The Skeletal Effects of Short-Term Triple Therapy in a Rat Model of Gastric Ulcer Induced by Helicobacter pylori Infection.

PURPOSE: Triple therapy is the standard therapy to eradicate Helicobacter pylori (H.pylori) infection. Chronic use of proton pump inhibitors (PPIs), a component of triple therapy, is associated with osteoporosis. However, the skeletal effects of short-term triple therapy containing PPI remain elusive. This study aims to determine the skeletal effect of short-term triple therapy in a rat model of gastric ulcer induced by H. pylori.
METHODS: Three-month-old male Sprague Dawley rats were assigned to normal control, H. pylori-inoculated group (negative control) and H. pylori-inoculated group receiving triple therapy consisting of omeprazole [2.035 mg/kg body weight (b.w)], amoxicillin (102.80 mg/kg b.w) and clarithromycin (51.37 mg/kg b.w) (n=6/group). H. pylori infection developed for four weeks after inoculation, followed by two-week triple therapy. At the end of the treatment period, femoral bones of the rats were harvested for analysis. Bone mineral density and content of the femurs were determined using dual-energy X-ray absorptiometry, while bone strength was measured with a universal mechanical tester.
RESULTS: Bone mineral content was significantly lower in the negative control group compared to the triple therapy group (p=0.014). Triple therapy decreased strain (vs negative control, p=0.002) and displacement of the femur (vs normal control, p=0.004; vs untreated control, p=0.005). No significant difference was observed in other parameters among the study groups (p>0.05).
CONCLUSION: Short-term triple therapy increases bone mineral content but decreases bone strength of rats. Skeletal prophylaxis should be considered for patients on short-term triple therapy containing PPI.

Introduction

Helicobacter pylori (H. pylori) is a type of Gram-negative bacteria known to cause peptic ulcer disease and gastric cancer.1 H. pylori infection is also associated with extra-gastroduodenal diseases, such as metabolic syndrome, cardiovascular diseases and neurodegenerative diseases due to alternation in the immune system and low-grade inflammation.2 Since bone cells are sensitive to pro-inflammatory cytokines,3 chronic H. pylori infection could predispose a person to bone loss and osteoporosis. The relationship between H. pylori infection and bone health in humans has been contradictory so far. A recent meta-analysis showed that H. pylori increases the risk of osteoporosis [odds ratio (OR) 1.61, 95% confidence interval (CI) 1.11–2.32] but is not associated with significant variation in bone mineral density.4 The limited evidence so far does not show a conclusive association between H. pylori infection and fracture risk.5 The effects of H. pylori infection on bone strength could be derived from destructive mechanical test, so it is suitable to be investigated in an in vivo model.

Triple therapy is considered the first-line therapy in eradicating H. pylori. It consists of a proton pump inhibitor (PPI), clarithromycin and amoxicillin or metronidazole.6 PPIs suppress gastric acid secretion, creating a hypochlorhydric environment which does not favour the absorption of skeletal beneficial minerals like calcium, and vitamins like vitamin B.7 The associated increase in gastrin level also triggers histamine release which stimulates osteoclast formation.7 In our previous study, two-month pantoprazole treatment causes a significant trabecular microstructural deterioration in normal male rats, which is reversible by calcium supplementation.8 Others have demonstrated a significant decline in bone mineral density, increased bone resorption and decreased bone formation in rats treated with omeprazole for a few months.9–11 However, these models are not perfect as the animals are not infected with H. pylori. Besides, the data on short-term skeletal effects of triple therapy or PPI are very limited.

Thus, this study aims to determine the effects of 14-day triple therapy treatment on the bone of rat infected with H. pylori. The study is a secondary analysis of bone samples derived from a study that primarily aims to establish a rat model of H. pylori-induced gastric ulcer. We determined the bone health of the rats defined by densitometry and mechanical methods and hypothesised some degree of alternations associated with the infection and treatment. The information derived from this study will be important in deciding whether skeletal prophylaxis is necessary for patients on short-term triple therapy.

Materials and Methods

Bacteria Culture

H. pylori strain in the form of stock culture was obtained from the Department of Microbiology, Universiti Kebangsaan Malaysia Medical Centre. The bacteria were inoculated onto the Columbia blood agar and incubated microaerophilically with 10% oxygen gas, 10% carbon dioxide gas and 80% nitrogen gas for 5 days at 37°C.

Preparation of Treatment Agents

The triple agents were prepared by crushing clarithromycin (Noripharma, Selangor, Malaysia), amoxicillin (Duopharma, Selangor, Malaysia) and omeprazole (Y.S.P. Industries, Kuala Lumpur, Malaysia) into powder and dissolved in distilled water. The dose of drugs used in this experiment was converted from human suggested dosage using body surface conversion formula.6,12 The dose of clarithromycin [51.37 mg/kg (body weight) b.w], amoxicillin (102.80 mg/kg b.w) and omeprazole (2.035 mg/kg b.w) is equivalent to 500 mg, 1000 mg and 20 mg, respectively, for humans.

Treatment of Animals

Three-month-old Sprague Dawley male rats (n=18) weighted between 200 and 250 g were provided by Laboratory Animal Resource Unit, Universiti Kebangsaan Malaysia (Kuala Lumpur, Malaysia). The rats were housed at the Animal Laboratory, Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia (Cheras, Malaysia) in ventilated plastic cages under standard condition (25±2°C, 14/10 hours dark/light cycle). The rats were given access to tap water and standard rat chow (Product No: 702P, Goldcoin Feedmills, Klang, Malaysia) ad libitum throughout the study period. The rats were randomised into three groups (n=6/group) after acclimatised for one week. Two groups (negative control and triple therapy group) were inoculated with H.pylori suspension (10⁸ CFU/mL) via oral gavage twice a day at an interval of four hours for seven consecutive days,13 and the rats were left for four weeks for gastric ulcer formation. Then, one of the infected groups was treated orally with triple therapy regimen consisting of omeprazole [2.035 mg/kg body weight (bw)], amoxicillin (102.80 mg/kg bw) and clarithromycin (51.37 mg/kg bw) for 14 days. The rest of the groups received distilled water to mimic stress due to oral gavage (Table 1).

Table 1

Treatment Regimens of the Rats

Group	Treatment
Normal control	Distilled water; oral gavage
Negative control	Distilled water; oral gavage
Triple therapy	Omeprazole (2.035 mg/kg b.w), amoxicillin (102.80 mg/kg b.w), clarithromycin (51.37 mg/kg b.w); oral gavage

The rats were weighed weekly using a digital balance. They were euthanised after 14 days of treatment using ketamine/xylazine overdose. Their femoral bones were harvested for analysis. The bones were cleaned of soft tissues and weighted. A digital calliper was used to measure the length and diameter of the femurs. The stomach of the rats was processed into paraffinised histological slides and stained with haematoxylin and eosin (H&E) to determine the absence/presence of gastric lesions, and Giemsa to determine the absence/presence of H.pylori. This study was performed in accordance with the Principles and Guidelines for Ethical Use of Laboratory Animals, Universiti Kebangsaan Malaysia, Malaysian Code of Practice for the Care and Use of Animals for Scientific Purpose (2015), and Malaysian Animal Welfare Act (Act 772). The protocol of this study was reviewed and approved by Universiti Kebangsaan Malaysia Animal Ethics Committee (approval code: FAR/PP/2016/ISA/28-SEPT./798-JAN.-2017-DEC.-2018).

Bone Densitometry

The left femurs of the rats were scanned at high resolution using dual-energy X-ray absorptiometry (Hologic Discovery QDR Wi densitometer, Hologic, MA, USA) to evaluate bone mineral content (BMC) and bone mineral density (BMD). All DXA scans were analysed using the manufacturer’s software (Hologic QDR-1000 System). The short-term in vivo coefficient of error of the machine is 1.4%.14

Bone Mechanical Strength Test

Three points bending test was performed on the femur to measure its mechanical strength. The test was conducted with a precision universal tester (Autograph AG-10kNG; Shimadzu, Kyoto, Japan) and Trapezium X material testing operation software. The femurs were supported by rounded edge-free notches with a 10 mm gap in between. A blunt-end aluminium roller stamp was lowered gradually (5 mm/min) until the strength of 1 N was achieved. The test was halted automatically when a loss of force >20 N or a linear change of 2 mm was detected. The Trapezium X software received the data and analysed the load (N), displacement (mm), stiffness (N/mm), stress (N/mm2), strain (%) and Young modulus (N/mm2).

Statistical Analysis

Shapiro–Wilk test was used to determine the normality of data. Comparison of body weight adopted a time × treatment design, thus was interpreted using mixed-design analysis of variance (ANOVA) with small effect analysis. Normally distributed parameters which involved end-point measurement were analysed using one-way ANOVA with post hoc pairwise comparison (Tukey’s or Dunnett T3). Data with skewed distribution were analysed using Kruskal Wallis test and Bonferroni test for pairwise analysis. All data were displayed as mean ± standard error of the mean. A p-value <0.05 was considered as statistically significant. Statistical analysis was conducted using Statistical Package for Social Sciences version 26 (IBM, Armonk, USA).

Results

There was a time effect on body weight (p<0.001) but the interaction between time and treatment was not significant (p=0.572). All groups experienced a significant increase in body weight with time (p<0.05). However, there was no significant difference in body weight among the groups at all time points (p>0.05) except during week 5 of the experiment, in which the body weight of the negative control group was lower than the triple therapy group (p=0.032) (Figure 1).

Figure 1

Comparison of the body weight between groups across the study period.

H. pylori infection for 4 weeks caused lesions on the gastric mucosa. Triple therapy eradicated the bacteria and preserved gastric mucosa integrity in infected rats. The H&E and Giemsa stained photomicrographs are presented in Figure 2.

Figure 2

Photomicrographs of the gastric mucosa of the rats. The haematoxylin and eosin stained micrographs of the negative control group show gastric mucosa lesion (red arrow), while the gastric mucosa is intact for the normal control and triple therapy group. The Giemsa stained micrographs of the negative control group show spiral bacilli in the mucosa layer (black arrows).

The physical indices of femoral bone are depicted in Figure 3. The femoral weight of triple therapy group was significantly higher than the normal group and negative control group (p=0.016). Besides, the femoral area was significantly lower in the negative control group compared to the normal control group (p=0.01). Femoral length (p=0.006), area (p=0.002) and diameter (p=0.005) were significantly higher in the triple therapy group compared to the negative control group. No significant difference in femoral bone mineral density was detected among the study groups (p>0.05). However, BMC of the negative control group was significantly lower than the triple therapy group (p=0.014) (Figure 4).

Figure 3

Femoral weight (A), length (B), area (C) and (D) diameter of the rats in different groups.

Figure 4

Bone mineral density (A) and bone mineral content (B) of the ex-vivo samples.

No significant difference was observed in force, strain and stiffness among the study groups. However, the triple therapy group exhibited significantly lower strain (p=0.002) and displacement (p=0.005) than the normal group in displacement. The displacement of the triple therapy group was also lower compared to the negative control group (p=0.004) (Figure 5).

Figure 5

Bone mechanical strength indices of the rats investigated using the three-point-bending test, which derives force (A), strain (B), stress (C), Young’s modulus (D), displacement (E), stiffness (F).

Discussion

The present study demonstrated that H. pylori infection did not affect bone mineral density/content and mechanical strength but significantly decreased femoral bone area compared to the normal control group. Triple therapy increased femoral weight, length, diameter and BMC, but reduced strain and displacement significantly compared to the negative control group.

Epidemiological studies on the relationship between H. pylori infection and osteoporosis have yielded heterogeneous findings so far, whereby positive15,16 and negligible associations17,18 have been reported. A recent meta-analysis showed that H. pylori infection was associated with osteoporosis [odds ratio (95% confidence interval): 1.39 (1.13–1.71)] but not significantly with BMD at the hip, lumbar and femur.4 The inflammatory and immune reactions due to H. pylori infection are proposed as the mechanism altering bone turnover and resulting in osteoporosis.18 In our study, H. pylori infection did not significantly affect femoral bone mineral density/content and strength except the femoral bone area. This finding might be due to the short period of infection.

Our study showed that two-week triple therapy increased BMC but not BMD compared to the negative control group. Since areal BMD is the mineral content in a given area of bone while BMC is the unadjusted mineral content,19 the significant difference observed might be related to the reduced femoral area observed in the negative control. The observation might not have significant biological importance since the mineral content per area did not significantly differ between groups. However, triple therapy significantly reduced displacement and strain of bone compared to the negative control. Changes in these two parameters reflect reduced ductility or the ability of the bone to deform to prevent fracture.20 Therefore, short-term triple therapy might predispose bone fracture.

There is no evidence associating the use of amoxicillin or clarithromycin with bone health so far. On the other hand, omeprazole is a stomach acid suppressor used to prevent stomach ulcer caused by H. pylori infection.6 PPIs have been reported to induce bone loss through two main mechanisms, namely hypergastrinemia and hypochlorhydria.7 The irreversible binding of PPI to H+/K+-ATPase of parietal cells reduces hydrogen ions and increases gastric pH.21 This event reduces somatostatin secretion from D-cells and increases gastrin secretion from G-cells, which in turn, stimulates hypersecretion of histamine from enterochromaffin-like cells.22 The increased circulating histamine stimulates differentiation of osteoclast precursors and bone resorption activity.23 Hypochlorhydria (reduced stomach acid) can reduce the intestinal absorption of minerals essential for bone health, like calcium. This event will trigger the secretion of parathyroid hormone to mobilise calcium storage in the bone through the resorption process,24,25 subsequently causing bone loss and increased fracture risk.26

Considering all evidence together, we suggest that short-term triple therapy containing PPI might reduce bone strength without altering BMD. Since bone strength is determined by factors beyond bone mass, such as bone microarchitecture/geometry,27 properties of organic matrix and mineral crystal, an in-depth investigation into the skeletal actions of PPI on these factors is warranted. Human cross-sectional studies demonstrated that chronic PPI use was associated with reduced trabecular BMD but not other bone geometry indices.28 A clinical trial showed that 8-week pantoprazole treatment increased deoxypyridinoline urine level associated with osteoclast activity in the subjects.29 In preclinical studies, PPI could decrease collagen production in lung and liver, but no studies have been conducted on bone.30

Several limitations were identified in our study. The primary aim of the study is to establish a rat model of H. pylori-induced gastric ulcer. Thus, the period of H. pylori infection and triple therapy treatment was not optimised to produce skeletal effects. Prolonging the infection or triple therapy might result in more severe bone changes. Characterisation of the cellular and molecular changes of the bone induced by H.plylori infection and triple therapy was not performed. These aspects would be explored in future studies. The photomicrographs show evidence of mucosal exfoliation resulted from tissue processing, so the readers should interpret the images with cautions.

Conclusion

Short-term H. pylori infection did not alter bone health significantly, but a two-week course of triple therapy consisting of clarithromycin, amoxicillin and omeprazole lowers bone ductability without affecting the femoral BMD in the rats. Cellular and mechanistic changes of the bone need to be characterised to understand the effects of triple therapy on bone health. In line with our observation, patients on short-term triple therapy containing PPI should consider prophylaxis such as calcium and vitamin D supplements to protect bone health.