*Both authors contributed equally to this work.
Ethanol administration causes intestinal epithelial cell damage by increasing intestinal permeability and the translocation of endotoxins from intestinal bacterial flora. Heat shock proteins (HSPs) are associated with recovery and protection from cell damage. The aim of the current study was to investigate differences in the expression of HSPs in the small intestine and the biochemical changes attributable to ethanol-induced intestinal damage.
Ethanol (20%) was injected intraperitoneally (2.75 g/kg, 5.5 g/kg, 8.25 g/kg) in ICR mice and the same volume of saline was administered to controls. After 1 hour, the proximal, middle, and distal segments were taken from the small intestine and the degree of damage was analyzed. In each segment, the expression of HSPs was analyzed by western blotting. The expression of inflammatory mediators including interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), cyclooxygenase-2 (COX-2), and antioxidant enzyme such as glutathione-S-transferase were compared using real-time polymerase chain reaction assays.
In the control group, HSP70 increased in all segments of small intestine. Additionally, increases in the expression of HSP40 and HSP90 in the distal regions and an increase in HSP32 in the middle regions were observed. After ethanol treatment, greater histological damage was observed in the distal small intestine and significant decreases in HSPs were observed generally. Increased expression of IL-1β, TNF-α, and COX-2 was observed in small intestinal tissues exposed to ethanol-induced damage. However, there was no significant difference in the expression of an antioxidant enzyme.
Significant differences in the expression of HSPs in different intestinal regions were observed. These differences may have been attributable to the distribution of intestinal bacteria.
A variety of structural and functional abnormalities are caused by acute and chronic exposure to ethanol. More specifically, acute administration of ethanol damages epithelial cells of the mucosa in the small intestine, increases intestinal permeability, and induces the translocation of endotoxins. Furthermore, it also impairs active transport mechanisms and inhibits the absorption of various nutrients, including vitamins. Despite ongoing research, the exact pathological mechanisms underlying damage caused by ethanol exposure in the small intestine remain unclear.
Several reports have indicated that the structural and functional abnormalities in the small intestine following exposure to alcohol may be related to oxidative stress which was suggested as a possible mechanism for the observed ethanol-induced damage to increase intestinal permeability.
In addition to increased intestinal permeability, bacterial flora may be related to intestinal damage. Bacterial flora present in the gastric intestinal tract are present at a level of 103 colony-forming units (CFU)/mL or less in the stomach but can be increased up to 102-103 bacteria/mL, 108 bacteria/mL, and 1012 bacteria/mL in the proximal jejunum, distal ileum, and colon, respectively.
Therefore, the current study was conducted to examine pathological changes in different regions of the small intestine induced by ethanol exposure in order to investigate underlying mechanisms. Furthermore, the association between oxidative stress and small intestine damage was analyzed by assessing antioxidative levels and inflammatory factors. Lastly, changes in the expression of HSPs, which are regulatory factors for cellular oxidative damage, were also examined.
In the current study, specific-pathogen-free (SPF) 8-week-old male ICR mice were obtained from Dae Han Biolink Co. (Eumsung, Korea) and housed in specific SPF chambers at the School of Medicine in Kangwon National University. The SPF chambers in the animal room were maintained at 23±1℃ and 55±7% relative humidity and mice were acclimated for 3 days prior to the experiments. Animals had free access to water and diets and were housed on a 12:12 hour light-dark cycle. All experiments were approved by the Animal Experiment Ethics Committee of Kangwon National University in advance of the study (Approval Number: KIACUC-11-0012).
In the experiment, mice were randomly allocated into 4 groups: a control group (phosphate buffered saline [PBS] treated), and 3 ethanol groups (2.75 g/kg, 5.5 g/kg, and 8.25 g/kg). Ethanol (Merck, Damstadt, Germany) was diluted with saline (PBS) and then administered via intraperitoneal injection. Small intestines were harvested 1 hour after the injection.
ICR mice were administered either PBS (control group) or PBS diluted anhydrous ethanol (2.75 g/kg, 5.5 g/kg, or 8.25 g/kg) via intraperitoneal injection. Subsequently, alcohol-induced damage to the small intestines was analyzed. The small intestine was divided into 3 parts: the proximal jejunum, the middle of the small intestine, and the distal ileum. Each tissue segment with the size of 3 cm was collected and fixed with formalin solution and then histological changes were observed via pathological examinations using optical microscopy (Olympus BX43; Olympus Co., Tokyo, Japan).
One-hour after the intraperitoneal injection of ethanol, small intestines were harvested from ICR mice and total genomic RNA was extracted using the easy-spin Total RNA Extraction Kit (Intron, Seongnam, Korea) according to the manufacturer's instructions. Quantitative and qualitative analyses of the extracted RNA were conducted using the NanoDrop ND-1000 (NanoDrop Technologies, Wilmington, DE, USA). RNA samples were stored at -70℃ until further analysis.
The cDNA was synthesized using extracted total RNA (2 µg), 2.5 mM oligo (dt), and an Omniscript RT kit (QIAGEN, Hilden, Germany) according to the manufacturer's instructions in order to monitor changes in mRNA expression of tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and cyclooxygenase-2 (COX-2) (GeneAmp PCR system 2700; Applied Biosystems, Foster City, CA, USA). The primers for each gene were obtained from Bioneer Corp. (Daejeon, Korea) and base sequences of primers are summarized in
One-hour after the intraperitoneal injection of ethanol, small intestines were harvested from ICR mice and protein was extracted using the PRO-PREP Kit (Intron, Seongnam, Korea) per the manufacturer's instructions.
The statistical significance of the results was analyzed via the non-parametric Kruskal-Wallis test and Mann-Whitney
In the current study, the small intestines were dissected following 1 hour of ethanol administration. This was based on the results of a preliminary study which tested various time points (i.e., 30 minutes, 1 hour, 3 hours, and 5 hours) in order to determine the optimal timing for harvesting tissue. The preliminary study results showed that mice treated with high concentrations of ethanol died even before they reached several of the specific time points, which lead us to harvest tissues after 1 hour of ethanol administration, as all animals survived at least that long regardless of the ethanol dose.
Pathological analyses were conducted to explore differences among the regions of the small intestine according to the concentration of ethanol administered. Regarding damage on mucosal membranes, samples from PBS-treated mice displayed well maintained villi and normal lymphoid follicles without infiltration of inflammatory cells. In contrast, mice treated with 2.75 g/kg of ethanol showed partial falling of the villi, slight edema of the glandular layers, damage to the villi in the proximal segments and more pronounced damage to the villi in distal segments. In mice treated with 5.5 g/kg, falling of the villi was observed more frequently, as were destroyed glandular layers, erosions, and ulcers. In particular, severe erosions and ulcers were detected in distal segments where lymphoid follicles were penetrated by inflammatory cells. Mice treated with 8.25 g/kg of ethanol showed an overall loss of glandular layers, extremely severe ulcers, and damage to the serosa. Furthermore, irregular expansion of the lumen was observed, possibly due to ischemic changes in the gastrointestinal tract (
A variety of changes in the expression of HSPs were found in the small intestines in response to ethanol administration. Specifically, expression of HSP70 decreased in a dose-dependent manner. Such effects were more pronounced in the distal segments of the small intestines (
HSP40 was significantly increased in the control and low dose (2.75 g/kg) ethanol groups from the distal segment as compared to the proximal and middle segments. In contrast, HSP40 was significantly decreased in the distal segments of the small intestines from the 5.5 g/kg and 8.25 g/kg ethanol-treated groups (
Similar to HSP40, HSP90 was significantly elevated in the control group and decreased as the ethanol dosage increased in the distal segment of the small intestines (
In the control group, HSP32 was significantly increased in the middle and distal segments of the small intestines but decreased in the proximal segment by comparison. Although HSP32 was decreased in the distal segment in a dose dependent manner, its expression pattern was irregular in the proximal segment (
No difference in GST, an anti-oxidative enzyme, was noted between the control and ethanol-treated groups. Additionally, no changes were found in the different segments of the small intestines (
Acute exposure to ethanol is known to cause damage to the epithelial cells of the intestinal mucosa. Possible mechanisms underlying this phenomenon include increased intestinal permeability and the translocation of endotoxins by bacterial flora. As there are regional differences in intestinal bacteria, it is likely that structural and functional changes in the small intestines may differ from one to another region. In the current study, small intestinal damage was induced via acute administration of ethanol in order to compare various biochemical changes in the different regions and elucidate putative mechanisms underlying the damage.
Ethanol-induced damage to the small intestines has been associated with oxidative stress, which results in increased carbonylation and nitrotyrosination of cellular proteins including actin and the microtubule cytoskeleton. These changes are known to increase membrane permeability and induce the loss of integrity of tight junctions.
HSPs, molecular chaperones, are critical to cell survival and detrimental to protect cells against the harmful effects of stress-related stimuli. HSPs are synthesized in various cells when exposed not only to ethanol, but also to other environmental stressors. Although most HSPs mediate similar protective effects in response to stress, differences are apparent in their expression patterns and the biological roles depending on their class. For instance, HSP70 is known to be strongly induced by stress, whereas HSP90 is essentially expressed regardless of stress.
The results of the current study demonstrated distinct differences in damage to the small intestines of ICR mice depending on the concentration of ethanol and that damage was more pronounced in the distal region as compared to the rest of small intestines. When PBS was administered to controls, HSP40 and HSP90 were higher in the distal region while HSP70 was elevated regardless of the region examined. Conversely, HSP32 was lower in the proximal region in controls. In the ethanol-treated mice, it was difficult to find any specific correlation or site-specific associations between ethanol exposure and expression of HSPs, although differences in the expression levels of HSPs were detected and dependent on the region examined. HSP expression was significantly decreased in the distal small intestine after exposure to ethanol. HSP70 decreased in a dose-dependent manner in response to ethanol, particularly in the distal region. Similar findings were observed for HSP32, HSP40 and HSP90, however, displayed a site-specific pattern similar to that of HSP70 at a dose of 5.5 g/kg only, with different expression patterns found in the 2.75 g/kg and 8.5 g/kg ethanol-treated groups. When comparing the site-specific expression patterns of HSPs in this model, varying expression patterns and degrees of histological damage were found, in keeping with the known associations between the expression of HSPs and degrees of histological damage. In the small intestine of ICR mice, HSP70 generally showed the highest levels of expression and these levels were inversely correlated with the concentration of ethanol. It is important to note that the drastic change in HSP70 observed in distal regions was associated with severe tissue damage. In addition, the expression pattern of HSP32 was very similar to that of HSP70, suggesting that both HSPs may be critical in damage to the small intestine. However, it is difficult to elucidate the exact roles of these HSPs based on the results of the current study.
Upon the administration of ethanol, cytokines (i.e., TNF-α, and IL-1β) and inflammatory mediator (i.e., COX-2) were not showing any noticeable change among different regions of the small intestine, as found in macroscopic observations. Furthermore, no differences in the expression of GST, an anti-oxidative enzyme known to play an important role in protecting cells against oxidative stress, were detected between the control and ethanol groups, or among the regions of the small intestines in response to intestinal damage. However, it is difficult to exclude the possibility of an association between GST and intestinal damage, as the potential for differences in enzyme activity may be more significant than differences in protein expression levels. Additional studies examining putative associations between GST and intestinal damage may be warranted.
In the current study, varying magnitudes of histological damage and HSP expression in different regions of the small intestines were observed. One can expect that such site-specific changes are because we injected ethanol on lower right abdominal side. We decided to inject ethanol on the lower right side of the abdomen where there was a minimal risk of tissue damages due to a less dense distribution of blood vessels. However, the injection site itself may have influenced the results (i.e., a site specific effect of ethanol). This would seem unlikely, as HSP40 and HSP90 were exclusively increased in distal regions and HSP70 expression was elevated in a non-site-specific manner in the control group. Furthermore, HSP32 and HSP70 demonstrated similar expression patterns. Therefore, different patterns of HSP expression were likely due to their inherent features rather than the injection site. In order to provide further clarification regarding the effects of ethanol exposure on HSP expression patterns in the small intestines, a direct comparison should be made between different injection sites in future studies.
It may be possible for intestinal bacteria to impact patterns of HSP expression given the differences in distribution and classes of bacteria among regions of the small intestines. Physiological and environmental stress (e.g., microbial infection) may induce the synthesis of cellular protective HSPs on the intestinal epithelial cells. According to the results of previous studies, HSPs were modulated in response to multiple stimuli on the intestinal epithelial cells and such modulations were contingent on the exposure to intestinal probiotic bacteria.
For two different reasons, ethanol was administrated via intraperitoneal injection instead of oral exposure in the current study. First, the original goal of the study was to investigate differences among the regions of the small intestines in response to ethanol exposure. Although oral administration is the route of exposure for ethanol in humans, it may result in exposure to higher concentrations of ethanol in the proximal region compared to the distal regions and thereby make it difficult to analyze effects on the respective regions in a quantitative manner. Second, the bioavailability of ethanol in the small intestines differs due to varying degrees of gastric emptying. As such, exposure to ethanol via oral administration might be more suitable to examine chronic effects but is not recommended to determine acute effects. Therefore, ethanol was administered via intraperitoneal injection primarily to provide uniform concentrations over the small intestines in order to examine its impact on different regions. In previous studies, ethanol has been administered through intraperitoneal injection to achieve similar research objectives.
The current study had another limitation. More extensive and accurate results may have been generated if the time course of the damaging effects of ethanol on the small intestines at the concentrations of ethanol high enough to make such changes (i.e., 5.5 g/kg or higher) was monitored. However, the initial study objective was to determine damage to varying regions of the small intestines. To better understand the mechanisms underlying ethanol-induced damage, further studies regarding the time course of effects as well as the magnitudes of intestinal damage dependent on exposure time should be conducted.
Collectively, results from the current study demonstrated that the expression patterns of the HSPs assessed varied in general and also in a region-specific manner. Specifically, more pronounced histological damage was found in the distal region and HSP70 and HSP32 were decreased in particular when ethanol was administered intraperitoneally. The endotoxins produced by bacterial flora may have influenced the expression of HSPs in ethanol-induced damage to the small intestine and future studies should address this possibility.
Financial support: This study was supported by the research grant from Kangwon National University School of Medicine 2011.
Conflict of interest: None.
Pathology of the small intestinal mucosa and muscle induced by treatment with saline or ethanol (2.75 g/kg, 5.5 g/kg, 8.25 g/kg) (H&E, ×100). In saline-treated mice, villi were intact and normal lymphoid follicles were observed without infiltration of inflammatory cells. In mice treated with 2.75 g/kg of ethanol, focal falling off of villi and an edematous glandular layer were observed. These changes were more severe in the distal part with villi damage. In the group treated with 5.5 g/kg of ethanol, mulfifocal villi elimination, glandular layer destruction, erosions, and ulcers were observed with a severe aspect in the distal part. In mice treated with 8.25 g/kg of ethanol, diffuse damage extended to serosa, severe ulcers, and irregular expansion of lumen due to ischemic changes.
Comparison of the differences in expression of heat shock proteins (HSPs) in the small intestine. (A) HSP70, (B) HSP90, (C) HSP40, and (D) HSP32. The upper part of each figure shows the representative bands indicative of changes in the expression of HSPs by western blot analysis and the lower part shows a quantitatively obtained graph from the western blot analysis that was repeated 3 times. All results were obtained with 3 independent experiments and values are displayed as mean±SD. * and † indicate
Comparison of the differences in the protein expression of (A) glutathione-S-transferase (GST) and (B) mRNA expression of interleukin-1β (IL-1β), (C) tumor necrosis factor-α (TNF-α), and (D) cyclooxygenase-2 (COX-2). Figure 3A shows the representative band indicative of changes in the expression of GST by western blot analysis. Figure 3B, C, and D show results obtained by extracting mRNA via reverse transcription-PCR assay to measure the expression of each gene. All results were obtained with 3 independent experiments and values are displayed as mean±SD. * and † indicate
List of Primers Used for Real-time PCR
TNF-α, tumor necrosis factor-α; IL-1β, interleukin-1β; COX-2, cyclooxygenase-2; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.