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Free fatty acids,glucose,and insulin in type 2 diabetes mellitus

2022-10-15 02:53:02RobNMWeijers
World Journal of Diabetes 2022年3期

TO THE EDlTOR

In the August 2021 issue of

,Xu

[1]reported on the association of β-cell function and insulin resistance with pediatric type 2 diabetes among Chinese children.The term "insulin resistance"in the article needs additional clarification and review.

As early as 1933,there was as yet no general agreement as to the definition of the term "insulin resistance" and thus gaps in research and clinical care persisted.The breakthrough of the correct description of the term was a clear example of serendipity.A study by Takematsu

[2]compared genome-wide changes in the gene expression in skin between patients with type 2 diabetes and nondiabetic patients

RNA sequencing,resulting in the identification of 64 significantly upregulated genes and 120 significantly downregulated genes.Among these regulated genes,the most downregulated gene was

,with a down regulation value of 3.7 × 10

,and in the metabolism category the most downregulated gene was

,also with a down regulation value of 3.7 × 10

.The latter gene has not been linked to type 2 diabetes.

They lived together in peace and harmony, although they were very different in character, the man being good-natured and honest, and the wife being greedy and quarrelsome when anyone came her way that she could possibly quarrel with

Defective NKX2-1 production is associated with an essential reduction in the activity of the mitochondrial respiratory chain complex,which reduces ATP production.This idea is supported by the data from a study suggesting that a dysregulation of intramyocellular fatty acid metabolism in the offspring of patients with type 2 diabetes was associated with an inherited defect in mitochondrial oxidative phosphorylation[3].To restore ATP production,the β-oxidation of fatty acids provides assistance by increasing the levels of plasma free fatty acids(FFAs)

hydrolysis.Calculation of the saturation indices(number of cis carbon-carbon double bonds per 100 fatty acyl-chains[4])of FFAs released from human white fat cells and human plasma FFAs in healthy controls reveals that the index of the former is substantially lower(85.5 and 191.9,respectively;Δ = 55.4%)[5].Thus,we can conclude that an increase in the release of FFAs into the blood circulation due to an essential reduction in the activity of the mitochondrial respiratory chain complex leads to a marked reduction in the unsaturated index.

In a previous study,the author found that,in brown adipose tissue,the mitochondrial population exists as two subclasses:cytoplasmic mitochondria that do not adhere to lipid droplets and mitochondria that do adhere to lipid droplets.The lipid droplets are cytosolic storage organelles consisting mostly of neutral lipids and enclosed by a phospholipid monolayer membrane[6].This monolayer has persistent surface packing defects,whereby neutral lipids are accessible to the aqueous cytoplasm and the blood circulation.The idea is that TPD52L3 covers these defects in healthy individuals.Thus,it seems likely that the significant downregulation of

causes an increase in FFAs in the blood circulation and also lowers the saturation index.

Up to now,it has been thought that the glucose-insulin axis is central to the metabolic activities that lead to type 2 diabetes.A publication in 1992 is an exception in this respect,having the title:"What if Minkowski had been ageusic? An alternative angle on diabetes"[9].This study suggested that the basic pathophysiological mechanisms of type 2 diabetes might be more readily understood if viewed in the context of underlying abnormalities of lipid metabolism.Xu

[1]used the HOMA2 model to estimate β-cell function and insulin resistance levels in a pediatric individual from simultaneously measured fasting serum glucose and fasting serum insulin concentrations.The summarized phenomena,in my opinion,are a scientific basis for the idea that membrane flexibility plays an important part in the onset of type 2 diabetes.

Therefore,I suggest that Xu

[1]add to their article a follow-up study including the unsaturation index,as a parameter for membrane flexibility,based on the erythrocyte membrane fatty-acid compositions because,at the most basic level,the basal metabolic rate of a cell is directly linked to its cell membrane's acyl composition[10].A strong argument in favor of the FFA-glucose-insulin axis is the observation that in persons at high risk for type 2 diabetes,the incidence of diabetes was reduced by 58% with lifestyle intervention and by 31% with metformin,as compared with placebo[11].It seems likely that physical activity,after all,raises the levels of the unsaturation index,in contrast to metformin.

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be constructed as a potential conflict of interest.

The Prince, without the smallest hesitation47, snatched up a great stone, and hammered vigorously upon the bell, which gave forth48 a deep and terrible sound, the gate flew open, and closed again with a thundering clang the moment the Prince had passed through it, while from every tower and battlement rose a wheeling, screaming crowd of bats which darkened the whole sky with their multitudes

Thus,we can conclude that the downregulation of

and

forces an increase in the release of FFAs into the blood circulation due to the leaky lipid droplets and the essential reduction in mitochondrial oxidative and phosphorylation activity,and thereby reduces the unsaturation index,as demonstrated in impaired glucose tolerance[7](Table 5 in Weijers[7]),gestational diabetes mellitus[7](Table 5 in Weijers[7]),and type 2 diabetes[4](Table 2 in Weijers[4]).These phenomena lead to a marked shift from unsaturated to saturated acyl chains in the membrane phospholipids,which redistributes the lateral pressure profile of the cell membrane[8].The redistribution of this profile narrows the pore diameter of the transmembrane glucose transport channels of all class I glucose transporter proteins,and thus reduces the rate of transport of glucose molecules across the cell membrane,initiating the onset of type 2 diabetes[7].

FOOTNOTES

Weijers RNM solely contributed to this paper.

The following conclusions can be drawn from the presented information.First,type 2 diabetes is characterized by reduced membrane flexibility in the pancreatic β-cell,which adversely affects the amount of glucose entering the β-cell

GLUT2,and thereby lowers the synthesis of the necessary amount of circulating insulin molecules.Secondly,fusion of the insulin-containing granule with the βcell plasma membrane,followed by the formation of a suitable pore diameter for insulin transport into the blood circulation,requires high flexibility in both the granule-cell membrane and the β-cell membrane.The reduction in the flexibility of both membranes lowers the insulin release from the β-cell into the blood circulation.These facts underline the fact that a reduction in membrane flexibility lowers not only the rate of transport of glucose molecules into the β-cell but also the rate of transport of insulin molecules from the β-cell into the blood circulation.

Rob NM Weijers 0000-0003-2315-6756.

Netherlands

This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers.It is distributed in accordance with the Creative Commons Attribution NonCommercial(CC BYNC 4.0)license,which permits others to distribute,remix,adapt,build upon this work non-commercially,and license their derivative works on different terms,provided the original work is properly cited and the use is noncommercial.See:https://creativecommons.org/Licenses/by-nc/4.0/

43. Not worthy of a king: The mothers in the Princess and the Pea and de Villeneuve s version of Beauty and the Beast are also concerned about the royal heritage and perceived worthiness of their sons wives, although they do not resort to wicked ways to get rid of the prospective brides.Return to place in story.

Zhang H

“Yes, listen,” replied the crow, “but it is so difficult to speak your language. If you understand the crows’ language then I can explain it better. Do you?”

Webster JR

Oh. She licked her fingers, seemingly satisfied with my answer. Then, studying the next marshmallow before she popped it into her mouth, she looked up with the sweetest smile and said softly, We re so lucky that they bloomed today!

Zhang H

1 Xu ZR,Du HW,Cui LW,Zheng RX,Li GM,Wei HY,Lu FY,Chen LL,Wu CS,Zhang SX,Zhang SL,Liu F,Zhang MY,Pei Z,Sun CJ,Wu J,Luo FH.Association of β-cell function and insulin resistance with pediatric type 2 diabetes among Chinese children.

2021;12:1292-1303[PMID:34512894 DOI:10.4239/wjd.v12.i8.1292]

2 Takematsu E,Spencer A,Auster J,Chen PC,Graham A,Martin P,Baker AB.Genome wide analysis of gene expression changes in skin from patients with type 2 diabetes.

2020;15:e0225267[PMID:32084158 DOI:10.1371/journal.pone.0225267]

3 Petersen KF,Dufour S,Befroy D,Garcia R,Shulman GI.Impaired mitochondrial activity in the insulin-resistant offspring of patients with type 2 diabetes.

2004;350:664-671[PMID:14960743 DOI:10.1056/NEJMoa031314]

4 Weijers RNM.Unsaturation index and type 2 diabetes:unknown,unloved.

2015;3:89-92[DOI:10.13105/wjma.v3.i2.89]

5 Weijers RN.Membrane flexibility,free fatty acids,and the onset of vascular and neurological lesions in type 2 diabetes.

2015;15:13[PMID:27123439 DOI:10.1186/s40200-016-0235-9]

6 Weijers RNM.Identification of downregulation of TPD52-Like3 gene and NKX2-1 gene in type 2 diabetes mellitus

RNA sequencing.

2020;3:277-281[DOI:10.32474/ado.2020.03.000156]

7 Weijers RN.Fundamentals about onset and progressive disease character of type 2 diabetes mellitus.

2020;11:165-181[PMID:32477453 DOI:10.4239/wjd.v11.i5.165]

8 Cantor RS.Lateral pressures in cell membranes:a mechanism for modulation of protein function.

1997;101:1723-1725[DOI:10.1021/jp963911x]

9 McGarry JD.What if Minkowski had been ageusic?

1992;258:766-770[PMID:1439783 DOI:10.1126/science.1439783]

10 Hulbert AJ.Life,death and membrane bilayers.

2003;206:2303-2311[PMID:12796449 DOI:10.1242/jeb.00399]

11 Knowler WC,Barrett-Connor E,Fowler SE,Hamman RF,Lachin JM,Walker EA,Nathan DM;Diabetes Prevention Program Research Group.Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin.

2002;346:393-403[PMID:11832527 DOI:10.1056/NEJMoa012512]

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