Study on Moxibustion Improving Reproductive Function of Rats in Cold Stress Model by Activating Hypothalamic Arcuate Nucleus Kisspeptin Neurons to Regulate the Kisspeptin/GPR54 Pathway
Restricted accessResearch articleFirst published online 2026
Study on Moxibustion Improving Reproductive Function of Rats in Cold Stress Model by Activating Hypothalamic Arcuate Nucleus Kisspeptin Neurons to Regulate the Kisspeptin/GPR54 Pathway
Objective: This study examined how moxibustion affects reproductive function, the Kisspeptin/G protein-coupled receptor 54 (GPR54) pathway, and arcuate nucleus (ARC) Kisspeptin neurons in cold-stressed rats. This study explored the mechanisms by which moxibustion enhances reproductive function in cold-stressed rats, through the Kisspeptin/GPR54 pathway, and clarified the role of Kisspeptin neuron activation in the improvement of reproductive function by moxibustion. Methods: A total of 72 female Sprague Dawley rats (SPF, 6–8 weeks, regular estrous cycles) were divided into six groups: blank, cold, moxibustion, TAK488, chemogenetics, and chemogenetics + moxibustion. Cold-stress model was induced through ice-water baths and epinephrine injections. Moxibustion and chemogenetics + moxibustion groups received daily 20 min treatments. The TAK488 group was administered the KISS1R agonist TAK488 subcutaneously every other day for 14 days. Except for the blank and TAK488 groups, the remaining four groups received AAV chemogenetics virus injections into the ARC. Three weeks post-injection, the chemogenetics and chemogenetics + moxibustion groups received intraperitoneal CNO for 14 days. Assessments included cold symptom scores, ovarian histology, ELISA for serum and hypothalamic tissue, immunohistochemistry (IHC), real-time quantitative real-time polymerase chain reaction (qRT-PCR), Western blot, and immunofluorescence (IF) of the hypothalamus or ovary. Results: Compared with the blank group, cold rats showed higher cold symptom scores, decreased serum 6-keto-prostaglandin F1α (6-keto-PGF1α), increased thromboxane B2(TXB2), reduced reproductive hormones [estradiol 2 (E2), follicle-stimulating hormone (FSH), luteinizing hormone (LH), gonadotropin-releasing hormone (GnRH)], and downregulated Kisspeptin/GPR54 pathway factors. Moxibustion lowered cold scores, enhanced blood circulation, elevated reproductive hormones, and activated the Kisspeptin/GPR54 pathway. Kisspeptin neuron activation similarly improved rat condition; elevated serum levels of E2, FSH, and LH reduced levels of dopamine (DA) and neuropeptide Y (NPY); and activated the pathway. The combination of chemogenetics activation and moxibustion yielded superior results. Conclusion: Moxibustion enhances reproductive function by activating ARC Kisspeptin neurons and regulating the Kisspeptin/GPR54 pathway.
BarraR.CruzG.MayerhoferA.ParedesA.LaraH. E. (2014). Maternal sympathetic stress impairs follicular development and puberty of the offspring. Reproduction, 148(2), 137–145. https://doi.org/10.1530/REP-14-0150
2.
BoschE.AlviggiC.LispiM.ConfortiA.HanyalogluA. C.ChuderlandD.SimoniM.Raine-FenningN.CrépieuxP.KolS.RochiraV.D'HoogheT.HumaidanP. (2021). Reduced FSH and LH action: Implications for medically assisted reproduction. Human Reproduction, 36(6), 1469–1480. https://doi.org/10.1093/humrep/deab065
3.
CarrascoR. A.JangJ.JungJ., et al.Prostaglandin synthesis mediates the suppression of arcuate Kiss1 neuron activation and pulsatile luteinizing hormone secretion during immune/inflammatory stress in female mice. Journal of Neuroendocrinology, 37(5), e70004. https://doi.org/10.1111/jne.70004
4.
Cheng, X. M., Du, H. L., Lu, S., et al. (2012). Changes in hypothalamic neurotransmitters in rats with cold-induced blood stasis model and their effects on reproductive endocrinology. Journal of Beijing University of Traditional Chinese Medicine, 35(10), 670–672.
5.
China Association of Acupuncture and Moxibustion. (2025). Nomenclature and location of acupuncture points for laboratory animals part 2: Rat. World Journal of Acupuncture-Moxibustion, 35(2), 163–165. https://doi.org/10.1016/j.wjam.2024.12.003
6.
De BondJ.-A. P.SmithJ. T. (2014). Kisspeptin and energy balance in reproduction. Reproduction (Cambridge, England), 147(3), R53–R63. https://doi.org/10.1530/REP-13-0509
7.
DesroziersE.MikkelsenJ.SimonneauxV.KellerM.TilletY.CaratyA.FranceschiniI. (2010). Mapping of kisspeptin fibres in the brain of the pro-oestrous rat. Journal of Neuroendocrinology, 22(10), 1101–1112. https://doi.org/10.1111/j.1365-2826.2010.02053.x
8.
HanS. Y.McLennanT.CzieselskyK.HerbisonA. E. (2015). Selective optogenetic activation of arcuate kisspeptin neurons generates pulsatile luteinizing hormone secretion. Proceedings of the National Academy of Sciences, 112(42), 13109–13114. https://doi.org/10.1073/pnas.1512243112
9.
HarterC. J. L.KavanaghG. S.SmithJ. T. (2018). The role of kisspeptin neurons in reproduction and metabolism. Journal of Endocrinology, 238(3), R173–r183. https://doi.org/10.1530/joe-18-0108
10.
HesslerS.LiuX.HerbisonA. E. (2020). Direct inhibition of arcuate kisspeptin neurones by neuropeptide Y in the male and female mouse. Journal of Neuroendocrinology, 32(5), e12849. https://doi.org/10.1111/jne.12849
11.
HoffmanG. E.SmithM. S.VerbalisJ. G. (1993). c-Fos and related immediate early gene products as markers of activity in neuroendocrine systems. Frontiers in Neuroendocrinology, 14(3), 173–213. https://doi.org/10.1006/frne.1993.1006
12.
ImaiJ.KatagiriH.YamadaT.IshigakiY.OgiharaT.UnoK.HasegawaY.GaoJ.IshiharaH.SasanoH.OkaY. (2006). Cold exposure suppresses serum adiponectin levels through sympathetic nerve activation in mice. Obesity (Silver Spring), 14(7), 1132–1141. https://doi.org/10.1038/oby.2006.130
13.
KenealyB. P.KeenK. L.GarciaJ. P.RichterD. J.TerasawaE. (2015). Prolonged infusion of estradiol benzoate into the stalk median eminence stimulates release of GnRH and kisspeptin in ovariectomized female rhesus macaques. Endocrinology, 156(5), 1804–1814. https://doi.org/10.1210/en.2014-1979
14.
KhalilZ.LivettB. G.MarleyP. D. (1986). The role of sensory fibres in the rat splanchnic nerve in the regulation of adrenal medullary secretion during stress. The Journal of Physiology, 370, 201–215. https://doi.org/10.1113/jphysiol.1986.sp015930
15.
KimY. K.WasserS. K.FujimotoV. Y.KleinN. A.MooreD. E.SoulesM. R. (1997). Utility of follicle stimulating hormone (FSH), luteinizing hormone (LH), oestradiol and FSH:LH ratio in predicting reproductive age in normal women. Human Reproduction, 12(6), 1152–1155. https://doi.org/10.1093/humrep/12.6.1152
16.
Kinsey-JonesJ. S.LiX. F.KnoxA. M.Kinsey-JonesJ. S.WilkinsonE. S.ZhuX. L.ChaudharyA. A.MilliganS. R.LightmanS. L.O’ByrneK. T. (2009). Down-regulation of hypothalamic kisspeptin and its receptor, Kiss1r, mRNA expression is associated with stress-induced suppression of luteinising hormone secretion in the female rat. Journal of Neuroendocrinology, 21(1), 20–29. https://doi.org/10.1111/j.1365-2826.2008.01807.x
17.
Leka-EmiriS.ChrousosG. P.Kanaka-GantenbeinC. (2017). The mystery of puberty initiation: Genetics and epigenetics of idiopathic central precocious puberty (ICPP). Journal of Endocrinological Investigation, 40(8), 789–802. https://doi.org/10.1007/s40618-017-0627-9
18.
LiX.WangX.ZhouM.LiuJ.SongX.BiK.ChengX. (2025). Wenjing decoction exerts analgesic effects on cold coagulation and stasis PD through BDNF/ TRKB/CREB pathway. Journal of Ethnopharmacology, 352, 120220. https://doi.org/10.1016/j.jep.2025.120220
19.
LinM.ZhangM.-J.FanX.-S., et al. (2023). The skin surface microcirculation of conception vessel, governor vessel and thoroughfare vessel in patients with primary dysmenorrhea. Zhongguo Zhen jiu Chinese Acupuncture & Moxibustion, 43(9), 1042–1047. https://doi.org/10.13703/j.0255-2930.20221227-k0005
20.
LiuJ.YangD.SunX.ZhangY.DengS.DaiH.WuX. (2024). Mass spectrum oriented metabolomics for evaluating the efficacy and discovering the mechanism of Shaofuzhuyu decoction for endometriosis of cold coagulation and blood stasis. Heliyon, 10(13), e33806. https://doi.org/10.1016/j.heliyon.2024.e33806
21.
LiuL.DuanJ. A.TangY.GuoJ.YangN.ShiX. (2012). Taoren-Honghua herb pair and its main components promoting blood circulation through influencing on hemorheology, plasma coagulation and platelet aggregation. Journal of Ethnopharmacology, 139(2), 381–387. https://doi.org/10.1016/j.jep.2011.11.016
22.
LüT.MaX. Y.HuY., et al. (2025). Mechanism of Liangfang Wenjing decoction in regulating endoplasmic reticulum stress to reduce apoptosis and repair ovarian microvascular injury in rats with cold coagulation and blood stasis syndrome. Chinese Journal of Experimental Traditional Medical Formulae, 31(20), 103–114. https://doi.org/10.13422/j.cnki.syfjx.20250809
23.
LvT.HuY.MaX.FengL.WangD.SongX.XueS.ChengX. (2025). Liangfang Wenjing decoction regulates endoplasmic reticulum stress-mediated apoptosis to alleviate uterine microvascular injury in cold-stressed rats. Frontiers in Pharmacology, 16, 1649924. https://doi.org/10.3389/fphar.2025.1649924
24.
MaR.ZhangN.XingJ., et al. (2025). Clinical study on the effects of modified Hupo San on reproductive hormone levels and microcirculation in patients with menstrual disorders of cold congelation and blood stasis pattern. Int J Womens Health, 17, 3271–3278. https://doi.org/10.2147/ijwh.S539135
25.
MacLeanD. B.MatsuiH.SuriA.NeuwirthR.ColombelM. (2014). Sustained exposure to the investigational kisspeptin analog, TAK-448, down-regulates testosterone into the castration range in healthy males and in patients with prostate cancer: Results from two phase 1 studies. The Journal of Clinical Endocrinology & Metabolism, 99(8), E1445–E1453. https://doi.org/10.1210/jc.2013-4236
26.
MasumiS.LeeE. B.DilowerI.UpadhyayaS.ChakravarthiV. P.FieldsP. E.RumiM. A. K. (2022). The role of kisspeptin signaling in oocyte maturation. Frontiers in Endocrinology, 13, 917464. https://doi.org/10.3389/fendo.2022.917464
27.
MatsuiH.MasakiT.AkinagaY.KibaA.TakatsuY.NakataD.TanakaA.BanJ.MatsumotoS.KumanoS.SuzukiA.IkedaY.YamaguchiM.WatanabeT.OhtakiT.KusakaM. (2014a). Pharmacologic profiles of investigational kisspeptin/metastin analogues, TAK-448 and TAK-683, in adult male rats in comparison to the GnRH analogue leuprolide. European Journal of Pharmacology, 735, 77–85. https://doi.org/10.1016/j.ejphar.2014.03.058
28.
MatsuiH.TanakaA.YokoyamaK.MasakiT.AkinagaY.KibaA.TakatsuY.NakataD.BanJ.MatsumotoS.KumanoS.SuzukiA.IkedaY.YamaguchiM.WatanabeT.OhtakiT.KusakaM. (2014b). Chronic administration of the metastin/kisspeptin analog KISS1-305 or the investigational agent TAK-448 suppresses hypothalamic pituitary gonadal function and depletes plasma testosterone in adult male rats. European Journal of Pharmacology, 735(11), 5297–5308. https://doi.org/10.1016/j.ejphar.2014.03.058
29.
MeczekalskiB.NiwczykO.BalaG.SzeligaA. (2022). Stress, kisspeptin, and functional hypothalamic amenorrhea. Current Opinion in Pharmacology, 67, 102288. https://doi.org/10.1016/j.coph.2022.102288
30.
MedinaH.FloresA.Juárez-RojasL.CasillasF.OmmatiM. M.HeidariR.VázquezS.Clavijo-CornejoD.Peña-CoronaS.Retana-MárquezS. (2025). Chronic stress disturbs neuroendocrine control of reproduction and fertility in male rats. Reproductive Biology, 25(3), 101027. https://doi.org/10.1016/j.repbio.2025.101027
31.
NagaeM.UenoyamaY.OkamotoS.TsuchidaH.IkegamiK.GotoT.MajaruneS.NakamuraS.SanboM.HirabayashiM.KobayashiK.InoueN.TsukamuraH. (2021). Direct evidence that KNDy neurons maintain gonadotropin pulses and folliculogenesis as the GnRH pulse generator. Proceedings of the National Academy of Sciences, 118(5). https://doi.org/10.1073/pnas.2009156118
32.
NaorZ. (2009). Signaling by G-protein-coupled receptor (GPCR): Studies on the GnRH receptor. Frontiers in Neuroendocrinology, 30(1), 10–29. https://doi.org/10.1016/j.yfrne.2008.07.001
33.
NaorZ.HuhtaniemiI. (2013). Interactions of the GnRH receptor with heterotrimeric G proteins. Frontiers in Neuroendocrinology, 34(2), 88–94. https://doi.org/10.1016/j.yfrne.2012.11.001
34.
OhtakiT.ShintaniY.HondaS.MatsumotoH.HoriA.KanehashiK.TeraoY.KumanoS.TakatsuY.MasudaY.IshibashiY.WatanabeT.AsadaM.YamadaT.SuenagaM.KitadaC.UsukiS.KurokawaT.NishimuraO.FujinoM. (2001). Metastasis suppressor gene KiSS-1 encodes peptide ligand of a G-protein-coupled receptor. Nature, 411(6837), 613–617. https://doi.org/10.1038/35079135
35.
OrlandoG.LeoneS.FerranteC., et al. (2018). Effects of Kisspeptin-10 on hypothalamic neuropeptides and neurotransmitters involved in appetite control. Molecules, 23(12). https://doi.org/10.3390/molecules23123071
36.
RønnekleivO. K.BoschM. A.ZhangC. (2012). 17β-oestradiol regulation of gonadotrophin-releasing hormone neuronal excitability. Journal of Neuroendocrinology, 24(1), 122–130. https://doi.org/10.1111/j.1365-2826.2011.02160.x
37.
RuohonenS. T.GaytanF.Usseglio GaudiA.VelascoI.KukoriczaK.Perdices-LopezC.FranssenD.GulerI.MehmoodA.EloL. L.OhlssonC.PoutanenM.Tena-SempereM. (2022). Selective loss of kisspeptin signaling in oocytes causes progressive premature ovulatory failure. Human Reproduction, 37(4), 806–821. https://doi.org/10.1093/humrep/deab287
38.
ShenX.LiuY.LiX. F.LongH.WangL.LyuQ.KuangY.O’ByrneK. T. (2022). Optogenetic stimulation of Kiss1(ARC) terminals in the AVPV induces surge-like luteinizing hormone secretion via glutamate release in mice. Front Endocrinol (Lausanne), 13, 1036235. https://doi.org/10.3389/fendo.2022.1036235
39.
SkorupskaiteK.GeorgeJ. T.AndersonR. A. (2014). The kisspeptin-GnRH pathway in human reproductive health and disease. Human Reproduction Update, 20(4), 485–500. https://doi.org/10.1093/humupd/dmu009
40.
SongS.ChenH. (2025). Systematic review and meta-analysis of the effectiveness of moxibustion therapy for primary dysmenorrhea. Frontiers in Medicine, 12, 1545146. https://doi.org/10.3389/fmed.2025.1545146
41.
SuSDuanJCuiW, et al. (2013) Network-based biomarkers for cold coagulation blood stasis syndrome and the therapeutic effects of shaofu zhuyu decoction in rats. Evid Based Complement Alternat Med2013: 901943. https://doi.org/10.1155/2013/901943
42.
SzawkaR. E.RibeiroA. B.LeiteC. M., et al. (2009). Kisspeptin regulates prolactin release through hypothalamic dopaminergic neurons. Endocrinology, 151(7), 3247–3257. https://doi.org/10.1210/en.2009-1414
43.
TaoY.ZhangY.JinX.HuaN.LiuH.QiR.HuangZ.SunY.JiangD.SnutchT. P.JiangX. (2023). Epigenetic regulation of beta-endorphin synthesis in hypothalamic arcuate nucleus neurons modulates neuropathic pain in a rodent pain cold. Nature Communications, 14(1), 7234. https://doi.org/10.1038/s41467-023-43022-7
44.
TapperR.PetterssonH.StjernbrandtA.IkäheimoT. M.WahlströmJ. (2025). Cold exposure among outdoor workers in the Arctic setting. International Journal of Circumpolar Health, 84(1), 2561278. https://doi.org/10.1080/22423982.2025.2561278
45.
Wang, D., Cheng, X. M., Fang, H. M.et al. (2020b). Effects of modified Wenjing decoction on microcirculation in reproductive organs in rats with symptom patterns of cold coagulation and blood stasis. Journal of Traditional Chinese Medical Sciences, 40(2), 212–223.
46.
WangD.ChengX. M.FangH. M., et al. (2020a). Research overview and advances in traditional Chinese medicine treatment for gynaecological cold-induced blood stasis patterns. Journal of Hebei TCM and Pharmacology, 35(01), 60–64. https://doi.org/10.16370/j.cnki.13-1214/r.2020.01.019
47.
WangX.YangX.HangT., et al. (2025). Distribution and characteristics of traditional Chinese medicine syndromes in adenomyosis. Journal of Beijing University of Traditional Chinese Medicine, 48(6). https://doi.org/10.3969/j.issn.1006-2157.2025.06.011
48.
WuL. Y (2023). Acupuncture combined with warm moxibustion box was used to treat primary dysmenorrhea with cold coagulation and blood stasis (Master). Anhui University of Chinese Medicine. https://doi.org/10.26922/d.cnki.ganzc.2023.000454
49.
WuT.DoyleC.ItoJ., et al. (2023). Cold exposures in relation to dysmenorrhea among Asian and White women. Int J Environ Res Public Health, 21(1). https://doi.org/10.3390/ijerph21010056
50.
WuZ.ChenG.QiuC., et al. (2024) Structural basis for the ligand recognition and G protein subtype selectivity of kisspeptin receptor. Science Advances, 10(33), eadn7771. https://doi.org/10.1126/sciadv.adn7771
51.
XieQ.KangY.ZhangC.WangC.LiuJ.YuC.ZhaoH.HuangD. (2022). The role of kisspeptin in the control of the hypothalamic-pituitary-gonadal axis and reproduction. Frontiers in Endocrinology, 13, 925206. https://doi.org/10.3389/fendo.2022.925206
52.
YangJ. M.ShenX. Y.ZhangL., et al. (2014). Evaluation and selection of animal model preparation in cold congealing and blood stasis. China Journal of Chinese Medicine, 29(01), 53–54. https://doi.org/10.16368/j.issn.1674-8999.2014.01.054
53.
ZhangJ.FengY.LiS., et al. (2017). Microvascular pathological features and changes in related injury factors in a rat acute blood stasis model. J Tradit Chin Med, 37(1), 108–115. https://doi.org/10.1016/s0254-6272(17)30034-1
54.
ZhangX.LiuJ.LiX.WangD.SheY.RenY.ChengX. (2025a). Effects of moxibustion at points from the conception, governor, and thoroughfare vessels on hypothalamic-pituitary-ovary axis in rats with cold-induced blood stasis pattern. Journal of Acupuncture and Tuina Science, 23(3), 218–230. https://doi.org/10.1007/s11726-025-1504-2
55.
ZhangX.LiuJ. X.XiaC., et al. (2025b). Exploration on the mechanism of mild moxibustion intervention on gynecological cold coagulation and blood stasis syndrome based on GnRH and its receptor mediated HPO axis. Chinese Journal of Information on Traditional Chinese Medicine, 32(02), 113–119. https://doi.org/10.19879/j.cnki.1005-5304.202406065