Abstract

Polycystic ovary syndrome (PCOS) is the most common endocrine disorder among women of reproductive age. It is a heterogeneous condition characterized by reproductive, endocrine, metabolic, and psychiatric abnormalities. More than one pathogenic mechanism is involved in its development. On the other hand, the hypothalamus plays a crucial role in many important functions of the body, including weight balance, food intake, and reproduction. A high-fat diet with a large amount of long-chain saturated fatty acids can induce inflammation in the hypothalamus. Hypothalamic neurons can sense extracellular glucose concentrations and participate, with a feedback mechanism, in the regulation of whole-body glucose homeostasis. When consumed nutrients are rich in fat and sugar, and these regulatory mechanisms can trigger inflammatory pathways resulting in hypothalamic inflammation. The latter has been correlated with metabolic diseases, obesity, and depression. In this review, we explore whether the pattern and the expansion of hypothalamic inflammation, as a result of a high-fat and -sugar diet, may contribute to the heterogeneity of the clinical, hormonal, and metabolic presentation in PCOS via pathophysiologic mechanisms affecting specific areas of the hypothalamus. These mechanisms could be potential targets for the development of effective therapies for the treatment of PCOS.

Highlights

  • The hypothalamus, being part of diencephalon, is situated beneath the thalamus and above the midbrain

  • Th ity of Gonadotropin-releasing hormone (GnRH) neuronal cell bodies are located in the arcuate nucleususanpodpiunlattihoen mofehdyipaolthparleaompictinceaurroenas.,GwnhRicHh coisntsreocl rreepterdodiunctaionp.ulsatile Tmaheneddmio, batajhosrraioltyuhygopfhoGtthnhaRelHapmnouersut)raaolnndcailirncceutlhlleabmtoidoeidneis,alasrpteirmelooucpatlitacetdaersienas.tyhGnentaRhrHceusiaisstesaencnuredctleesduesicnr(peaatpirout lonsfaotthifleeluteiniz fmashoinone a(nLdH, th)roaungdh tfhoellpiocrltealsctirimculualtaiotnin, sgtimhuolramtesosnyenth(eFsSisHan) dfrsoecmretitohneofalnutteeirniiozirngpituitar hTohrmesoeneg(oLnHa)daontdrofoplliinclse astriemruelastpinognhsoibrmleofnoer(FtShHe)sferocmrethioenanotefrgioornpaitduaitlarsytegrloanidds. , which Tnheegseatgiovneadfeoetrdobpaincskairne rtehsepobnrsaibinle [f3or].the secretion of gonadal steroids, which exert a negative feedback in the brain [3]

  • We explored whether hypothalamic inflammation could represent a common pathophysiologic basis for the heterogeneous clinical, hormonal, and metabolic presentation of Polycystic ovary syndrome (PCOS)

Read more

Summary

Introduction

The hypothalamus, being part of diencephalon, is situated beneath the thalamus and above the midbrain. Dorsomedial, ventromedial, and arcuate (infundibular) nuclei are involved in regulation of body-weight balance, food intake, satiety, thirst, and circadian rhythms. Dysfunction of these nuclei causes hyperphagia and obesity [2]. Gonadotropin-releasing hormone (GnRH) neurons medial, and arcuate (infundibular) nuclei are involved in regulation of body-we ance, food intake, satiety, thirst, and circadian rhythms. Dysfunction of these nucle hyperphagia and obesity [2]. Th ity of GnRH neuronal cell bodies are located in the arcuate nucleus (part of the me ahreypa ohtehtearloagmenueso)usanpodpiunlattihoen mofehdyipaolthparleaompictinceaurroenas.,GwnhRicHh coisntsreocl rreepterdodiunctaionp.ulsatile Tmaheneddmio, batajhosrraioltyuhygopfhoGtthnhaRelHapmnouersut)raaolnndcailirncceutlhlleabmtoidoeidneis,alasrpteirmelooucpatlitacetdaersienas.tyhGnentaRhrHceusiaisstesaencnuredctleesduesicnr(peaatpirout lonsfaotthifleeluteiniz fmashoinone a(nLdH, th)roaungdh tfhoellpiocrltealsctirimculualtaiotnin, sgtimhuolramtesosnyenth(eFsSisHan) dfrsoecmretitohneofalnutteeirniiozirngpituitar hTohrmesoeneg(oLnHa)daontdrofoplliinclse astriemruelastpinognhsoibrmleofnoer(FtShHe)sferocmrethioenanotefrgioornpaitduaitlarsytegrloanidds. , which Tnheegseatgiovneadfeoetrdobpaincskairne rtehsepobnrsaibinle [f3or].the secretion of gonadal steroids, which exert a negative feedback in the brain [3]

Methods
Findings
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call