2005
DOI: 10.17305/bjbms.2005.3272
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Serum and tissue angiotensin converting enzyme in patients with lichen planus

Abstract: Serum and tissue angiotensin-converting enzyme (ACE) was measured in 20 patients with lichen planus before and after therapy, and in 20 healthy individuals. Serum and tissue ACE activity was determined by spectrophotometric method using hippuryl-l-histidyl-l-leucine as a substrate. The enzyme activity is expressed in the following units: 1 U corresponds to 1 nmol of hippuric acid released by hydrolysis of hippuryl-l-histidyl-l-leucine per minute and one liter of serum or 50 mg tissue. Before therapy, serum ACE… Show more

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Cited by 5 publications
(4 citation statements)
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“…After therapy, serum and tissue ACE activity decreased and no significant difference in ACE activity was found. 9 Robati et al conducted a study of serum ACE levels in pemphigus in which 34 patients with pemphigus vulgaris and 35 healthy individuals were recruited. The mean serum ACE levels in patients and control groups were 25.34±14.25 and 31.97±19.44 respectively.…”
Section: Discussionmentioning
confidence: 99%
“…After therapy, serum and tissue ACE activity decreased and no significant difference in ACE activity was found. 9 Robati et al conducted a study of serum ACE levels in pemphigus in which 34 patients with pemphigus vulgaris and 35 healthy individuals were recruited. The mean serum ACE levels in patients and control groups were 25.34±14.25 and 31.97±19.44 respectively.…”
Section: Discussionmentioning
confidence: 99%
“…There have been reported two cases suggesting that Captopril and Ramipril induced LP pemphigoides. Unfortunately, mechanisms are still unknown [131][132][133].…”
Section: Lichen Planus (Lp)mentioning
confidence: 99%
“…These findings suggest that angiotensin II may contribute to oral LP through activating TRPA1. Given that circulating angiotensin-converting enzyme (the enzyme the produces angiotensin II) was upregulated in LP patients (Alendar et al, 2005), TRPA1 would be activated and upregulated in both lesion sites and non-lesion sites. However, unfortunately, this study (Kun et al, 2016) did not examine the expression levels of TRPA1 in non-lesion sites.…”
Section: Dear Editormentioning
confidence: 99%