Minocycline alleviates beta-amyloid protein and tau pathology via restraining neuroinflammation induced by diabetic metabolic disorder

Abstract

Background

Compelling evidence has shown that diabetic metabolic disorder plays a critical role in the pathogenesis of Alzheimer’s disease, including increased expression of β-amyloid protein (Aβ) and tau protein. Evidence has supported that minocycline, a tetracycline derivative, protects against neuroinflammation induced by neurodegenerative disorders or cerebral ischemia. This study has evaluated minocycline influence on expression of Aβ protein, tau phosphorylation, and inflammatory cytokines (interleukin-1β and tumor necrosis factor-α) in the brain of diabetic rats to clarify neuroprotection by minocycline under diabetic metabolic disorder.

Method

An animal model of diabetes was established by high fat diet and intraperitoneal injection of streptozocin. In this study, we investigated the effect of minocycline on expression of Aβ protein, tau phosphorylation, and inflammatory cytokines (interleukin-1β and tumor necrosis factor-α) in the hippocampus of diabetic rats via immunohistochemistry, western blotting, and enzyme-linked immunosorbent assay.

Results

These results showed that minocycline decreased expression of Aβ protein and lowered the phosphorylation of tau protein, and retarded the proinflammatory cytokines, but not amyloid precursor protein.

Conclusion

On the basis of the finding that minocycline had no influence on amyloid precursor protein and beta-site amyloid precursor protein cleaving enzyme 1 which determines the speed of Aβ generation, the decreases in Aβ production and tau hyperphosphorylation by minocycline are through inhibiting neuroinflammation, which contributes to Aβ production and tau hyperphosphorylation. Minocycline may also lower the self-perpetuating cycle between neuroinflammation and the pathogenesis of tau and Aβ to act as a neuroprotector. Therefore, the ability of minocycline to modulate inflammatory reactions may be of great importance in the selection of neuroprotective agents, especially in chronic conditions like diabetes and Alzheimer’s disease.

Keywords:

• diabetes mellitus
• minocycline
• tau protein
• β-amyloid protein

Introduction

Alzheimer’s disease (AD) is a neurodegenerative disorder that is characterized by progressive cognitive impairment. Histopathological hallmarks mainly indicate extracellular amyloid peptide deposition in neuritic plaques and intracellular deposits of hyperphosphorylated tau. Glucose metabolic disorders are probably an initiating factor.^1,2 A variety of mechanisms have been postulated in the risk of AD and diabetes mellitus (DM).^3,4 Some scholars have even proposed that AD is type 3 diabetes.^5,6 However, the relationship between DM and the process of AD remains elusive.

Minocycline, a tetracycline derivative, has a neuroprotective capability by limiting inflammation and oxidative stress.^7,8 Previously, we have found that minocycline can downregulate β-amyloid protein (Aβ) in the hippocampus, caused by diabetic metabolic disorder through inhibition of nuclear factor-κB pathway activation.⁹ In addition, several studies from our group have also evidenced that minocycline improves cognitive impairment triggered by both cerebral ischemia and diabetic metabolic disorder.^9–11 It is well accepted that the neuroinflammation induced by diabetic disorder plays an important role in Aβ production and the hyperphosphorylation of tau.^12,13 To further evaluate the neuroprotective role of minocycline in the diabetes related neurodegenerative process of AD, the present study was implemented to detect levels of tau and Aβ proteins in the brain of a DM model established by high fat diet and intraperitoneal injection of streptozocin (STZ), and observe the effects of minocycline on the inflammatory markers and levels of tau and Aβ proteins. These results noted that minocycline decreased the levels of the inflammatory markers and Aβ, and inhibited the hyperphosphorylation of tau in the hippocampus of rats with DM. This study suggests that minocycline can reduce neuroinflammation, and then lowers the hyperphosphorylation of tau and the level of expression of Aβ.

Methods

Animals and minocycline administration

Thirty-six Sprague-Dawley rats (10-month-old, female, body weight 200–250 g from the Third Military Medical University for Animal Field Hospital, Chongqing, People’s Republic of China) were fed with high fat and high sugar for 2 months (food composition: 10% lard, 20% sucrose, 2.5% cholesterol, bile salt 1%, 6.5% conventional food) to induce the onset of insulin resistance,¹⁴ and the diabetes model was established by 50 mg/kg intraperitoneal injection of streptozocin (STZ) (Sigma Chemical Co, St Louis, MO, USA) after the 2 month high fat and high sugar feed.^9,15 Animals were randomly divided into a control model group (subdivided into 4, 6, and 8 weeks after establishment of diabetes, with 6 animals per subgroup) and a minocycline intervention group (subdivided into 4, 6, and 8 weeks after minocycline intervention, respectively, with 6 animals per subgroup). Minocycline was administered by gavage on the same days as the STZ injection. The investigation conformed to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No 85–23, revised 1996).¹⁶ The animal experiments were performed according to internationally followed ethical standards and approved by the research ethics committee of Chongqing Medical University, Chongqing, People’s Republic of China.

Minocycline (100 mg/capsule, made by China Huishi Pharmaceutical Limited Company, People’s Republic of China) was dissolved into 0.5 mg/mL density with saline. The animals in the minocycline intervention group were executed through gavage via the stomach by 50 mg/kg/day of minocycline. Diabetic rats were administered the same volume of buffer by douche via the stomach. The minocycline dosage was determined according to the previous studies.^9,17 Minocycline was administered by gavage 2 days after STZ injection.

Enzyme-linked immunosorbent assay (ELISA)

A 500 pg/mL solution was prepared as manufacturer’s instruction and a standard curve created using computer software (Microsoft Excel [version 2010], Microsoft, Redmond Washington, USA) capable of generating a four parameter logistic curve fit. Rat hippocampus tissues were dissected and homogenized in tissue protein extraction reagent buffer (Biosource International, Inc, Camarillo, CA, USA). The analysis of Aβ by ELISA was conducted. Aβ inhibitors and 4-benzenesulfonyl fluoride hydrochloride (Sigma Chemical Co,) were added to tissue lysates to prevent degradation of Aβ. The concentration of Aβ_40/42 was measured using the Aβ₄₀ or Aβ₄₂ Colorimetric ELISA kit (Biosource International, Inc) according to the manufacturer’s instruction.

Western blotting

Samples were collected in the presence of protease inhibitors. After homogenization, the lysates were centrifuged at 100,000 × g, and the supernatants were saved for western blot. Equal amounts of lysates were subject to sodium dodecyl sulfate polyacrylamide gel electrophoresis (Tris-glycine mini gel; 1:2500; Biosource International, Inc) and western blot analysis using antibodies specific for the following: interleukin (IL)-1β, tumor necrosis factor (TNF)-α, Aβ precursor protein (APP), and tau proteins. The optical densities of the specific bands were measured by image analysis software (HPIAS 2000, Tongji Qianping Company, Wuhan, People’s Republic of China).

Immunohistochemical assay

Avidin-Biotin Complex (ABC) method is a standard IHC method and a widely used technique for immunhistochemical staining. Avidin, a large glycoprotein, can be labeled with peroxidase or fluorescein and has a very high affinity for biotin. Biotin, a low molecular weight vitamin, can be conjugated to a variety of biological molecules such as antibodies. The second antibody, a goat anti-mouse immunoglobulin (Ig) labeled with biotin, was from Vector Laboratories, Burlingame CA, USA. The intensity of staining for each of two hundred cells was adjusted. Five grades distinguished the degrees of staining, which represented five reaction coefficients, respectively. The five products of every coefficient and the corresponding cell number were added up, which resulted in the value of a positive score. All slides were measured in duplicate. Those samples with a score over 10, or frequency over 5%, were considered as positive.

Statistical analysis

All statistical data were analyzed via the SPSS software for Windows 2000 (SPSS, Inc, Chicago, IL, USA). One-way analysis of variance was employed. A standard curve was used for analysis of ELISA results. P < 0.05 was considered as statistically significant.

Results

Minocycline decreased expression of Aβ but not APP

The ELISA results showed that the Aβ₄₀ levels were significantly decreased from 56.43 ± 7.03 pg/mg in the model animals to 26.03 ± 6.13 pg/mg of lysate in the minocycline administration (P = 0.0001), and Aβ₄₂ levels from 89.45 ± 9.28 pg/mg to 39.04 ± 6.03 pg/mg of lysates (P = 0.0003) (Figure 1A). However, the results by immunostaining indicated that minocycline intervention had no effect on APP (Figure 1B).

Figure 1 Assay of Aβ_40/42 and amyloid precursor protein.

Notes: (A) The levels of Aβ_40/42 proteins were measured by ELISA according to the manufacturer’s instruction. The expression of Aβ_40/42 protein in the minocycline treatment group was significantly decreased when compared with the control model group. *Denotes P < 0.01 versus control group. (B) The levels of amyloid precursor protein were measured by immunostaining (1:200, Biosource International, Inc, Camarillo, CA, USA). It seems that there is no significant difference between the control model group and the minocycline intervention group. *Denotes P > 0.05 versus control group. The model group was subdivided into M4, M6, and M8 for 4, 6, and 8 weeks after streptozocin injection, and the minocycline administration group into MT4, MT6, and MT8.
Abbreviations: APP, amyloid precursor protein; M4, M6, M8: 4, 6, and 8 weeks after establishment of diabetes; MT4, MT6, MT8: 4, 6, and 8 weeks after minocycline intervention; OD, optical density.

Minocycline decreased phosphorylation of tau

The previous results showed that minocycline restrained expression of Aβ that occurs in the central nervous system during abnormal glucose metabolism. To further explore the neuroprotective mechanism of minocycline in a diabetic state, total and phosphorylated tau proteins (a molecular marker of AD) were tested by western blotting or immunohistochemistry. The levels of total tau protein by western blotting or immunohistochemistry showed no significant change between control and the minocycline intervention group (Figure 2A). The levels of phosphorylated tau proteins, including pre-tangle marker phospho-tau antibody TG3 (pT231), intraneuronal tangle marker phospho-tau protein (Ser214, pS214), and extracellular tangle marker PHD finger protein-1 ([PHF-1] pS396/pS404), significantly decreased after minocycline treatment (P = 0.0001), when compared with control model animals (Figure 2B).

Figure 2 Assay for tau proteins.

Notes: (A) The levels of total tau protein (Bioss Co, Beijing, People’s Republic of China) by western blotting (1:200) or immunohistochemistry (1:100) showed no significant change between the control and minocycline intervention group. *Denotes P > 0.05 versus control group. (B) The levels of phosphorylated tau proteins by western blotting as expressed by the densitometry ratio of tau proteins to β-actin (mean ± standard deviation) were measured, including pre-tangle marker phospho-tau antibody TG3 (pT231), intraneuronal tangle marker phospho-tau protein (Ser214, pS214), and extracellular tangle marker PHD finger protein-1 (pS396/pS404). These results showed that the optical density value of phospho-tau proteins significantly decreased after minocycline treatment (P = 0.0001). pT231 (1:200), ps214 (1:200), ps396 (1:100), and ps404 (1:100) were purchased from Bioss Co, scale bar is 20 μm.
Abbreviations: OD, optical density; M4, M6, M8: 4, 6, and 8 weeks after establishment of diabetes; MT4, MT6, MT8: 4, 6, and 8 weeks after minocycline intervention; PHF-1, PHD finger protein-1.

Minocycline downregulated IL-1β and TNF-&#x003b1

Increasing research studies have supported that diabetes induced neuroinflammation plays a crucial role in tau and Aβ pathogenesis.^12,18,19 Whether such neuroprotective effects of minocycline on diabetic metabolism disorder are through inhibiting inflammation is still unclear. To clarify the academic hypothesis, the proinflammatory cytokines, IL-1β and TNF-α, were detected here by ELISA and western blotting. The results by ELISA showed that IL-1β levels significantly decreased from 56.32 ± 6.02 pg/mg in control model animals to 25.48 ± 6.35 pg/mg of lysates in the minocycline treatment group (P = 0.0005), while TNF-α levels were reduced from 42.43 ± 6.62 pg/mg in control model animals to 23.44 ± 6.52 pg/mg in the minocycline treated animals (P = 0.0001) (Figure 3A). Similar to the previous ELISA results, the levels of IL-1β and TNF-α, as measured by western blotting, were distinctly lower after minocycline treatment (P = 0.0001) when compared with control model animals (Figure 3B).

Figure 3 Assay of protein level of interleukin-1β and tumor necrosis factor-α.

Notes: (A) The levels of interleukin (IL)-1β and tumor necrosis factor (TNF)-α by enzyme-linked immunosorbent assay in the minocycline treatment group decreased more significantly than in the control model group. *Denotes P < 0.001. (B) The levels of IL-1β and TNF-α by western blotting, as expressed by the densitometry ratio of IL-1β and TNF-α to β-actin (mean ± standard deviation), was more evidently reduced in the minocycline treatment group than in the control model group. *Denotes P < 0.01 versus control model group.
Abbreviations: IL-1β, interleukin-1β; OD, optical density; TNF-α, tumor necrosis factor-α; M4, M6, M8: 4, 6, and 8 weeks after establishment of diabetes; MT4, MT6, MT8: 4, 6, and 8 weeks after minocycline intervention.

Discussion

STZ, a powerful alkylating agent used to develop animal models to study diabetes and associated complications, is particularly toxic to the insulin-producing beta cells of the pancreas in mammals via interfering with glucose transport and impacting glucokinase function. Diabetic models will be successfully established, which occurred with cataract, hyperglycemia, uric acid, diabetic nephropathy, and a blood glucose level equal to or above 150 mg/dL were identified as diabetic while the blood glucose level of normal rats varied between 50 to 135 mg/dL.^18,19 Diabetic animals were continually given a high fat and high sugar diet. This study demonstrated that minocycline inhibited tau phosphorylation and decreased Aβ protein to maintain neural function, and attenuated neuroinflammation under diabetic metabolism disorder, indicating the neuroprotective role of minocycline in AD via inhibiting neuroinflammation.

Minocycline, an antibiotic that effectively crosses the blood–brain barrier, has been found to have significant neuroprotective effects on cerebral ischemia disorders,^20,21 demyelinating diseases,^22,23 and especially in neurodegenerative disorders including amyotrophic lateral sclerosis,^24,25 AD,²⁶ Huntington’s disease,^27,28 and Parkinson’s disease.^26,29 Previously, the results from our group have demonstrated that minocycline improved cognitive impairment and retarded Aβ generation in the hippocampus caused by diabetic metabolic disorder, through inactivating the nuclear factor-κB pathway.⁹ Considering the critical role of tau and Aβ pathology in the progress of cognitive impairment,^30,31 it is possible that minocycline improves cognitive impairment via limiting tau hyperphosphorylation and Aβ pathology. On the basis of the finding that minocycline had no influence on beta-site amyloid precursor protein cleaving enzyme 1 in diabetic disorder, which determines the speed of Aβ generation,⁹ it seems that minocycline has no modification on APP, since the critical role in Aβ generation is through modulating APP processing, and minocycline has no influence on APP level in this study.

Literature has shown that the two classical histopathological hallmarks include amyloid plaques (extracellular Aβ deposition) and neurofibrillary tangles (intracellular deposits of hyperphosphorylated tau protein) in AD.^32–35 The hyperphosphorylation of tau plays an important role in the progress of AD. This study detected the levels of phosphorylated tau proteins, including pre-tangle marker phospho-tau antibody TG3 (pT231),^34,35 intraneuronal tangle marker phospho-tau protein (Ser214, pS214), and the extracellular tangle marker PHF-1 (pS396/pS404).^36,37 The results from this research found that minocycline strongly limited the phosphorylation of tau protein, including TG3 (pT231), pS214, and PHF-1 (pS396/pS404), but not total tau. These data implicate that one of the neuroprotective roles of minocycline is via the suppression of the tau phosphorylation.

A variety of research data supports that minocycline acts as the neuroprotector via inhibiting brain inflammation,^9,10 astrocyte reactivation,³⁸ microglia activation,^39–41 oxidative stress,^9,38 apoptosis,⁹ and extracellular matrix degradation.⁴² Two common pathophysiological mechanisms of diabetic damage include oxidative stress and inflammation. Increasing evidence suggests that TNF-α and IL-1β (the inflammation markers) participate in the progression of brain injury from diabetes.^43,44 To further explain the neuroprotective mechanisms of minocycline, TNF-α and IL-1β were measured. The decrease of TNF-α and IL-1β evoked by minocycline occurred in this investigation. Accordingly, minocycline decreased tau hyperphosphorylation and downregulated Aβ protein by restraining neuroinflammation from diabetes, while inflammation contributes to both the hyperphosphorylation of tau and Aβ generation.

Neuroinflammation may be responsible for neurodegeneration in vulnerable regions such as the hippocampus.^45,46 There is growing evidence that supports a prominent role of inflammation in the development of AD.⁴⁷ An important feature of AD is that the hyperphosphorylation of tau and Aβ deposit may trigger an active, self-perpetuating cycle of chronic neuroinflammation which serves to further promote the hyperphosphorylation of tau and Aβ generation.^48,49 Therefore, minocycline may lower the self-perpetuating cycle in the pathogenetic cascade of neurodegeneration in AD, indicating that minocycline aims at both mechanisms to be a beneficial agent in the prevention and treatment of AD.

This study has evaluated the influence of minocycline on tau protein and Aβ protein under diabetic disorder. Minocycline decreases the hyperphosphorylation of tau and Aβ production by inhibiting the process of neuroinflammation. Minocycline may also lower the self-perpetuating cycle between neuroinflammation and the pathogenesis of tau and Aβ to act as a neuroprotector, maintain neural function, and improve behavioral deficits under diabetic disorder. Accordingly, the ability of minocycline to modulate the inflammatory reaction may be of great importance in the selection of neuroprotective agents, especially in chronic procedures like AD. Hence, further studies exploring the effect of minocycline on these mechanisms may lead to better understanding and improvement of the role of treatment.

Acknowledgments

This study was supported in part by the Animal Center of Chongqing Medical University and research projects from the Ministry of Civil Affairs, People’s Republic of China (2008-47-3-02).

Disclosure

The authors report no conflicts of interest in this work.