Role of peripheral 5-HT5A receptors in 5-HT-induced cardiac sympatho-inhibition in type 1 diabetic rats
5-HT inhibits cardiac sympathetic neurotransmission in normoglycaemic rats, via 5-HT 1B , 5-HT 1D and 5-HT 5A receptor activation. Since type 1 diabetes impairs the cardiac sympathetic innervation leading to cardiopathies, this study aimed to investigate whether the serotonergic influence on cardiac...
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Veröffentlicht in: | Scientific reports 2020-11, Vol.10 (1), Article 19358 |
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Sprache: | eng |
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Zusammenfassung: | 5-HT inhibits cardiac sympathetic neurotransmission in normoglycaemic rats, via 5-HT
1B
, 5-HT
1D
and 5-HT
5A
receptor activation. Since type 1 diabetes impairs the cardiac sympathetic innervation leading to cardiopathies, this study aimed to investigate whether the serotonergic influence on cardiac noradrenergic control is altered in type 1 diabetic rats. Diabetes was induced in male Wistar rats by streptozotocin (50 mg/kg, i.p.). Four weeks later, the rats were anaesthetized, pithed and prepared for producing tachycardic responses by electrical preganglionic stimulation (C
7
-T
1
) of the cardioaccelerator sympathetic outflow or i.v. noradrenaline bolus injections. Immunohistochemistry was performed to study 5-HT
1B
, 5-HT
1D
and 5-HT
5A
receptor expression in the stellate ganglion from normoglycaemic and diabetic rats. In the diabetic group, i) i.v. continuous infusions of 5-HT induced a cardiac sympatho-inhibition that was mimicked by the 5-HT
1/5A
agonist 5-carboxamidotryptamine (without modifying noradrenaline-induced tachycardia), but not by the agonists indorenate (5-HT
1A
), CP 93,129 (5-HT
1B
), PNU 142633 (5-HT
1D
), or LY344864 (5-HT
1F
); ii) SB 699551 (5-HT
5A
antagonist; i.v.) completely reversed 5-CT-induced cardiac sympatho-inhibition; and iii) 5-HT
5A
receptors were more expressed in the stellate ganglion compared to normoglycaemic rats. These results show the prominent role of the peripheral 5-HT
5A
receptors prejunctionally inhibiting the cardiac sympathetic drive in type 1 diabetic rats. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-020-76298-6 |