Lepidium apetalum.- Northern and Northeastern China Tíng lì zǐ 
Descurainia sophia.
- Eastern and Southern China Tíng lì zǐ.
  Tíng lì zǐ, 独 行 菜 Du xing cai    Pepperweed seed, Lepidium seeds, Descurainia seeds, Woods whitlow grass  Family: Cruciferae    
Tíng lì zǐ is also harvested from Draba nemorosa
PART USED: Seed- harvested in late Summer when the fruit has ripened.
Nature- cold- very cold  FLAVOR: Pungent, bitter.  CHANNEL Lung, Urinary bladder
FUNCTIONS
1. Drain the Lungs, reduce phlegm, and calm wheezing.[1,2,3] Removing Heat from the Lung.
2. Promote urination,[1,2] to reduce edema.[3] Heal swelling.
INDICATIONS
1. Excess type wheeing or coughing with copius sputum and a gurgling sound in the throat due to phlegm accumulation or Lung Heat.[3] Phlegm accumulation and retention manifested as fullness in the chest, cough with dyspnea and profuse sputum, inability to lie flat due to dyspnea, generalized edema.[1,2] Asthma, chest pain, scanty urine, heart disease.[1]
2. Facial edema or fluid accumulation in the chest or abdomen with urinary difficulty due to excess type obstruction of the Lung and Bladder Qi.[3] Pleural effusion, ascites, scanty urination, etc. For water retention in the intestines shown as fullness in the abdomen, dry mouth and tongue.[2]
CONTRAINDICATIONS: Wheezing and cough due to lung Qi deficiency, and for edema due to Spleen deficiency.[3]
PATENT COMBINATIONS
COMBINATIONS
PREPARATIONS: Decoction  Dry ripe seed 3-10 g.[1,3] The seeds are dried in sunlight after collection, used unprepared or stir baked slightly.[2]


References
Inner Path can not take any responsibility for any adverse effects from the use of plants. Always seek advice from a professional before using a plant medicinally.

Constituents

Research

Inhibition of skin pigmentation by an extract of Lepidium apetalum and its possible implication in IL-6 mediated signaling.
Choi H, Ahn S, Lee BG, Chang I, Hwang JS.
Abstract
The development of effective skin-lightening agents is an increasingly important area of research aimed at the treatment of hyperpigmentation induced by UV irradiation or by medical conditions such as melasma, postinflammatory melanoderma and solar lentigo. Although some inhibit tyrosinase, identifying and understanding the mechanisms of action of other agents is an important goal if more effective pigmentation inhibitors are to be developed. We present here that an extract of Lepidium apetalum (ELA) decreased UV-induced skin pigmentation in brown guinea pigs and melanogenesis of HM3KO human melanoma cells. Interestingly, ELA did not reduce melanogenesis in HM3KO cells unless they were co-cultivated in keratinocyte-conditioned medium prepared by culturing keratinocytes with ELA. Under these conditions, ELA decreased tyrosinase mRNA and protein expression as well as melanin content via an ELA-mediated increase in keratinocyte IL-6 production which in turn was shown to decrease in the expression Mitf, a transcription factor implicated in tyrosinase gene expression and melanocyte differentiation. The results reveal that ELA may be an effective inhibitor of hyperpigmentation caused by UV irradiation or by pigmented skin disorders through a mechanism involving IL-6-mediated downregulation of Mitf rather than a direct inhibition of tyrosinase activity.
PMID: 16280009 DOI: 10.1111/j.1600-0749.2005.00266.x  Pigment Cell Res. 2005 Dec;18(6):439-46.  ncbi.nlm.nih.gov

Ethanol Extract of Lepidium apetalum Seed Elicits Contractile Response and Attenuates Atrial Natriuretic Peptide Secretion in Beating Rabbit Atria
Seung Ju Kim, Hye Yoom Kim, Yun Jung Lee, Hao Zhen Cui, Ji Yeon Jang, Dae Gill Kang, and Ho Sub Lee
Abstract
The seeds of Lepidium apetalum Willdenow (called “Tinglizi” in China and “Jungryukza” in Korea) have been used to discharge phlegm and improve dropsy in Oriental medicine. The present study investigated the effects of ethanol extract of the seeds of Lepidium apetalum (ELA) on atrial dynamics and atrial natriuretic peptide (ANP) secretion in beating rabbit atria. ELA increased atrial stroke volume, pulse pressure, and cAMP efflux, concomitantly attenuating ANP secretion in a dose-dependent manner. ELA-induced increases in atrial stroke volume, pulse pressure, and cAMP levels and decrease in ANP secretion were not inhibited by pretreatment with staurosporine, a nonspecific protein kinase inhibitor, or diltiazem and verapamil, the L-type Ca2+ channel blockers, respectively. Helveticoside, a well-known digitalis-like cardiac glycosidic constituent of ELA, also increased atrial dynamics, including stroke volume and pulse pressure, without changing cAMP efflux and ANP secretion, and the effects of helveticoside were not inhibited by pretreatment with staurosporine, diltiazem, and verapamil. These results suggest that the ELA-induced positive inotropic activity in beating rabbit atria might, at least partly, be due to the digitalis-like activity of helveticoside rather than an increase in cAMP efflux.
Journal ListEvid Based Complement Alternat Medv.2013; 2013PMC3830812. Evid Based Complement Alternat Med. 2013; 2013: 404713.
Published online 2013 Oct 29. doi: 10.1155/2013/404713 ncbi.nlm.nih.gov

Bioactive Constituents Obtained from the Seeds of Lepidium apetalum Willd
Sijian Wang, Pingping Shi, Lu Qu, Jingya Ruan, Shengcai Yang, Haiyang Yu, Yi Zhang, Tao Wang
Abstract
Three new compounds, apetalumosides C₁ (1), D (2), and 1-thio--d-glucopyranosyl(1→1)-1-thio-α-d-glucopyranoside (3), together with twenty-two known ones (4-25) were obtained from the seeds of Lepidium apetalum Willd. Among the known isolates, 5-8, 10-13, 16-20, and 25 were obtained from the genus for the first time; 4, 14, 15, and 21-24 were isolated from the species for the first time. Meanwhile, the NMR data of 16 was first reported here. Their structures were determined by means of chemical and spectroscopic methods. On the other hand, their inhibitory effects on sodium oleate-induced triglyceride (TG) overloading in HepG2 cells were evaluated. As a result, two new compounds (1 and 2), together with known isolates 7-11, 13, 14, 16-18, 20, 21, and 25 possessed significant inhibitory effects in the cells.
Molecules 2017 Mar 28;22(4):540. doi: 10.3390/molecules22040540. PMID: 28350346 PMCID: PMC6154599 DOI: 10.3390/molecules22040540 pubmed.ncbi.nlm.nih.gov

Uridine derivatives from the seeds of Lepidium apetalum Willd. and their estrogenic effects
Meng Li, Mengnan Zeng, Zhiguang Zhang, Jingke Zhang, Beibei Zhang, Xuan Zhao, Xiaoke Zheng, Weisheng Feng
Affiliations expand
PMID: 30075391 DOI: 10.1016/j.phytochem.2018.07.013
Abstract
Ten uridine derivatives (lepidiumuridine B-K) were isolated from the seeds of Lepidium apetalum Willd. Lepidiumuridine B-J were previously undescribed compounds, and were structurally characterized using analysis of their NMR and MS data. Lepidiumuridine C, D, I, and J increased cell proliferation and expression of ERα in the MCF-7 cell line. In addition, blockage of ERα completely abolished cell proliferation and expression of ERα in MCF-7 cells, suggesting that the proliferation effects of lepidiumuridine C, D, I, and J were ERα-mediated. The uridine derivatives might belong to undescribed phytoestrogens.
Phytochemistry 2018 Nov;155:45-52. doi: 10.1016/j.phytochem.2018.07.013. Epub 2018 Jul 31. pubmed.ncbi.nlm.nih.gov