Gender-Specific Protection of Estrogen against Gastric Acid-Induced Duodenal Injury: Stimulation of Duodenal Mucosal Bicarbonate Secretion

Author:

Smith Anders1,Contreras Cheyanne1,Ko Kwang Hyun1,Chow Jimmy1,Dong Xiao1,Tuo Biguang2,Zhang Hong-hai3,Chen Dong-bao3,Dong Hui1

Affiliation:

1. Departments of Medicine (A.S., C.C., K.H.K., J.C., X.D., H.D.), School of Medicine, University of California San Diego, La Jolla, California 92093

2. Department of Gastroenterology (B.T.), Zunyi Medical College, Zunyi, Guizhou 563003, People’s Republic of China

3. Reproductive Medicine (H.-h.Z., D.-b.C.), School of Medicine, University of California San Diego, La Jolla, California 92093

Abstract

Because human duodenal mucosal bicarbonate secretion (DMBS) protects duodenum against acid-peptic injury, we hypothesize that estrogen stimulates DMBS, thereby attributing to the clinically observed lower incidence of duodenal ulcer in premenopausal women than the age-matched men. We found that basal and acid-stimulated DMBS responses were 1.5 and 2.4-fold higher in female than male mice in vivo, respectively. Acid-stimulated DMBS in both genders was abolished by ICI 182,780 and tamoxifen. Estradiol-17β (E2) and the selective estrogen receptor (ER) agonists of ERα [1,3,5-Tris(4-hydroxyphenyl)-4-propyl-1H-pyrazole] and ERβ [2,3-bis(4-hydroxyphenyl) propionitrile], but not progesterone, rapidly stimulated ER-dependent murine DMBS in vivo. E2 dose dependently stimulated murine DMBS, which was attenuated by a Cl−/HCO3− anion exchanger inhibitor 4,4′-didsothio- cyanostilbene-2, 2′-disulfonic acid, removal of extracellular Cl−, and in cystic fibrosis transmembrane conductance regulator knockout female mice. E2 stimulated murine DMBS in vitro in both genders with significantly greater response in female than male mice (female to male ratio = 4.3). ERα and ERβ mRNAs and proteins were detected in murine duodenal epithelium of both genders; however, neither ERα nor ERβ mRNA and protein expression levels differed according to gender. E2 rapidly mobilized intracellular calcium in a duodenal epithelial SCBN cell line that expresses ERα and ERβ, whereas BAPTA-AM abolished E2-stimulated murine DMBS. Thus, our data show that E2 stimulates DMBS via ER dependent mechanisms linked to intracellular calcium, cystic fibrosis transmembrane conductance regulator, and Cl−/HCO3− anion exchanger. Gender-associated differences in basal, acid- and E2-stimulated DMBS may have offered a reasonable explanation for the clinically observed lower incidence of duodenal ulcer in premenopausal women than age-matched men.

Publisher

The Endocrine Society

Subject

Endocrinology

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