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   Table of Contents      
LETTER TO THE EDITOR
Year : 2011  |  Volume : 59  |  Issue : 5  |  Page : 403

Inferences from targeting CYP450 modulation to decrease the risk of induced cataract in the experimental model?


1 Department of Ophthalmology, SMIMER, Surat, India
2 Indian Institute of Public Health, Gandhinagar, Gujarat, India

Date of Web Publication9-Aug-2011

Correspondence Address:
Deepak B Saxena
Indian Institute of Public Health, Gandhinagar, Gujarat
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0301-4738.83626

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How to cite this article:
Singhal D, Saxena DB. Inferences from targeting CYP450 modulation to decrease the risk of induced cataract in the experimental model?. Indian J Ophthalmol 2011;59:403

How to cite this URL:
Singhal D, Saxena DB. Inferences from targeting CYP450 modulation to decrease the risk of induced cataract in the experimental model?. Indian J Ophthalmol [serial online] 2011 [cited 2019 Dec 14];59:403. Available from: http://www.ijo.in/text.asp?2011/59/5/403/83626

Dear Editor,

This refers to a well drafted article by Patel et al., published in a recent issue of Indian Journal of Ophthalmology.[1] The present study is based on the hypothesis that basic pathology for cataract is conversion of excess glucose to sorbitol (which can cause cataract) by enzyme aldose reductase using NADPH as a cofactor, and electron transfer from NADPH that depends on the cytochrome P450 system (CYP450). It was postulated that by inducing or inhibiting cytochrome, one can alter the activity of aldose reductase, formation of sorbitol, and hence modulate the occurrence of cataract. The authors have made attempts to prove this by using pioglitazone as CYP450 inducer and nifedipine as CYP450 inhibitor, and used statistical tests to establish the significance.

We would like to draw the attention of the authors on the below-mentioned points:

  1. Use of galactose in the present study in diet fed to the rats for accelerating the process of cataract. In a similar experimental study on rats by Tomlinson, he had opined that rats fed on galactose are not a good model of diabetes and the subsequent induction of cataract. More so, galactose fed animal models lead to a subsequent clinical failure of aldose reductase inhibitors. [2]
  2. Role of pioglitazone in cytochrome modulation is questionable but there are evidences that it has a weak inducer effect on CYP450 inducer; hence, the use of pioglitazone in the present study has made the inferences of the present study doubtful. [3],[4],[5]
  3. Nifedipine was used as an inhibitor in the present study. Liver is the major site for nifedipine metabolism. [6] In addition, as hypothesized that P-glycoprotein (P-gp) is responsible for the large inter-individual difference in CYP3A-mediated drug disposition is not true with nifedipine because it is not a substrate of P-gp. [7] Therefore, nifedipine pharmacokinetics must be crucially determined by total liver CYP3A activities, as nifedipine does not directly modulate the activity of aldose reductase, which is absent in the liver, and where most of the nifedipine is expected to undergo first-pass metabolism. [8] Therefore, some other agent with a better CYP450 inhibitor should have been used.
  4. Finally, to test the association, authors have used analysis of variance (ANOVA) and the post hoc Tukey test, whereas the entire results are expressed as the percentage of total number of lenses affected. Hence, the data set is expressed as nominal data, and thus the 'Chi-square test' could have been a better choice instead of ANOVA in the present condition.


 
  References Top

1.
Patel DV, Gandhi TR, Patel KV, Patil DB, Parikh PV. Targeting CYP450 modulation to decrease the risk of induced cataract in the experimental model. Indian J Ophthalmol 2010;58:471-5.  Back to cited text no. 1
[PUBMED]  Medknow Journal  
2.
Tomlinson DR. Aldose reductase and tissue damage in diabetes. In: Van Bijsternald OP, editor. Diabetic Retinopathy. Houten, The Netherlands: Informa Health Care; 2000. p. 194.  Back to cited text no. 2
    
3.
Ishida T, Hosokawa H, Murao K, Tada T, Taminato T, Taka-Hara J. The effect of troglitazone and pioglitazone on urinary excretion of 6b-hydroxycortisol in steroid induced diabetes. Diabetes 2000;49:115-8.  Back to cited text no. 3
    
4.
Petrie J. Chinese whispers and pioglitazone [Rapid Responses]. BMJ-online 2000.   Back to cited text no. 4
    
5.
Glazer NB. Pioglitazone does not induce cytochrome P450 isoform CYP3A4 [Rapid Responses]. BMJ-online 2000.   Back to cited text no. 5
    
6.
Fukuda T, Onishi S, Fukuen S, Ikenaga Y, Ohno M, Hoshino K, et al. CYP3A5 genotype did not impact on nifedipine disposition in healthy volunteers. Pharmacogenomics J 2004;4:34-9.  Back to cited text no. 6
    
7.
Kim RB, Wandel C, Leake B, Cvetkovic M, Fromm MF, Dempsey PJ. Interrelationship between substrates and inhibitors of human CYP3A and P-glycoprotein. Pharmacol Res 1999;16:408-14.  Back to cited text no. 7
    
8.
Thummel EK, Shen DD, Isoherranen N, Smith HE. Design and optimization of dosage regimen: Pharmacokinetic data. In: Brunton LL, Lazo JS, Parker KL, editors. Goodman and Gilman′s The pharmacological basis of therapeutics. 11 th ed. New York: McGraw-Hill; 2006. p. 1818-60.  Back to cited text no. 8
    




 

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