Adenine nucleotide changes in the remnant liver: An early signal for regeneration after partial hepatectomy

Authors


  • Potential conflict of interest: Nothing to report.

Abstract

Liver regeneration after partial hepatectomy (PHx) is orchestrated by multiple signals from cytokines and growth factors. We investigated whether increased energy demand on the remnant liver after PHx contributes to regenerative signals. Changes in the tissue's energy state were determined from adenine nucleotide levels. Adenosine triphosphate (ATP) levels in remnant livers decreased markedly and rapidly (to 48% of control by 30 seconds post-PHx) and remained significantly lower than those in sham-operated controls for 24 to 48 hours. The ATP decrease was not reflected in corresponding increases in adenosine diphosphate (ADP) and adenosine monophosphate (AMP), resulting in a marked decline in total adenine nucleotides (TAN). We found no evidence of mitochondrial damage or uncoupling of oxidative phosphorylation. Multiple lines of evidence indicated that the decline in TAN was not caused by increased energy demand, but by ATP release from the liver. The extent of ATP loss was identical after 30% or 70% PHx, whereas fasting or hyperglycemia, conditions that greatly alter energy demand for gluconeogenesis, affected the ATP/ADP decline but not the loss of TAN. Presurgical treatment with the α-adrenergic antagonist phentolamine completely prevented loss of TAN, although changes in ATP/ADP were still apparent. Importantly, phentolamine treatment inhibited early signaling events associated with the priming stages of liver regeneration and suppressed the expression of c-fos. Pretreatment with the purinergic receptor antagonist suramin also partly suppressed early regenerative signals and c-fos expression, but without preventing TAN loss. Conclusion: The rapid loss of adenine nucleotides after PHx generates early stress signals that contribute to the onset of liver regeneration. (HEPATOLOGY 2008.)

Liver regeneration occurs in response to hepatic injury to recover lost or defective tissue in a tightly controlled process directed by a variety of cytokines and growth factor signals that has only partly been elucidated.1–3 After 70% partial hepatectomy (PHx),4 proliferation of hepatocytes occurs almost synchronously throughout the tissue, whereas differentiated liver function is maintained to meet the demands of the organism. Liver regeneration after PHx, therefore, offers a unique model of the control of cell proliferation in a differentiated system.

An early stress signal after PHx may derive from the enhanced energy demand per unit liver mass. The remnant tissue maintains liver-specific functions, such as gluconeogenesis and ureagenesis, even while adenosine triphosphate (ATP) is generated for the synthesis of proteins, nucleic acids, and other cell constituents. A 15% to 30% decline in ATP levels in the regenerating rat liver was observed throughout the first 48 hours after PHx.5–8 Likewise, a 40% to 50% drop in liver ATP was observed 24 hours after PHx in rabbits.9, 10

The remnant tissue relies on mitochondrial oxidative phosphorylation to meet energy demand. Surprisingly, defects indicative of a mitochondrial permeability transition were reported in mitochondria isolated from remnant livers after PHx.11 Diehl and coworkers12 found increased expression of uncoupling protein UCP-2 in mouse livers 3 to 6 hours after PHx, presumably as a defense against oxidative stress, which was postulated to be a signal to enhance regeneration. A decrease in respiratory coupling could contribute to declining ATP levels and impede the tissue's capacity to supply energy for biosynthesis or functional maintenance.

Whether the increased energy demand per unit liver weight itself translates into stress signals that contribute to the onset of liver regeneration has not been investigated. Liver regeneration is delayed by intravenous glucose infusion.5 These conditions would suppress gluconeogenesis and may provide an alternative ATP supply through glycolysis. Liver regeneration is defective in transgenic mice expressing mitochondrial creatine kinase in hepatocytes, an enzyme that buffers cellular ATP levels, although transfection with cytosolic creatine kinase had no such effect.13 A decline in phosphorylation potential, or other parameters related to the cellular energy state, may help signal the onset of reparative processes.

In the current study, we investigated the energy state of the remnant liver as reflected in adenine nucleotide levels with an emphasis on the earliest times (seconds to minutes) after PHx, to detect the immediate response of the tissue before the onset of adaptive coping mechanisms. This response phase has not been considered in any previous studies. A marked decline in ATP occurred almost immediately (within 15 seconds) after PHx, which was maintained throughout the prereplicative period. However, a closer investigation indicates that increased energy demand is not the major determinant of the ATP decline. Instead, a loss in total adenine nucleotides after PHx occurs in response to upstream stress signals. Importantly, conditions that prevented the loss of adenine nucleotides or that inhibited purinergic receptor activation suppressed regenerative signaling responses and expression of immediate-early gene expression associated with the priming phase. We conclude that the rapid changes in energy state of the liver after PHx contribute to early signaling events associated with the onset of liver regeneration.

Abbreviations

ADP, adenosine diphosphate; AMP, adenosine monophosphate; AMPK, adenosine monophosphate kinase; ATP, adenosine triphosphate; BHB/AcAc, β-hydroxybutyrate/acetoacetate; gww, gram net weight; JNK, Jun N-terminal kinase; L/P, lactate/pyruvate; NAD, nicotinamide adenine dinucleotide; NAD+, oxidized form of NAD; NADH, reduced form of NAD; PHx, partial hepatectomy; TAN, total adenine nucleotides.

Materials and Methods

Materials.

Biochemicals and enzymes were purchased from Sigma (St. Louis, MO) or Roche (Indianapolis, IN). Antibodies were obtained from Cell Signaling Technology (Danvers, MA) and Upstate Biotechnology (Lake Placid, NY). All other reagents were analytical grade.

Animal Protocols.

Male Sprague-Dawley rats (300-400 g) were subjected to 70% (medial and left lateral lobes) or 30% (left lateral lobe only) PHx4 under isoflurane anesthesia and allowed to recover for various periods. For sham surgeries, livers were externalized and gently palpated to mimic the surgical stress of the PHx procedure. For regeneration times of 15 minutes or less, animals were kept under anesthesia, and external tissue layers were covered with gauze (up to 5 minutes) or loosely sutured (for 15 minutes). Survival rates for PHx and sham surgeries was 100%. The time of ligation of the liver lobes before excision was the zero time point for PHx. Livers were freeze-clamped within 4 seconds of excision using aluminum clamps precooled in liquid nitrogen.14 Frozen tissue wafers (thickness < 0.5 mm, weight 2-3 g) were stored at −80°C. Parallel PHx and sham livers were processed for all time points, except very early times (<1 min). Externalization and palpation of the liver for sham surgeries was used as the zero-time for sham surgeries. However, this does not provide a precise zero time point compatible with freeze-clamping within 15 to 30 seconds similar to the PHx procedure. Liver samples from anesthetized animals freeze-clamped within 10 seconds of opening the abdomen served as controls for 15-second to 30-second regenerating livers.

Tissue Processing.

For metabolite assays, freeze-clamped liver was processed by the method of Williamson et al.14 Liver samples (500-800 mg) were crushed and homogenized in 10 volumes of cold 20% (wt/vol) HClO4. Supernatants were neutralized with ice-cold KOH, centrifuged at 4°C (20 minutes, 24,000g) to remove KClO4, and stored at −80°C for adenine nucleotide analysis. For other metabolite assays, neutralized extracts were treated with 60 to 80 mesh Florisil (0.1 g/mL) and centrifuged (10 minutes, 7800g, 4°C) to reduce nonspecific reduced nicotinamide adenine dinucleotide (NADH) oxidation.14

For protein analysis, freeze-clamped tissue was homogenized in lysis buffer containing 50 mM 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid (HEPES) (pH 7.4), 150 mM NaCl, 5 mM ethylene glycol tetra-acetic acid, 10% glycerol, 1% Triton X-100, 150 mM NaF, 10 mM Na pyrophosphate, 1 mM Na ortho-vanadate, and complete protease inhibitor cocktail (Roche Diagnostics, Basel, Switzerland).

Liver mitochondria were isolated by differential centrifugation, suspended in 0.25 M sucrose, 5 mM HEPES (pH 7.3), and incubated exactly as described previously.15 State 3 and state 4 respiration rates were measured with glutamate (+ malate) or succinate (+ Amytal) as substrates.

Assays.

Metabolites were assayed spectrophotometrically by enzymatic analysis.16 Recoveries were 95% to 105%. Blood glucose was measured with a MediSense Precision QID glucometer (Abbott Laboratories Inc., Bedford, MA). Signaling proteins were analyzed by western blotting after separation by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-Page) on 4% to 12% Bis-Tris NuPAGE gradient gels (Invitrogen).

Gene expression was measured by quantitative reverse transcription polymerase chain reaction. Total RNA was isolated using TRIzol reagent (Invitrogen, Carlsbad, CA) according to the manufacturer's instructions. Complementary DNA templates were synthesized using SuperScript II reverse transcriptase and oligo(dT) primer (Invitrogen). Quantitative reverse transcription polymerase chain reaction assays were done on an ABI Prism 7000 (Applied Biosystems, Foster City, CA) using 2× SYBR Green Master Mix (Applied Biosystems). Primer pairs were: c-fos: forward 5′-AACGGAGAATCCGAAGGGAA-3′; reverse 5′-GATTGGCAATCTCGGTCTGC-3′; glyceraldehyde-3-phosphate dehydrogenase: forward 5′-AGTTCAACGGCACAGTCAAG-3′; reverse 5′-GTGGTGAAGACGCCAGTAGA-3′.

Statistical Analysis.

Significance of differences between PHx and sham was determined by two-tailed Student t test assuming equal sample variance.

Results

Adenine Nucleotide Changes in the Regenerating Liver.

PHx brought about an instantaneous and marked decline in ATP levels in the remnant tissue. Analysis of the initial kinetics of changes in adenine nucleotide levels in freeze-clamped remnant livers revealed a 25% drop in ATP as early as 15 seconds after PHx from the control level of 2.76 ± 0.07 μmol/gww (Fig. 1A, Supplemental Table S1). ATP levels reached a low of 1.44 ± 0.12 μmol/gww by 30 seconds, with partial recovery by 2 minutes to a new steady state of 1.8 to 2.0 μmol/gww. ATP remained low throughout the replicative phase, and full recovery to control values was not seen until 72 hours after PHx.

Figure 1.

Adenine nucleotide changes in remnant livers following 70% PHx or Sham surgery. Livers from PHx (black circle) or sham (white circle) operated rats were freeze-clamped at designated postoperative times and processed for adenine nucleotide analysis. (A) ATP; (B) ADP; (C) AMP; (D) Total adenine nucleotides, TAN; (E) ATP/ADP. For estimates of statistical significance, PHx and sham livers from 4 to 13 animals were compared for each time point (Supplemental Table S1); **P < 0.01, *P < 0.05.

The decline in ATP was not associated with a corresponding increase in adenosine diphosphate (ADP) and adenosine monophosphate (AMP). ADP levels generally did not change significantly after PHx (Fig. 1B). AMP rose by 70% over control levels to 0.35 ± 0.03 μmol/gww by 15 seconds and remained elevated for at least 48 hours (Fig. 1C). Consequently, the total adenine nucleotide (TAN) content in remnant livers fell in parallel with ATP (Fig. 1D). By 30 seconds, TAN levels were at a minimum (27% below control) and did not recover to sham-operated levels until 3 hours after surgery (Supplemental Table S1). We did not detect an accumulation of adenosine, inosine, or inosine monophosphate (data not shown). As a result of these changes, the ATP/ADP ratio in the remnant liver, an indicator of the energy status of the liver, dropped immediately to 1.22 ± 0.09 from a control ratio of 2.57 ± 0.08 and remained low through 48 hours, recovering to control levels by 72 hours (Fig. 1E, Supplemental Table S2). Importantly, the adenylate kinase mass action ratio, [ATP][AMP]/[ADP]2 remained unchanged (0.4-0.5) in the livers of all animals, PHx or sham-operated, throughout the 72-hour postsurgical period (Table S2), indicating that adenylate kinase near-equilibrium is maintained despite substantial changes in adenine nucleotides.17

Sham surgery affected adenine nucleotide levels only modestly and briefly (Fig. 1, Supplemental Table S1). ATP content dropped slightly (9%) 1 minute after sham surgery, whereas ADP and AMP rose by 25% and 33%, respectively, with no change in total adenine nucleotide levels. Meaningful earlier time points for sham surgery could not be obtained (see Materials and Methods). However, the absence of major differences in adenine nucleotide levels between the untreated control and 1-minute sham surgery samples demonstrates that the control tissue obtained from untreated animals is an appropriate basis for comparison for the early PHx time points. Adenine nucleotides of sham-operated livers had returned to control levels by 2 minutes after surgery and remained unchanged throughout the postoperative period.

Adenine Nucleotide Changes Are Not Due to Mitochondrial Defects.

Mitochondrial oxidative phosphorylation is the predominant ATP-producing process in hepatocytes. Few data are available on mitochondrial function during the first 12 hours of regeneration. To assess whether persistent defects in mitochondrial function could contribute to the sustained changes in adenine nucleotide levels after PHx, we characterized the capacity for oxidative phosphorylation in mitochondria isolated from PHx and sham-operated rats 3, 6, and 12 hours after surgery. No significant differences were observed between these preparations in state 3 and state 4 respiration rates, respiratory control ratio, P/O ratio, and membrane potential (ΔDΨ), using either succinate or glutamate/malate as substrates (Supplemental Table S3). The data did not provide evidence of mitochondrial defects associated with a permeability transition or uncoupling of oxidative phosphorylation. We did not detect uncoupling protein expression in rat liver after PHx (not shown), as had been reported for mice.12 Thus, these data demonstrate that the observed decline in cellular ATP levels is not attributable to a defect in mitochondrial respiratory capacity or coupling that is preserved during the mitochondrial isolation procedure.

An important indicator of the balance of energy supply and demand in vivo is the redox potential of the nicotinamide adenine dinucleotide (NAD) couple in the cytoplasm and mitochondria.14 The decline in ATP/ADP in the remnant liver would result in increased electron transport and a more oxidized state of mitochondrial and cytoplasmic NAD, unless compensated by changes in substrate supply. (The concentration of inorganic phosphate in the cell would also affect the impact of changes in ATP/ADP ratio. However, in our experiments inorganic phosphate levels in liver extracts were increased or remained unchanged after PHx [data not shown].) The redox state of the free NAD couple (i.e., the ratio of free NAD to free NAD+ in the cytosolic and mitochondrial compartments is reflected in the lactate/pyruvate (L/P) and β-hydroxybutyrate/acetoacetate (BHB/AcAc) ratios, respectively.14

L/P ratios in regenerating livers rose 2-3–fold over those in sham animals by 15 minutes after PHx, reaching a plateau between 30 minutes and 3 hours before returning to sham levels by 6 hours (Fig. 2A). This increase arose from a more than 50% drop in pyruvate (0.21 ± 0.03 to 0.096 ± 0.016 μmol/gww in control and 15 minutes after PHx, respectively), whereas lactate remained unchanged (1.3 ± 0.3 and 1.1 ± 0.1 μmol/gww in control and 15 minutes after PHx, respectively, Supplemental Table S4). Thus, the change in the L/P ratio did not reflect a decreased capacity of the remnant liver to process lactate released from peripheral tissues, but is attributable to an increased cytosolic NADHfree/NADmath image. In sham-operated animals, the L/P ratio remained unchanged throughout 72 hours.

Figure 2.

Lactate/pyruvate ratios (L/P) and β-hydroxybutyrate/acetoacetate (BHB/AcAc) ratios in remnant livers after 70% PHx or sham surgery. Metabolite levels were analyzed in neutralized extracts from remnant livers of PHx and sham-operated rats. (A) L/P ratios for PHx (black circles) and sham (white circles). (B) BHB/AcAc ratios for PHx (black squares) and Sham (white squares). For estimates of statistical significance, PHx and sham livers from three to seven animals were compared for each time point (see Supplemental Table S4); **P < 0.01, *P < 0.05.

The redox state of mitochondrial NADHfree-NADmath image, reflected in the BHB/AcAc ratio, rose transiently, with peaks at 30 seconds and 6 hours, returning to sham levels by 12 hour (Fig. 2B). These changes were attributable almost entirely to increased BHB (Table S4). Because BHB is a terminal metabolite in a dead-end pathway (i.e., BHB is formed only from acetoacetate and is not further metabolized in liver), these changes in BHB/AcAc ratio likely reflect an increased mitochondrial NADHfree/NADmath image ratio. Thus, BHB/AcAc changes over the 24-hour period after PHx showed no evidence of a more oxidized state of NAD in mitochondria, despite a significant and sustained decline in ATP/ADP. These findings suggest that any increased energy demand in the remnant liver is met effectively by mitochondrial substrate supply and oxidative phosphorylation.

Adenine Nucleotide Changes After 30% Partial Hepatectomy.

Further experiments were designed to assess adenine nucleotides changes after PHx under conditions in which the demand for energy was varied. Excision of a smaller (30%) fragment of the liver (PHx30) gives a much reduced proliferative response18 and a proportionally reduced metabolic demand on the remnant liver. Remarkably, changes in ATP content and total adenine nucleotide levels during the first 15 minutes after PHx30 were almost indistinguishable from those occurring after PHx70 (Table S5). Within 30 seconds of PHx30 ATP dropped 40% from a control of 2.76 ± 0.07 μmol/gww, with a further decline at 1 minute. By 5 minutes, the ATP contents after PHx30 and PHx70 were similar. In parallel with the drop in ATP after PHx30, an equally rapid decline in ATP/ADP occurred (Supplemental Table S5). Indeed, over a 12-hour period, ATP/ADP changes after PHx30 and PHx70 were largely indistinguishable (Supplemental Table S5). However, recovery of ATP/ADP to control levels occurred within 24 hours after PHx30, whereas 72 hours were required for recovery after PHx70 (compare Tables S1 and S5). Thus, although ATP content and ATP/ADP in the remnant tissue recovered more rapidly after PHx30 than after PHx70, the adenine nucleotide changes during the early postoperative period were not related to the mass of the remnant tissue.

Effects of Circulating Glucose on Adenine Nucleotide Changes After PHx.

A major contributor to the metabolic demand on the liver is the maintenance of blood glucose, which affects liver carbohydrate metabolism both directly (through the glucose transporter and glucokinase) and indirectly (through pancreatic and adrenergic hormones released in response to changes in circulating glucose). Hence, we imposed variations in circulating glucose levels as a means of varying the energy demand on the liver.

Blood glucose concentrations were measured during 1 hour after PHx and sham surgery in fed rats (Fig. 3). Sham-operated animals showed a marked increase in blood glucose (6.4 ± 0.1 mM to >12 mM) within 5 minutes of liver palpation, presumably a glycogenolytic response to the isoflurane anesthesia and surgical stress mediated by α-adrenergic stimulation. After PHx, blood glucose also rose, but the increase was diminished by two thirds compared with sham, peaking at 8.7 ± 0.5 mM 5 minutes after surgery. A similar blood glucose increase after PHx with simultaneous depletion of liver glycogen was reported by Paloheimo et al.19

Figure 3.

Blood glucose levels after 70% PHx and sham surgery. Fed PHx rats (white circles); 24-hour fasted PHx (white triangles) rats; fed sham-operated rats (black circles); phentolamine-treated (10 mg/kg, 30 minutes before surgery) PHx rats (white squares). Error bars indicate standard error of the mean for three to five animals for each condition. Where not shown, standard errors were less than the symbol size.

Thus, PHx did not generate an instantaneous demand for gluconeogenesis as reflected in blood glucose levels. Nevertheless, because blood glucose increased with a slower time course than the decline in tissue ATP, we investigated the impact of treatments that imposed a sustained hyperglycemia before PHx. Conversely, the hyperglycemic response to isoflurane anesthesia and surgical stress was avoided by 24-hour fasting before surgery (which largely depletes liver glycogen), or by treatment with the α-adrenergic antagonist phentolamine, which inhibits the activation of glycogenolysis.

Hyperglycemia was achieved by extrusion and palpation of the liver, similar to the procedure used for sham surgery, eliciting a glucose surge within 5 minutes that is sustained for over 1 hour (Fig. 3). PHx was performed after maximal elevation of blood glucose had occurred, and remnant livers were removed and freeze-clamped 1, 5, or 15 minutes later. Before PHx, ATP content was unchanged from euglycemic rats but TAN were slightly elevated (Fig. 4C, Supplemental Table S6). After PHx, ATP and TAN had decreased by 1 minute and remained such for the subsequent 15 minutes, similar to the pattern observed in euglycemic animals, although the ATP change in hyperglycemic rats was slightly tempered (Fig. 4A, C). By contrast, hyperglycemia markedly suppressed the early change in ATP/ADP that was evident in euglycemic animals after PHx (Fig. 4B). When hyperglycemia was obtained by intraperitoneal injection of glucose (385 mg/kg body weight), changes in ATP and TAN were very similar to those obtained by prior palpation of the liver (not shown). These experiments indicate that elevated blood glucose levels do not prevent the PHx-induced decline in total adenine nucleotides, but suppress the rapid changes in ATP/ADP in the remnant liver.

Figure 4.

Effect of circulating blood glucose on adenine nucleotide changes after PHx. (A) ATP content, (B) ATP/ADP, (C) total adenine nucleotide content, 0 to 15 minutes after 70% PHx, under euglycemic, hypoglycemic, and hyperglycemic conditions. Data obtained from three to five rats per treatment for each time point. **P < 0.01, *P < 0.05, comparing PHx and sham-operated animals.

Other conditions were designed to prevent PHx-induced glycogenolysis: Hepatic glycogen stores are severely depleted in rats fasted for 24 hours, and PHx did not induce an appreciable change in blood glucose from presurgical levels in these animals (Fig. 3). TAN levels were not significantly affected by 24-hour fasting; however, ATP was decreased by 12%, and the ATP/ADP ratio was significantly lower compared with fed animals (Fig. 4A, B). PHx-induced changes in ATP/ADP ratio in the remnant livers of fasted rats were similar to those observed after PHx in fed rats. A marked decline in TAN was also observed in fasted animals, but was slower in onset, reaching the characteristic lower steady-state level by only 5 minutes after PHx (Fig. 4C).

More distinct effects were evident in fed animals pretreated for 30 minutes with the α-adrenergic antagonist phentolamine (10 mg/kg). Phentolamine pretreatment completely suppressed the rise in blood glucose in partially hepatectomized animals, and blood glucose was maintained at 6.3 mM or below for at least 1 hour after surgery (Fig 3).

Unexpectedly, phentolamine treatment had a marked effect on the changes in adenine nucleotides after PHx. The ATP content at 1 and 30 minutes after PHx was only slightly depressed in livers of phentolamine-treated rats and returned to the presurgical level by 60 minutes (Fig. 5A, Supplemental Table S7). The pronounced drop in total liver adenine nucleotide content after PHx was completely prevented by phentolamine treatment (Fig. 5C). Indeed, by 60 minutes, TANs exceeded presurgical levels (4.82 ± 0.37 μmol/gww). However, a postsurgical decrease in ATP/ADP ratio still occurred, because of substantial increases in ADP (Fig. 5B, Supplemental Table S7). Thus, although phentolamine treatment prevented the PHx-induced surge in blood glucose and the changes in ATP/ADP were compatible with increased energy demand, the α-adrenergic blockade also interfered with the PHx-associated decline in TANs. These findings demonstrate unequivocally that the loss of TAN immediately after PHx is distinct from the increased energy demand on the remnant liver.

Figure 5.

Effect of phentolamine treatment on adenine nucleotide changes after PHx. (A) ATP content, (B) ATP/ADP ratio, (C) total adenine nucleotide content, 0 to 15 minutes after 70% PHx in phentolamine-treated rats (10 mg/kg, 30 minutes before surgery). Data represent three to five rats per treatment for each time point. **P < 0.01, *P < 0.05, comparing phentolamine-treated and control animals.

Role of ATP Release in Early Signaling Responses Initiating Regeneration.

If phentolamine treatment prevents the PHx-induced ATP loss, it can serve as a tool to explore the role of ATP release in the early signaling events associated with onset of liver regeneration. Previous studies20 had demonstrated that treatment with α1-adrenergic antagonists inhibits cell cycle progression and DNA replication in vivo. The α-adrenergic antagonist phentolamine also inhibits characteristic early signaling responses associated with the priming phase of liver regeneration. Jun N-terminal kinase (JNK) phosphorylation, which occurs within 15 to 30 minutes of PHx, is a critical step in priming of the liver for regeneration and is one of the early cell signaling events contributing to the activation of immediate–early gene expression. Phosphorylation of JNK was almost completely inhibited by pretreatment of the animal with phentolamine (Fig. 6A, B). In addition, phosphorylation of c-Jun protein at S63, a critical serine residue that is a target for JNK, was inhibited by phentolamine (data not shown). Expression of the immediate–early gene c-fos, which normally peaks within 15 to 30 minutes after PHx, was also suppressed by phentolamine (Fig. 6C). We further tested whether ATP release contributes to these early signaling events by activation of purinergic receptors. Pretreatment of the animals with the purinergic antagonist suramin (100 mg/kg body weight) did not prevent the PHx-induced loss of ATP (ATP 2.02 ± 0.06 μmmol/gww, TAN 3.62 ± 0.20 μmol/gww 1 minute after PHx in suramin-treated animals (n = 3), not significantly different from untreated PHx animals), but inhibited JNK phosphorylation (Fig. 6A, B) and partly suppressed the c-fos expression at 30 minutes after PHx (Fig. 6C).

Figure 6.

Effect of phentolamine and suramin treatment on JNK phosphorylation and c-fos expression in remnant livers after PHx. (A) Western blots of phospho-JNK(p54) and JNK(p54) protein levels in liver extracts from untreated animals that did not undergo surgery (lanes 1-2) and control (lanes 3-5), phentolamine-treated (lanes 6-8), or suramin-treated (lanes 9-11) animals subjected to PHx (upper blots) or sham (lower blots) surgery. Inhibitors were injected intraperitoneally 30 minutes before surgery, and tissues were harvested 30 minutes after surgery. Control animals received a corresponding volume of saline. (B) Effect of phentolamine or suramin treatment on JNK phosphorylation after PHx or sham surgery. Densities obtained from western blots shown in (A) for phospho-JNK were normalized to total JNK protein in each sample,. **P < 0.01. (C) Effect of phentolamine or suramin treatment on c-fos relative to glyceraldehyde 3-phosphate dehydrogenase messenger RNA by quantitative reverse transcription polymerase chain reaction, expressed as ΔΔCt on a 2log scale comparing samples from PHx and sham surgeries. Samples were obtained 30 minutes after PHx or sham surgery, using three animals for each condition; **P < 0.01, *P < 0.05.

Discussion

One of the most striking findings revealed here is how rapidly metabolic parameters change in the remnant liver after PHx. The ATP content of the remnant liver declined by 25% within 15 seconds after PHx, and by 30 seconds had dropped to 50% below control levels (Fig. 1). After a partial recovery, steady-state ATP levels remained 20% to 30% below those of sham-operated animals through most of the regenerative period. Increases in ADP and AMP did not account for the drop in ATP, and TANs declined in parallel. A decrease in the ATP/ADP ratio is a predicted response to increased energy demand, but the rapid onset of this change is unexpected and suggests a sensing mechanism that immediately transmits information on the loss of functional liver mass to the remnant tissue. Other possible explanations for a drop in ATP/ADP, such as partial uncoupling, limited substrate supply, or inhibition of mitochondrial electron transport are not compatible with our data (Fig. 2, Supplemental Tables S3 and S4). Respiratory capacity and coupling of oxidative phosphorylation by isolated mitochondria were not affected for at least 12 hours after PHx, and there was no evidence of a shift toward a more oxidized state of mitochondrial or cytosolic NAD in the remnant liver. An early, transient increase in the BHB/AcAc ratio and a later, more sustained increase in the L/P ratio may indicate activation of the supply of metabolic substrates. Liver regeneration is known to mobilize fatty acids for oxidation19 but probably not yet at these early time points. Alternatively, TCA cycle activity may be stimulated to match the increased energy demand, for example, by intracellular Ca2+ changes elicited by α1-adrenergic or purinergic signals.21, 22

Glucose supply and ureagenesis are major metabolic functions that must be maintained during regeneration. In previous studies, blood glucose19 and urea levels23 were not markedly decreased after PHx, indicating that the liver meets the increased demand, despite a 70% decrease in liver mass. Our data support these findings. In both fed and fasted animals, the remnant liver appears able to supply metabolic energy to sustain major homeostatic functions. Importantly, the decrease in ATP levels after PHx was not primarily attributable to increased energy demand but reflected a net loss of adenine nucleotides. The mechanisms responsible for this loss are not entirely clear. Degradation of adenine nucleotides can occur either through dephosphorylation of AMP by 5′-nucleotidase, which generates adenosine, or through AMP deaminase to form inosine monophosphate, with subsequent degradation to inosine. However, the increase in AMP that could drive these reactions, although detectable, was relatively modest. We failed to detect a significant increase in AMP degradation products in liver extracts, suggesting that any such compounds were washed out or degraded further. Inhibition of nucleotide synthesis is unlikely to account for the rapid drop in TANs over such a short period. Alternatively, the ATP loss could have occurred without prior dephosphorylation. Shear stress is known to release ATP from isolated hepatocytes, and the increased blood flow through the remnant liver after PHx may have a similar effect.24 Recent studies demonstrated that ATP can be released from cells through a mechanism involving gap junction–related connexin hemichannels25, 26 or nonjunctional pannexin hemichannels.27 Hepatocytes express connexin-26, which forms anion-permeable hemichannels,28 as well as pannexin-1 (unpublished data). Regulators of hemichannel opening include both extracellular stress factors and intracellular signals (membrane potential, phosphorylation, and redox state).29

Importantly, the decrease in TANs is functionally distinct from the response to energy demand. Increased glycemia before PHx markedly slowed the changes in ATP/ADP without significantly altering TAN loss. By contrast, fasting or, more dramatically, pretreatment with the α-adrenergic antagonist phentolamine suppressed the loss of adenine nucleotides, but not the changes in ATP/ADP. These effects indicate that the decrease in liver TANs is controlled by signaling processes at least in part mediated through α-adrenergic receptors. Interestingly, protein kinase C and Ca2+ signals regulate gap junctional channel opening,30, 31 but whether this applies to connexin or pannexin hemichannels in the basolateral membrane remains unclear. It has long been recognized that an early signal must be involved in detecting the loss of functional liver tissue to initiate regeneration, but few studies have considered the time frame of seconds over which the onset of ATP depletion occurs. Such an early upstream signal may involve the mechanical stress associated with increased hemodynamic pressure after PHx. Phentolamine-induced vasodilation within the hepatic vascular bed likely attenuates the immediate hemodynamic changes incumbent on the remnant tissue, thereby ameliorating the mechanical stress experienced after PHx. However, phentolamine treatment would also suppress the activation of α1-adrenergic receptors on hepatocytes and prevent associated intracellular signaling events that may contribute to the metabolic responses observed in Fig. 4.

A rapid release of ATP (and possibly other cell constituents) after PHx could function as a paracrine signal that is recognized by purinergic receptors on neighboring cells. Stimulation of P2Y2 receptors in hepatocytes activates JNK, promoting induction of immediate–early genes and enhancing cell cycle progression and hepatocyte proliferation in vitro and in vivo.32 JNK is a central player in the onset of liver regeneration and is activated during the early priming phase after PHx,33, 34 promoting the G0–G1 transition in hepatocytes.35 Our data demonstrate that treatment with the purinergic antagonist suramin did not prevent PHx-induced ATP loss but inhibited JNK activation and c-fos expression. Additionally, nonparenchymal cells may be activated by purinergic signals.36 Kupffer cells are a potential source of cytokines that mediate priming after PHx, but the signals that activate cytokine release have not been identified. Purinergic stimulation may contribute to these responses.

Apart from a possible role of ATP (or its degradation products) as paracrine stress signals, the loss of adenine nucleotides would also change the intracellular milieu. Remarkably, TAN loss occurred within 30 seconds of PHx, but adenine nucleotide levels did not recover to sham levels until 24 to 48 hours, suggesting that the sensing mechanisms maintaining adenine nucleotide homeostasis were offset. One role for such an offset may be to signal the demand for metabolic energy. The major candidate for mediating such intracellular effects is the energy stress sensor AMP-activated protein kinase (AMPK). Although AMP levels in the liver were affected only modestly after PHx, the drop in ATP by itself causes a substantial decline in the ATP/AMP ratio (Supplemental Table S2). Intracellular AMP concentrations are within the range where AMPK activity could be affected by changes in ATP.37 Preliminary experiments suggest that the onset of liver regeneration is accompanied by a rapid activation of AMPK. However, the subsequent temporal profile of AMPK activity is complex, indicating that other factors contribute to maintaining low ATP levels through the replicative phase of regeneration.38

In summary, our data reveal that major changes in the functional state of the remnant liver occur within seconds of PHx, a time frame that until now was almost entirely unexplored. The characteristics of the adenine nucleotide changes observed in this early response phase indicate that energy demand only partially accounts for these effects and suggest that a loss of ATP occurs through a transient opening of nonspecific channels in hepatocyte plasma membranes. Inhibition of ATP release by the α-adrenergic antagonist phentolamine or inhibition of purinergic receptor activation by suramin prevented the activation of cell signaling pathways associated with the priming phase and suppressed the expression of the immediate-early gene c-fos. These findings strongly suggest that the release of ATP through this mechanism generates autocrine or paracrine stress signals to the remnant liver that contribute to the priming phase during the onset of regeneration.

Acknowledgements

The authors thank Christel Cordelier for technical support in aspects of this work.

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