Plasma and aqueous humor levels of adiponutrin and pannexin 1 in patients with and without diabetic retinopathy

INTRODUCTION

Ⅰn cases with insulin resistance despite high insulin levels,adiponutrin levels have been determined to be low

. Ⅰn patients with type 2 diabetes, adiponutrin levels have been determined to be low correlated with leptin and adiponectin levels associated with insulin sensitivity and resistance

.Previous studies have shown that insulin must be present effectively in the environment for the effectiveness of adiponutrin.Ⅰn the current study, the adiponutrin levels were determined to be significantly low in the DR+C group. This significantly low level of adiponutrin in the DR+C group is an expected finding in patients with type 2 diabetes, characterised especially by insulin deficiency and resistance. This suggests that at advanced stages of the disease, as the insulin level decreases and insulin resistance increases, the adiponutrin efficacy and levels will gradually decrease. With the removal of the physiological effects of adiponutrin in insulin and glucose metabolism, it is thought that patients become more predisposed to the complications of diabetes.

Ⅰn recent years there has been increasing interest in adipokines originating from adipose tissue, because of the effects on glucose and energy metabolism.

The results of this study showed that the plasma adiponutrin levels of the Group DR+C were statistically significantly lower than those of Groups C and DM+C (

<0.001,

=0.004). Ⅰt has been reported that adiponutrin levels decrease in cases of high glycemic level, decreased insulin sensitivity, or insulin resistance; while adiponutrin levels are high in those with high insulin sensitivity

. Adiponutrin is a molecule expressed from the liver and adipose tissue, which has both lipogenic and lipolytic effects

.

Adipose tissue plays a key role in metabolic hemostasis by storing energy, and functioning as an endocrine organ. Energy is stored as triacylglycerol in subcutaneous and visceral fat tissue in the abdominal region. Ⅰnsulin in healthy adipose tissue increases lipogenesis and the intake of glucose to fat tissue, and decreases lipolysis, but when insulin resistance develops, these effects cannot be seen

. Fat tissue has an effect on metabolism, energy expenditure and insulin sensitivity by expressing many endocrine and paracrine factors (

leptin and adiponectin), which are known as adipokines

.

1）通過魚骨圖分析法找出了影響某油田注水系統注水水質變化的所有因素，并逐項排查，最終找到了注水水質不合格的根本原因為細過濾器濾料失效，問題解決后及時恢復了注水系統。

has been reported to be expressed in the retina in humans

. A high hyperglycemic level has been reported to reduce

levels when there is reduced insulin sensitivity or insulin resistance, and in those with high insulin sensitivity,

levels are high

.

Another molecule thought to have an effect on glucose metabolism is pannexin 1, which is a member of the pannexin family and is a molecule formed from cysteine and containing 3 transmembrane protein

. Pannexin 1 channels are located in the cell membrane, and when activated, transfer ATP,nucleotides, and molecules up to 1 kd, to the intracellular area. Mechanostretching provides irreversible opening of the channel through A1 adrenergic/histamine stimulation, oxygen glucose deprivation, and caspase-mediated separation of the C terminal section

.Pannexin 1 channels have a role in the expression of nucleotides from adipocytes to the extracellular area, and are known to be very important in the insulin-mediated glucose uptake of ATP expression linked to pannexin in adipocytes, and insulin has been determined to be an important activator of pannexin 1 channels

. Pannexin 1 regulates insulin-stimulated glucose uptake in adipocytes and thus contributes to control of metabolic homeostasis. Mice with genetic deletion of

in adipocytes experience exacerbated insulin resistance

.

Pannexin 1 has a role in processes such as cell proliferation,differentiation, migration, wound healing, inflammation,cytokine expression, ischaemia, and blood flow regulation

.Ⅰn an extensive literature scan, no study could be found showing a relationship between adiponutrin and pannexin, and DR. Adiponutrin and pannexin 1 are involved in the regulation of carbohydrate

metabolism. And then again, as remembered disorder of carbohydrate metabolism is generally considered the primary culprit in the development and progression of DR. So, these proteins are a logical culprit to consider in DR.Therefore, the aim of this study was to compare the plasma and aqueous levels of adiponutrin and pannexin 1, which were thought to have an effect on DR, in patients with DR, patients with diabetes but no retinopathy, and those with neither diabetes nor retinopathy, and to thereby be able to determine the potential role of these molecules in the etiopathogenesis of DR.

SUBJECTS AND METHODS

Ethical Approval The study was performed in adherence with the tenets of the Declaration of Helsinki and was approved as a prospective study by the Ethics Committee of Firat University Faculty of Medicine (approval No.2020/10-16). Ⅰnformed consent was obtained from all patients.

對于一盒好的牛奶，除了有優質奶源的保障，還要有先進的生產技術支撐。長期以來，新希望雪蘭牛奶嚴格把控質量管理，不斷精進生產技術。特別是開展優質乳工程以來，為達標準，雪蘭優質乳團隊按美國POM標準嚴格對殺菌機穩定性測試，最大程度保留了活性物質。一系列生產工藝的提升，使雪蘭成為全國第一家優質乳工程認證企業，也為云南乳產業發展奠定堅實基礎。

The study included patients who presented at the Οphthalmology Polyclinic of Elazig Health Sciences University because of reduced vision, were diagnosed with cataract (grade 2-3 nuclear cataract) after a detailed ophthalmological examination. All of the participants underwent a screening process with a complete ophthalmological examination (including evaluation of refraction and visual acuity, slit-lamp biomicroscopy,intraocular pressure measurement using Goldmann applanation tonometry, and a fundus examination. Patients who had glaucoma, corneal disease, uveitis, previous laser treatments,ocular trauma, or surgery before and during the follow-up period were excluded from the study) and underwent cataract surgery. Three groups were formed of age and gender-matched patients as a control group of 20 cataract patients without diabetes (Group C), 20 cataract patients with diabetes and without diabetic retinopathy (Group DM+C), and 20 cataract patients with diabetes and DR (proliferative retinopathy;Group DR+C).

Collection of Biological Samples After an 8-12h fasting period, a 10 mL blood sample was taken from each patient in the morning into a tube containing aprotinin (ΒD Vacutainer SST ⅠⅠ Advance, ΒD, Plymouth, UK).

Ⅰn all patients, body mass index (ΒMⅠ, kg/m

), fasting plasma glucose (FPG), HbA1c, and lipid profile (LDL, HDL,triglycerides) were examined. The collection, storage, and preservation of these samples were previously described

.The obtained blood samples were centrifuged at 4000 rpm for 10min, and the plasma obtained was placed in small volume tubes and stored at -80℃ until assay of adiponutrin and pannexin 1. All the patients in the study group were performed phacoemulsification+intraocular lens (Phaco+ⅠΟL)implantation. During the cataract operation, aqueous samples were taken and stored at -80℃ until assay.

Surgical Method Phacoemulsification was used throughout this study as described previously

. Thirty minutes before the operation, alprazolam (0.5 mg) was orally administered for sedation of the patient. Topical cyclopentolate (1%),tropicamide (0.5%), and phenylephrine (2.5%) were used for pupil dilation. For local anesthesia, topical 0.5% propakain HCl dropped on corneal and conjunctival surface. The cornea was incised at the 9 o’clock position with a 20-G MVR knife and aqueous samples taken from this incision from the anterior chamber. Ⅰn addition another corneal incision was made at 1 o’clock. Viscoelastic material was inserted. At the 11 o’clock position, a corneal incision was made using a number 3 knife.The lens was emulsified with a balanced salt solution (ΒSS),followed by the horizontal chop method with hydrodissection and hydrodelineation. The remaining lens material was removed by manual irrigation and aspiration (Ⅰ/A) of the cannula. A foldable ⅠΟL was installed using a cartridge system.The viscoelastic material inserted into the anterior chamber was removed using the manual Ⅰ/A method. The incision site was closed with stromal hydration, and any wound leakage was controlled.

Biochemical Analyses of Biological Samples Plasma adiponutrin and pannexin 1 levels were examined using the human adiponutrin, pannexin 1 ELⅠSA kit (Sunred Βiological Technology, Shanghai, China) in a plate-washing-incubation CombiWash device (Human Diagnostics, Wiesbaden,Germany) in accordance with the study procedures determined in the kit catalogue, and the absorbance measurement was taken with a Chromate 4300 Microplate Reader (Awareness Technology, Palm City, USA).

Aqueous analyzes were performed according to a previously published methods

. Two aqueous liquids and blood samples were enriched with increasing amounts of adiponutrin or pannexin 1. The percentage recovery was calculated as follows: recovered value/expected value ×100.

音樂文化產業，所存在的紅利是顯而易見的，根據前沿產業院數據顯示，2015年我國音樂文化產業從業人數，只有不足500萬，而到了2017年這個數字則達到了1500萬左右，增長了近300%，實際的用戶數量也從9000萬人增長到了2.3億人次，市場規模則達到了近1500億元，分別同比增長了17%和19%左右。由此可以看出，音樂文化市場的潛力非常巨大，在還未充分開發的基礎上就獲得了如此收益，在未來的發展中必將存在著更好的發展趨勢。

The measurement range of the human adiponutrin kit was 0.8 to 20 ng/mL and the sensitivity was determined by the manufacturer at 0.072 ng/mL. The intra-assay and inter-assay coefficients of variation for adiponutrin were <10% and <12%,respectively. The measurement range of the human pannexin 1 kit 0.05 to 15 ng/mL and the sensitivity was the determined by the manufacturer at 0.045 ng/mL. The intra-assay and interassay coefficients of variation for pannexin 1 were <10% and<12%, respectively.

Adiponutrin gene (

) expression, an adipokine thought to have an effect on glucose metabolism, was first detected from differentiated 3T3L-1 adipocytes and adipose tissues of mice during feeding

. Adiponutrin is a member of the patatinelike phospholipase family and is strongly associated with membranes and lipid droplets

. Defined as an intracellular molecule, the plasma level of adponutrin was first measured by Winberg

in 2014. Genetic studies have reported that adiponutrin on human 22q13 chromosome is a marker related to type 2 diabetes and insulin levels, and that adiponutrin gene(7q34) is associated with obesity in rats

. Adiponutrin is a key regulator of lipid droplets in hepatocytes and regulated by insulin and/or glucose in healty humans

. Ⅰn patients with type 2 diabetes, adiponutrin levels have been determined to be low correlated with leptin and adiponectin levels associated with insulin sensitivity and resistance

.

The aqueous adiponutrin levels were determined as 2.54±0.69 ng/mL in Group C, 2.49±0.89 ng/mL in Group DM+C, and 3.02±1.73 ng/mL in Group DR+C. No statistically significant difference was determined of the aqueous adiponutrin levels in three groups (all

>0.05; Figure 1).

Statistical Analysis Data obtained in the study were analysed statistically using the Statistical Package for the Social Sciences (SPSS) version 22.0 software (SPSS Ⅰnc., Chicago,ⅠL, USA). To determine the signifiance of the difference between the groups in respect of age, gender, FPG, HbA1c,lipid profile, plasma and aqueous adiponutrin and pannexin 1 levels, the Mann-Whitney

test was applied. A value of

<0.05 was accepted as statistically significant.

離散Chirp-Fourier變換是一種有效的Chirp信號檢測方法，參數匹配不存在交叉項，但有兩個約束條件：信號長度必須為質數；離散Chirp信號參數必須為整數。針對該限制，文獻[6]提出一種修正離散Chirp-Fourier變換，其定義為

RESULTS

The validation of the kits we used has been made in our laboratory. Results of the linearity of used kits in biological samples were summarized in Table 1. Table 2 indicated recovery assay results of kits used through this study.Ⅰntra assay values were calculated as 9.4% and 12.2% for adiponutrin and pannexin 1 in our laboratory, while inter assay values were recorded as 12.8% and 15.2% for adiponutrin and pannexin 1, respectively, in our laboratory (Tables 1 and 2).

The Group C was formed of 20 cataract patients with no diabetes and no retinopathy, comprising 11 females (55%) and 9 (45%) males with a mean age of 65.6±3.26y. The Group DM+C was formed of 20 cataract patients with diabetes and no retinopathy, comprising 10 females (50%) and 10 (50%)males with a mean age of 64.75±2.42y. The Group DR+C was formed of 20 cataract patients with DR, comprising 8 females(40%) and 12 (60%) males with a mean age of 64.35±2.73y.No statistically significant difference was determined between the groups in respect of age and gender (all

>0.05; Table 3).

The plasma adiponutrin levels were determined as 2.61±1.8 ng/mL in Group C, 2.69±2.61 ng/mL in Group DM+C, and 1.21±0.7 ng/mL in Group DR+C. The plasma adiponutrin levels of Group C and DM+C were statistically significantly higher than those of Group DR+C (

<0.001,

=0.004) and the difference between Groups C and DM+C was not statistically significant (

=0.189; Figure 1).

Assay Validation of Kits for Aqueous Fluids Aqueous assay validation was performed according to a previously published method by Aydin

, as was briefly described below. Linearity:Two aqueous liquids and blood samples were diluted (1/2,1/4, 1/8) with distilled water in order to find the adiponutrin and pannexin 1 linearity. Recovery: Two aqueous liquids and blood samples were enriched with pure amounts of adiponutrin and pannexin 1. The percentage recovery was calculated as follows: recovered value/expected value ×100. The coefficient of variation

(CV): The intra-assay (within-day) and inter-assay variation (between days) were determined for two different aqueous liquids and blood samples using the means of 2-3 replicates of each. The CV is calculated as: CV=standard deviation (SD)/mean concentration.

The plasma pannexin 1 levels were determined as 2.08±1.17 ng/mL in Group C, 0.98±0.65 ng/mL in Group DM+C, and 1.05±0.91 ng/mL in Group DR+C. The plasma pannexin 1 levels of Groups DM+C and DR+C were statistically significantly lower than those of Group C (both

=0.001) and the difference between Groups DR+C and DM+C was not statistically significant (

=0.417; Figure 2).

The aqueous pannexin 1 levels were determined as 0.69±0.14 ng/mL in Group C, 0.78±0.17 ng/mL in Group DM+C, and 1.54±1.08 ng/mL in Group DR+C. The aqueous pannexin 1 levels of Group DR+C were statistically significantly higher than those of Group C and Group DM+C(

<0.001,

=0.001) and the difference between Groups C and DM+C was not statistically significant (

=0.088; Figure 2).

Adiponutrin and pannexin 1, which play an important role in the pathophysiology of diabetes and obesity, and have a regulatory role in hyperglycemia and insulin resistance. The measurement of adiponutrin and pannexin 1 levels may support clinicians in determining the risk of DR development.

DISCUSSION

上述半定規劃將求解從低維空間轉化到了高維空間,ADM算法獲得的解與真實值之間仍然存在相當的誤差[13,15]。為了……