscopy Degeneration Development and progression Keratitis Nervous system Physiological aspects Rabbits Translational research |
title | Chemical |
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