Evidence map›Paper›PMID 42166028›Full record

ArticleOdontology2026

Changes of salivary secretion after pilocarpine administration twice in a mouse model of Sjögren's syndrome.

Takeyuki Itagaki, Haruka Yamaguchi, Akihiro Nezu, Akihiko Tanimura, Takao Morita

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Article in Odontology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Takeyuki ItagakiMolecular Biology of Saliva and Salivary Glands, Graduate School of Life Dentistry at Niigata, The Nippon Dental University, 1-8 Hamaura-Cho, Chuo- Ku, Niigata, 951-8580, Japan.
Haruka YamaguchiMolecular Biology of Saliva and Salivary Glands, Graduate School of Life Dentistry at Niigata, The Nippon Dental University, 1-8 Hamaura-Cho, Chuo- Ku, Niigata, 951-8580, Japan.
Akihiro NezuDivision of Pharmacology, Department of Oral Biology, School of Dentistry, Health Sciences University of Hokkaido, 1757 Kanazawa, Ishikari- Tobetsu, Hokkaido, 061-0293, Japan.
Akihiko TanimuraDivision of Pharmacology, Department of Oral Biology, School of Dentistry, Health Sciences University of Hokkaido, 1757 Kanazawa, Ishikari- Tobetsu, Hokkaido, 061-0293, Japan.
Takao MoritaMolecular Biology of Saliva and Salivary Glands, Graduate School of Life Dentistry at Niigata, The Nippon Dental University, 1-8 Hamaura-Cho, Chuo- Ku, Niigata, 951-8580, Japan. moritat@ngt.ndu.ac.jp.ORCID http://orcid.org/0009-0003-0331-403X

Funding

JSPI kakenhi 25K12961JSPS kakenhi JSPS KAKENHI Grant Numbers 21K09821
6 · The paper itself

Abstract

Sjögren's syndrome (SS) is an autoimmune disease characterized by dysfunction of exocrine glands. Pilocarpine is used as a symptomatic treatment for xerostomia, and chronic administration has been shown to increase salivary secretion; however, the underlying molecular mechanisms remain unclear. This study examined the effects of pilocarpine administration twice on salivary gland function in non-obese diabetic (NOD) mice, an animal model of SS. Pilocarpine was administered to 16-week-old NOD and wild-type (ICR) mice once a week for 2 weeks, and saliva was collected. Salivary volume, amylase activity, and the expression of aquaporin-5 (AQP5), connective tissue growth factor (Ctgf), and serum-and glucocorticoid-regulated kinase-1 (Sgk1) were examined. The salivary volume in ICR mice was significantly increased following the second administration, but not in NOD mice. No significant differences were observed in the total salivary amylase activity in either ICR or NOD mice. Western blot analysis demonstrated higher AQP5 expression in the membrane fractions and significantly lower expression in the cytosolic fractions of the submandibular glands following pilocarpine administration twice in both ICR and NOD mice, although the total AQP5 protein expression levels did not differ between the two types of mice. Gene expression analysis showed that Ctgf and Sgk1 were significantly upregulated in ICR mice following pilocarpine administration twice, but not in NOD mice. These findings suggest that the mechanism underlying the enhanced gene expression of Ctgf and Sgk1 following pilocarpine administration twice is impaired in NOD mice and that the expression of these genes may be associated with pilocarpine-induced salivary secretion.

Indexed as

gene expressionnon-obese diabetic micepilocarpinesalivary secretionSjögren’s syndrome

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.