Protective effects of luteolin on nephrotoxicity induced by long-term hyperglycaemia in rats

Experimental drugs and instruments

Luteolin was purchased from Shanghai Tongtian Co., Ltd. (Shanghai, China), with a purity of more than 98%. A suspension of luteolin powder was prepared with normal saline and the concentration was approximately 20 mg/kg. Streptozotocin (STZ) was purchased from Sigma (Saint Louis, MO, USA). STZ was prepared as a 1% solution in 0.1 M of citrate buffer (pH, 4.0–4.5). Primary antibodies and appropriate secondary antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Anti-caspase-3 and anti-Nphs2 antibodies were obtained from Abcam (Abcam, Cambridge, CB, UK). Ultrasound was performed by using the LOGIQ E9 in harmonic-contrast mode with the ML6-15 ultrasound probe (General Electric Company, Fairfield, CT, USA). We used the instrument’s built-in wash in/wash out mode to analyse the contrast results. Contrast agent (SonoVue) was purchased from Bracco Co., Ltd. (Milan, Italy).

Laboratory animals

The experiments were approved by the Institutional Animal Care and Use Committee of Wenzhou Medical University. Male Sprague–Dawley rats, which were 7 to 8 weeks old, were purchased from SLAC Experimental Animal Co., Ltd. (Shanghai, China). The rats were fed in separate cages and ate freely in a well-ventilated environment, which provided suitable temperature and humidity. The rats were adapted to a 12-hour light/dark feeding cycle for 1 week.

Preparation of the experiment

Fifty-three mice were randomly divided into the control group (n = 6), the model group (diabetic group; n = 23), and the experimental group (LUT + diabetic group; n = 24). The mice were fasted for 12 hours before modelling, and each mouse was intraperitoneally injected with STZ 65 mg/kg. On days 3, 7, and 14 after STZ injection, fasting blood glucose levels were determined from blood collected from the tail vein using an autoanalyser (Surestep, Roche, Germany). Only the rats that survived with fasting blood glucose levels exceeding 16.7 mmol/L, excessive drinking, eating and polyuria, and weight loss were diagnosed with diabetes. Age- and sex-matched control rats were injected with STZ-free citrate buffer. Because of physical problems, 13 rats died, including eight rats in the diabetic group and five rats in the LUT + diabetic group. Two rats failed to achieve the model criteria. The remaining mice were monitored for survival time.

Intragastric administration

One week after successful establishment of the diabetic model, the LUT + diabetic group had intragastric administration of luteolin 20 mg/mL with a dose of 80 mg/kg daily for 8 weeks. The control and diabetic groups were provided a corresponding dose of normal saline. During the treatment period, five rats in the model group died because of fighting, intolerance of the high-glucose state, and a weak physique. Additionally, two rats in the LUT + diabetic group died because of improper intragastric administration.

Blood glucose monitoring

Starting on the fourth week of intragastric administration, the tail vein blood of rats was collected every weekend to measure the random blood glucose level.

Ultrasonic examination

After 8 weeks of treatment, the rats were anaesthetized with 0.3 mL/kg 10% chloral hydrate and fully shaved to exposed the kidney area. The rats were then placed in a prone position. The length, width, and thickness of the maximum coronal sections of the right kidneys were measured, and the renal volume was calculated according to the following formula: kidney volume (cm³) = (π/6) ×length (cm) × width (cm) × thickness (cm). Additionally, the colour Doppler mode was used to observe the distribution of right renal blood flow, and the spectral Doppler mode was used to record haemodynamic parameters, such as peak systolic velocity (VS), end-diastolic velocity (VD), and main artery and interlobar arterial resistance indices (RIs). Contrast agent was injected into the tail vein to obtain a contrast-enhanced ultrasound image. Changes in renal cortical contrast agent echo intensity were then observed in real time for 2 minutes (mechanical index =0.08, 4.5–7.5 MHz, depth = 2–3 cm). All images were stored as digital imaging and communication in medicine format images in the hard disk built into the ultrasound machine. The echo of contrast agent microbubbles in the region of interest (ROI) (superficial peripheral renal cortex) was analysed by quantitative ultrasound analysis software (wash in/wash out) to generate the contrast agent TIC. Some quantitative parameters can be obtained from the real-time CEUS TIC curve, such as the absolute peak intensity, time to peak (TTP), area under the curve, and gradient from the start frame to the peak frame (Grad). The TTP indicates that the contrast medium begins to enter the ROI after reaching the peak intensity. The gradient response indicates the tissue perfusion rate, and absolute peak intensity indicates the cross-sectional area of the contrast medium with the most obvious enhancement of signal intensity. This value reflects the blood volume of local tissue and can reflect perfusion of the kidney. There is a good correlation between local tissue blood flow and area. Each site within the ROI was repeatedly analysed three times and the average was calculated. The TIC curve can sensitively reflect perfusion of small renal vessels.

Renal function test

After the last administration session, the rats were anaesthetized with 0.3 mL/kg 10% chloral hydrate. Blood was taken from the abdominal aorta. Serum was obtained by centrifugation of the blood at 1000 × g at 4°C for 10 minutes before storage at −20°C. Serum creatinine (Scr), blood urea nitrogen (BUN), total cholesterol (TC) and triglyceride (TG) levels were measured.

Haematoxylin–eosin staining of the kidneys

After intragastric administration at the eighth week, the rats in every group were killed by the perfusion method, and both kidneys were removed. Body weight and kidney weight were measured. Right kidney tissue was fixed with 4% paraformaldehyde. After dehydration with graded alcohol solutions and immersion in xylene, the samples were embedded in paraffin. The paraffin blocks were cut into 5-µm-thick sections and kidney slices from the three groups were obtained. Kidney slices were then deparaffinized in xylene and rehydrated through graded alcohol solutions before haematoxylin–eosin staining using a standard protocol. The samples were analysed by optical microscopy (Nikon ECLPSE 80i; Nikon, Tokyo, Japan) to observe mesangial cell proliferation.

Immunohistochemical staining of caspase-3 and Nphs2 protein

After paraffin-embedded sections were deparaffinised and rehydrated, the sections were incubated with 3% H₂O₂ for 10 minutes at 37°C and then blocked with 5% bovine serum albumin for 30 minutes at 37°C. The sections were covered with rabbit anti-rat polyclonal primary antibody caspase-3 or Nphs2 (1:200) and stored at 4°C overnight. The samples were incubated with the goat anti-rabbit secondary antibody for 1 hour. The samples were then stained with 3,3-diaminobenzidine (1:20) and counterstained with haematoxylin. The positive points were dyed brown and observed using optical microscopy (ECLPSE 80i; Nikon).

Transmission electron microscopy

Tissue blocks of approximately 1 × 1 × 1 mm were removed from the left kidney and fixed with 2.5% glutaraldehyde solution. The tissue was stored at 4°C for preparation of transmission electron microscopy specimens. After preparation of the specimens, the specimens were sliced by an ultra-thin slicer (Hitachi Co., Ltd., Power-town XI, Tokyo, Japan) and observed by a transmission electron microscope (H-7500; Hitachi Co., Ltd.). Proliferation in the glomerular basement membrane (GBM) and mesangial matrix, and the loss of podocytes and other pathological changes were observed under transmission electron microscopy.

Two-dimensional ultrasound and Doppler ultrasound

Two-dimensional ultrasound showed that right renal volume in the diabetic group (2.593 ± 0.205) was significantly larger than that in the control group (1.734 ± 0.152, P < 0.01), but renal volume in the LUT + diabetic group (2.116 ± 0.416) was significantly lower than that in the diabetic group (P < 0.05, Figure 3). Moreover, the ultrasonic echo intensity of the renal cortex in the diabetic group was significantly higher than that in the control group (P < 0.05), and that in the LUT + diabetic group appeared to be higher (not significant) than that in the control group. However, the junction of the cortex and medulla was still clear in the LUT + diabetic group. VS and VD appeared to be lower in the diabetic group (not significant), while the RI was significantly higher (P < 0.01), compared with those in the control group. These parameters were better in the LUT + diabetic group than in the diabetic group, but only the RI was significant (P < 0.01).

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Figure 3.

Effect of luteolin on two-dimensional ultrasound and time intensity curve parameters. (a–d) Quantitative analysis of the volume, length, width, and thickness of the right kidney. (e–h) Quantitative analysis of the absolute peak intensity, area under the curve, time to peak, and Grad of the time intensity curve. Data are expressed as the mean ± standard deviation. *P < 0.05; **P < 0.01 vs. the control group; ^#P < 0.05 vs. the diabetic group. Grad: gradient from the start frame to the peak frame; LUT: luteolin.

Doppler ultrasound showed that the distribution of blood flow in the diabetic group was lower than that in the control group. Additionally, the distribution of blood flow in the LUT + diabetic group was more abundant than that in the diabetic group (Figure 4).

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Figure 4.

Right kidney size shown by two-dimensional ultrasound and renal blood signals from Doppler ultrasound.

Parameters of the TIC in contrast-enhanced ultrasound

Asymmetric single-peak TICs are shown in Figure 5a. The TIC curve in the control group showed a rapid upward trend and slowly decreased after rising to a peak. The rising branch of the TIC in the diabetic group was slower than that in the control group, and it slowly decreased after a few seconds of plateauing after the peak. The quantitative perfusion parameters from the TIC in the three groups of rats are shown in Figure 3e–h. The absolute peak intensity, area under the curve, Grad, and TTP values in the diabetic group were greater than those in the control group, but only the absolute peak intensity and area under the curve values were significantly different (both P < 0.05). This finding suggests that the absolute peak intensity and area under the curve are sensitive indicators reflecting haemodynamic changes that were characteristic of diabetes induced under hyperglycaemic conditions. Moreover, the absolute peak intensity and area under the curve values in the LUT + diabetic group were lower than those in the diabetic group, but only absolute peak intensity values were significantly different (P < 0.05). This finding suggests that absolute peak intensity values may be more sensitive than area under the curve values to haemodynamic changes.

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Figure 5.

(a) Contrast-enhanced ultrasound images and time intensity curves. (b) RI of the renal artery. Data are expressed as the mean ± standard deviation. **P < 0.01 vs. the control group; ^##P < 0.01 vs. the diabetic group. RI: resistance index; LUT: luteolin.

Haematoxylin–eosin staining

In the control group, the renal glomerulus was clear in structure and normal in shape, with no enlargement or atrophy, a smooth glomerular capsule, and no infiltration (Figure 6a). There was no thickening of the basement membrane, normal distribution of mesangial cells and extracellular matrix, and clear tubular structure of renal tubules. Glomeruli in the diabetic group were significantly atrophied and the lumen was enlarged compared with those in the control group. Additionally, mesangial cells were proliferated and the GBM was thickened. In some stained sections, dilatation of the renal tubular lumen, inflammatory cell infiltration, and vacuolar degeneration of renal tubular epithelial cells were also observed. Nevertheless, these pathological renal lesions were alleviated after treatment with luteolin.

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Figure 6.

Effect of luteolin treatment on renal structural changes, caspase-3 expression levels, and Nphs2 protein levels in the three groups. Red arrows indicate a glomerulus and orange arrows indicate caspase-3 expression. Brown areas are positive for caspase-3 expression in renal tissue. (a) Representative microphotographs of kidney sections from all three groups with haematoxylin and eosin staining (× 400). (b, c) Representative microphotographs of caspase-3 and Nphs2 expression with immunohistochemical staining (× 400).

Immunohistochemical staining

In the control group, there was little staining for caspase-3 in renal tissue (Figure 6b). Caspase-3 expression was higher in the glomeruli and the adjacent cortical tubule interstitium in the diabetic group compared with the control group. After luteolin treatment, caspase-3 levels were decreased. Figure 6c shows Nphs2 protein immunofluorescence staining. Nphs2 protein expression was distributed along the GBM. There was high Nphs2 protein expression in the control group, and a small amount of Nphs2 protein expression was found in the diabetic group. However, Nphs2 protein expression levels in the LUT + diabetic group were higher than those in the diabetic group. This result indicates that luteolin may preserve podocytes and reduce apoptosis to protect kidney function.

Pathological changes under electron microscopy

In the control group, the foot process in the mesangial area was long and distinct. In the diabetic group, we observed a high volume of glomeruli, thickness of a diffusely homogeneous GBM, and severe hyperplasia of the mesangial matrix in the mesangial area (Figure 7). Additionally, because of stimulation of podocytes by long-term glycoprotein, the structure of the foot process was unclear, and there was extensive fusion. The podocytes had changed from branch bifurcation to fusiform, and the bifurcation was obviously smaller, with some of them showing similarity to pebbles. A large number of glycogen deposits were also observed in other cells in the kidneys in the diabetic group. Vacuolization in the renal tubule was obvious. In the LUT + diabetic group, there was less GBM thickening, milder mesangial hyperplasia, and more scattered and focal foot process fusion compared with the diabetic group.

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Figure 7.

Representative renal sections of each group as shown by transmission electron microscopy with different magnifications. Red arrows indicate podocyte foot processes. Yellow arrows indicate the glomerular basement membrane (a: × 3000; b: × 8000; c: × 10,000). LUT: luteolin.