Ethanol consumption as inductor of pancreatitis

Abstract

Alcohol abuse is a major cause of pancreatitis, a condition that can manifest as both acute necroinflammation and chronic damage (acinar atrophy and fibrosis). Pancreatic acinar cells can metabolize ethanol via the oxidative pathway, which generates acetaldehyde and involves the enzymes alcohol dehydrogenase and possibly cytochrome P4502E1. Additionally, ethanol can be metabolized via a nonoxidative pathway involving fatty acid ethyl ester synthases. Metabolism of ethanol by acinar and other pancreatic cells and the consequent generation of toxic metabolites, are postulated to play an important role in the development of alcohol-related acute and chronic pancreatic injury. This current work will review some recent advances in the knowledge about ethanol actions on the exocrine pancreas and its relationship to inflammatory disease and cancer.

Key Words: Pancreas; Calcium; Ethanol; Reactive oxygen species; Pancreatitis

INTRODUCTION

Pancreatitis is a potentially fatal disease in which the pancreas digests itself and its surroundings. An intracellular calcium (Ca²⁺) overload, as well as the generation of reactive oxygen species (ROS), have been indicated as the elements responsible for the initiation of the inflammatory process in the gland. One of the main causes of pancreatitis is alcohol abuse.

In the exocrine pancreas, the activation of phospholipase C (PLC)-linked receptors (R) by secretagogues produces an increase in the concentration of inositol 1,4,5-trisphosphate (IP₃) in the cytosol. IP₃ in turn releases Ca²⁺ from cytoplasmic stores, leading to an increase in cytosolic free calcium concentration ([Ca²⁺]_i)[1]. Ca²⁺ signals are not only a result of its release from intracellular stores but also a co-ordinate influx from the extracellular space[2], Ca²⁺ extrusion across the plasma membrane[3] and Ca²⁺ uptake into intracellular organelles[4].

Ca²⁺ is a universal intracellular messenger that controls a wide range of cellular processes and does so by partitioning its actions in space and time. The coordination of the movement of Ca²⁺ is used to shape Ca²⁺ signals[5]. A rise in [Ca²⁺]_i is an important early signal by which physiological secretagogues elicit the release of digestive enzymes from pancreatic acinar cells. An impairment of secretion would lead to intracellular activation of digestive enzymes which, in turn, could initiate auto-digestion of the gland and surrounding tissues and to the establishment of an inflammatory disease[6,7].

Mitogen-activated protein kinase (MAPK) family members mediate a wide variety of cellular processes in response to extracellular stimuli. Once MAPKs are activated, they phosphorylate target molecules in the cytoplasm and nucleus, resulting in the regulation of gene expression concerned with proliferation and differentiation[8]. On the other hand, Tumour Necrosis Factor (TNF) is a multifunctional proinflammatory cytokine with effects on lipid metabolism, coagulation, insulin resistance and endothelial function. Members of the TNF Receptor (TNFR) superfamily can send both survival and death signals to cells[9]. TNF family members play important roles in various physiological and pathological processes, including cell proliferation, differentiation, apoptosis and modulation of immune responses and induction of inflammation.

The exocrine pancreas can metabolize ethanol mainly via an oxidative pathway involving the enzymes alcohol dehydrogenase and cytochrome P4502E1, although a non-oxidative pathway involving fatty acid ethyl ester synthesis has been also proposed[10]. Therefore, metabolism of ethanol by pancreatic acinar cells and the consequent generation of toxic metabolites are postulated to play an important role in the development of alcohol-related pancreatic injury.

ETHANOL AND CALCIUM HOMEOSTASIS

The generation of repetitive local cytosolic Ca²⁺ signals in the apical pole of the pancreatic acinar cell is the starting point for the regulation of cellular function. Nevertheless, despite being one of the initial steps involved in cellular function, global and sustained changes in [Ca²⁺]_i that are abnormal cytosolic Ca²⁺ signals, can result in necrosis. The release of Ca²⁺ through specific channels and the inhibition of Ca²⁺ pumps in intracellular stores, followed by entry of extracellular Ca²⁺, contribute to Ca²⁺ overload[11,12]. Additionally, it has been proposed that abnormally elevated [Ca²⁺]_i is a shared phenomenon that could induce trypsin premature activation[13-15], which is a previous step that can trigger acute pancreatitis[12,16].

The actions of ethanol on Ca²⁺ homeostasis are currently under study. Its effects might be due to a direct action of ethanol on Ca²⁺ handling mechanisms or to an indirect effect, mediated by a production of ROS following ethanol metabolization or by non-oxidative metabolites of ethanol. We have shown that ethanol induces Ca²⁺ mobilization in mouse pancreatic acinar cells and that this mechanism is responsible for a ROS generation and a subsequent impairment of secretory function in this cell type[17].

A recent work shows that ethanol itself induces the release of Ca²⁺ from intracellular stores in the form of oscillations[18]. This effect was observed at doses ranging from 1 to 50 mmol/L. It has been shown that 50 mmol/L is a concentration within the range of blood alcohol levels in intoxicated humans[19]. Figure 1 shows an example of [Ca²⁺]_i oscillations evoked by ethanol. In addition, it is possible that ethanol sensitizes the tissue to physiological agonists[20]. Therefore, a transformation of physiologically evoked oscillations in [Ca²⁺]_i by agonists into a single transient signal[21] will be expected. As a consequence, ethanol leads to an increase in the total Ca²⁺ mobilization in response to the agonist[11].

Figure 1 Time-course of changes in [Ca²⁺]_i in response to ethanol. Cells were loaded with the fluorescent probe fura-2. Changes in fluorescence emitted by the fluorophore reflect changes in [Ca²⁺]_i. In this setup, pancreatic acinar cells were stimulated with 10 mmol/L ethanol, which induced an oscillatory pattern in [Ca²⁺]_i. The horizontal bar indicates the time during which ethanol was applied to the cells. (nm, nanometers).

In this sense, ethanol might present a direct action on the Ca²⁺ releasing mechanisms, whereas, on the other hand, it might be reducing the action of the pumps that extrude Ca²⁺ from the cytosol i.e. the plasma membrane Ca²⁺-ATPase (PMCA) and the sarco-endoplasmic reticulum Ca²⁺-ATPase (SERCA). A slowing down of the activity of these pumps would lead to delayed Ca²⁺ extrusion out from the cytosol and, therefore, to an accumulation of the ion within the cytosol. This inhibition of Ca²⁺ pumping activity is probably due to the generation of ROS by ethanol metabolism[11,18], as will be discussed in the following section.

On the other hand, the actions of ethanol could be directed towards the mechanisms involved in Ca²⁺ influx. Further evidences for a cytosolic Ca²⁺ overload in the presence of ethanol come from the work by Del Castillo-Vaquero et al[21], who show that Ca²⁺ entry into the cells is increased in the presence of ethanol. This effect is also due to the generation of free radicals. This increased Ca²⁺ influx into the cells might be responsible for the potentiation of [Ca²⁺]_i signals in response to physiological concentrations of cholecystokinin.

However, controversy exists and there are works that show little or no effect of ethanol on Ca²⁺ signalling. These studies propose an indirect action of ethanol on Ca²⁺ homeostasis. In this case, non-oxidative metabolites of ethanol (fatty acid ethyl esters and fatty acids) are those who evoke repetitive short-lasting [Ca²⁺]_i spikes. In addition, fatty acids elicit a marked reduction in the cytosolic adenosine triphosphate (ATP) level, pointing towards the mitochondria as the putative point of action[12,22]. More recently, it has been proposed that these metabolites of ethanol release Ca²⁺ from the thapsigargin-sensitive ER as well as from a bafilomycin-sensitive acid compartment, which is localized exclusively in the apical granular pole. The emptying of this acidic compartment is linked to intracellular activation of digestive enzymes[14].

Putting all these observations together it can be seen that the actions of ethanol on pancreatic acinar cells create a situation potentially leading to a Ca²⁺ overload, a critical process in the initiation of alcohol-related acute pancreatitis.

ETHANOL AND REACTIVE OXYGEN SPECIES

ROS are a molecular group that can be produced in the course of different physiological processes and can react with a large variety of oxidizable cellular components. Thus, ROS have been considered as pathogenic factors in a variety of tissues and cells, including the pancreas[23,24]. Now there is growing evidence indicating that the exocrine pancreas is vulnerable to damage from ROS generated by ethanol metabolism[25].

It has been proposed that ethanol induces generation of oxygen radicals in pancreatic acinar cells[11,26,27]. Indeed, ethanol leads to an increase in fluorescence of CM-H₂DCFDA, reflecting an increase in oxidation. A decrease in oxidation was observed in the absence of extracellular Ca²⁺ and in the presence of the Ca²⁺ chelator ethylene glycol-bis (2-aminoethylether)-N,N,N´,N´-tetraacetic acid (EGTA), indicating a Ca²⁺-mediated process for ethanol-evoked ROS generation. Similarly, when the cells were challenged in the presence of the intracellular Ca²⁺ chelator 1,2-Bis (2-amino-5-methylphenoxy) ethane-N,N,N´,N´-tetraacetic acid (BAPTA) and in the absence of extracellular Ca²⁺, the responses to ethanol were reduced. Thus, ethanol might exert its deleterious effects, at least in part, via generation of ROS[17]. Recently, it has been shown that oxidative metabolization of ethanol by alcohol-dehydrogenase leads to the generation of free radicals in pancreatic acinar cells[18,21]. Additionally, ethanol leads to a delayed extrusion of Ca²⁺ from the cytosol via generation of ROS[11,18]. However, the involvement of other enzymes and other metabolical routes in ethanol-derived free radicals generation cannot be excluded. Involvement of NADPH oxidase activity in ethanol-mediated ROS generation has been demonstrated. Evidence regarding this point derives from the work by Hu et al[28], who show that ethanol augments the activation of the cell’s NADPH oxidase system stimulated by platelet-derived growth factor PDGF and causes proliferation of stellate cells. Activated stellate cells are considered the principal mediators of chronic alcoholic pancreatitis/fibrosis.

Figure 2 shows the time course of changes in CM-H₂DCFDA-derived fluorescence in response to ethanol. CM-H₂DCFDA is a stable nonfluorescent molecule that passively diffuses into cells where the acetate can be cleaved by intracellular esterases to produce a polar diol that is well retained within the cells. The diol can then be oxidized by ROS to a fluorescent form. This dye has been proved to be an excellent probe for determination of ROS production[29,30].

Figure 2 Time-course of ethanol-evoked reactive oxygen species (ROS) production in mouse pancreatic acinar cells. Pancreatic acinar cells were loaded with CM-H₂DCFDA, a stable non-fluorescent molecule that yields a polar diol that is well retained within the cells. The diol can then be oxidized by ROS to a fluorescent form; therefore this dye has been proved to be an excellent probe for determination of ROS production. In this setup, stimulation of cells with 50 mmol/L ethanol (EtOH) led to a significant increase in ROS generation. At the end of the experiment H₂O₂ (100 μmol/L) was added, as a positive control for oxidation. a.u., absolute units of fluorescence.

ETHANOL AND CELLULAR PROLIFERATION

Moderate and high alcohol intake levels over a lifetime might increase cancer risk[31]. MAPK family members, including extracellular signal-regulated protein kinase (Erk), p38MAPK (p38) and c-jun NH₂-terminal kinase (JNK), mediate a wide variety of cellular processes in response to extracellular stimuli. Once MAPKs are activated, they phosphorylate target molecules in the cytoplasm and nucleus, resulting in the regulation of gene expression concerned with proliferation, migration, extracellular matrix degradation and differentiation[8]. JNK and p38MAPK family members function in a cell context-specific and cell type-specific manner to integrate signals that affect these events. Consistent with the importance of these processes in tumorigenesis, JNK and p38MAPK signalling is associated with cancer[32].

To date there are several studies that implicate MAPK pathway as a critical regulator of the effects of ethanol and its metabolite, acetaldehyde, on acinar cells. Implication of the MAPK pathway as a critical regulator of the effects of ethanol and acetaldehyde on acinar cells has been proposed[33]. Ethanol and acetaldehyde increased the activation of all 3 subfamilies (ERK 1/2, JNK and p38 kinase) of the MAPK pathway. Treatment of cells with the inhibitor SB203 580 abolished the ethanol- and acetaldehyde-induced increase in p38 MAPK activity[34]. Furthermore, ethanol- and acetaldehyde-induced activation of MAPs was blocked by the antioxidant N-acetyl-cysteine, suggesting a role of oxidative stress in the signal transduction[35].

One study suggests a potential role for these pathways in contributing to the development of alcohol-related pancreatic carcinogenesis. In this study, ethanol stimulation of cell proliferation was inhibited by inhibition of mitogen-activated protein kinase (ERK1/2) and by blocking epidermal growth factor receptor-specific tyrosine kinase[36].

On the other hand, the intracellular signalling mechanisms regulating ethanol-induced cellular activation include the MAPK pathway and the factors responsible for mediating cell activation include ethanol itself, its metabolite acetaldehyde, oxidant stress and cytokines released during episodes of alcohol-induced pancreatic necroinflammation[37].

ETHANOL AND ENZYME SECRETION

The premature activation of digestive proenzymes, specifically proteases, within the pancreatic acinar cell is an early and critical event during acute pancreatitis. One of the early events leading to alcoholic pancreatitis seems to be the effect of ethanol on stimulus-secretion coupling mechanisms. In pancreatic acinar cells, a number of PLC-acting secretagogues, such as acetylcholine and cholecystokinin, regulate secretion via activation of a number of kinases concomitantly with the generation of repetitive local cytosolic Ca²⁺ signals in the apical pole. This leads to the fusion of the secretory vesicles with the apical membrane of the acinar cell and the exocytosis of the content into the extracellular space[38].

Classically, it is known that ethanol causes a dose-dependent inhibition of enzyme synthesis without affecting exocytosis of preformed or newly synthesized protein. This is a direct inhibitory effect of ethanol and is not mediated by its metabolic processing[39]. However, treatment of pancreatic acini with ethanol does not induce any significant effect on amylase release at a wide range of concentrations (1-50 mmol/L)[17,39]. These results indicate that ethanol likely lacks a direct role in secretion although it decreases the enzymatic synthesis.

In contrast, ethanol can modulate the secretagogue-induced secretion. Incubation of cells with 50 mmol/L ethanol clearly reduces amylase release stimulated by CCK-8. The inhibitory effect of ethanol on CCK-8-induced amylase secretion was abolished by dithiothreitol, a sulfhydryl reducing agent, suggesting a ROS-mediated acton on ethanol effects[17]. The effect of ethanol in modulating the secretory response to CCK-8 could be related to the ability of ethanol to modulate the inflammatory response of the pancreas to low concentrations of CCK-8 (the molecular mechanism involved will be discussed further in the next section).

Data on the effects of ethanol on pancreatitis induced by high (supramaximal) concentration of CCK-8 are contradictory, with it being reported that alcohol can worsen[40] or produce no effect on fully developed pancreatitis[41]. However, the effect of ethanol treatment on the ability of low doses of CCK-8 to produce pancreatic damage has been clearly demonstrated[42]. The idea that ethanol sensitizes the pancreas to the action of low doses of the hormone agrees with the results of in vitro experiments. Pancreatic acinar cells isolated from rats fed ethanol for 9-12 mo were found more susceptible to cerulein-induced activation of trypsinogen and chymotrypsinogen than pancreatic acini from pair-fed control rats[42,43]. In another study, ethanol with a low dose of CCK-8 but not ethanol alone was found to generate zymogen conversion that was 6-fold higher than that caused by CCK-8 alone[44]. In summary, all these studies show that ethanol diet sensitizes rats to the development of hormone-induced pancreatitis.

ETHANOL AND INFLAMMATION

Over the past several years, evidence has been accumulating on the involvement of inflammatory cytokines and chemokines in the development of pancreatitis[20,42,45,46]. It has been reported that the levels of IL-6 and TNF-α were up-regulated in pancreas from rats with experimental pancreatitis and that the blockade of these cytokines attenuates the disease[45-49]. Furthermore, a strong correlation was observed between the IL-6 level in serum and the severity of human pancreatitis[50,51].

It has been reported that ethanol acts to sensitize the pancreas to the deleterious effects of other stimuli such as the physiological agonist CCK-8, which then leads to an inflammatory response and pancreatitis. This effect is, in part, mediated by augmenting activation of proinflammatory factors[20,42]. It has been shown that rat cerulein pancreatitis is associated with rapid NF-κB activation and that NF-κB activation mediates intrapancreatic up-regulation of IL-6[49]. Interestingly, ethanol diet potentiates the ability of CCK-8 to activate NF-κB which in turns causes an increase in the cytokine expression, suggesting that activation of NF-κB can be one of the mechanisms for ethanol-induced cytokine up-regulation in the CCK-treated animals[20,42,45].

Another observed effect of ethanol consumption is that it alone attenuated pancreatic NF-κB and decreased the expression of IL-6, iNOS and MIP-2, all of which are regulated by NF-κB[42]. Furthermore, a decrease in the levels of prostaglandin E2 has been reported and could also be involved in alcohol-induced injury in the pancreas[52]. In summary, ethanol diet causes sensitization to CCK-8-induced activation of pancreatic NF-κB and cytokine/chemokine mRNA expression, and ethanol itself causes down-regulation of NF-κB activity and mRNA levels for certain cytokines and chemokines. Both mechanisms i.e. hormone sensitization and down-regulation of NF-κB, cytokines and chemokines, could be involved in the development of the pro-inflammatory effect of ethanol in the pancreas.

CONCLUSION

Pancreatic acinar cells and other pancreatic cells can metabolize ethanol and the consequent generation of toxic metabolites are postulated to play an important role in the development of alcohol-related acute and chronic pancreatic injury. Ethanol may itself, or through its oxidative or non-oxidative metabolites, lead to Ca²⁺ mobilization from intracellular stores, sensitization of the tissue to Ca²⁺-mobilizing agonists and/or decrease the activity of Ca²⁺ transport mechanisms. As a consequence, ethanol leads to cytosolic Ca²⁺ overload. Intracellular Ca²⁺ overload has been related to ROS over production which, in turn, can further increase cytosolic Ca²⁺ accumulation because oxidants impair Ca²⁺ handling by the cell. In addition, ethanol or its metabolites inhibit secretagogue-induced secretion of enzymes, that will then accumulate within the cell. Inhibition of zymogen secretion can lead to its intracellular activation, setting the starting point for autodigestion of the gland and a consequent inflammatory process. Moreover, ethanol causes an increase in the cytokine expression in response to agonists which represents a crosstalk with inflammation pathways. On the other hand, moderate and high alcohol intake levels over a lifetime might increase cancer risk through activation of a wide variety of cellular processes in response to extracellular stimuli that can led to tumorigenesis. The putative mechanisms of action of ethanol on pancreatic acinar cells physiology are summarised in Figure 3. In conclusion, ethanol impairs the exocrine pancreas function, creating a situation potentially leading to the development of pancreatic diseases.

Figure 3 Putative mechanisms of action of ethanol on pancreatic acinar cells physiology. EtOH may, either itself or through its metabolites, sensitize the exocrine pancreas to physiological agonists. The point of action of ethanol may be at the R on the cell surface or intracellular. A stimulated Ca²⁺ release from the ER and a reduction in Ca²⁺ extrusion from the cytosol by the SERCA and/or the PMCA, will lead to accumulation of Ca²⁺ within the cytosol. This may lead to an overproduction of ROS which, in turn, will augment cytosolic Ca²⁺ accumulation, apart from other cellular effects. Cytosolic Ca²⁺ overload, together with ROS generation, may inhibit exocytosis of digestive enzymes (Z) that will accumulate inside the cell. Intracellular trapped digestive enzymes may be activated, and may initiate the autodigestion of the gland, establishing an inflammatory process. On the other hand, ethanol and/or its metabolites can activate intracellular routes for inflammation and/or cell proliferation, contributing to the impairment of cell function and to an uncontrolled cell growth. ER: Endoplasmic reticulum; SERCA: Sarco-endoplasmic reticulum Ca²⁺-ATPase; PMCA: Plasma membrane Ca²⁺-ATPase; IP₃R: Inositol 1,4,5-trisphosphate.