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Placenta Encapsulation

The Facts

"During a normal vaginal delivery a new mother will lose at least one eighth to one tenth of her body’s blood supply, with cesarean section births blood loss can be significantly more. Losing a large amount iron so quickly can cause anemia, leaving a new mum feeling tired, faint and exhausted. The blood needs high supplies of iron to carry oxygen to the cells – low supplies of oxygen leave your cells starving and less able to heal after trauma. The placenta benefits the new mother by supplying incredibly rich iron, amino acids and essential fats which we believe is the be the perfect replenishment following birth.
 
The most important nutrients found in rich supply in the placenta include:
Iron – essential for oxygen absorbtion in the cellsvitamins B6 – aids in the making of antibodies
Vitamin E – for healing damaged skin cellsOxytocin hormone – essential for facilitating birth and breastfeeding
Corticotropin-releasing hormone (CRH) – responsible for reducing stress levels
Cytokins – Fibroblasts that trigger cell metabolism healing and replacing damaged cells and tissue
 
The placenta benefits a healing mother after birth in many forms. Capsules, tinctures, essences, and homeopathic remedies can all be made using the placenta; each having their own benefit to the body and encouraging a quicker more natural recovery after birth.” (IPEN) Click here to read an article on placenta encapsulation in Green Parent.

 

RESEARCH

 

Placenta Increases Milk Production

Placenta as Lactagagon Soykova-Pachnerova E, et. al.(1954). Gynaecologia 138(6):617-627. An attempt was made to increase milk secretion in mothers by administration of dried placenta per os. Of 210 controlled cases only 29 (13.8%) gave negative results; 181 women (86.2%) reacted positively to the treatment, 117 (55.7%) with good and 64 (30.5%) with very good results. It could be shown by similar experiments with a beef preparation that the effective substance in placenta is not protein. Nor does the lyofilised placenta act as a biogenic stimulator so that the good results of placenta administration cannot be explained as a form of tissue therapy per os. The question of a hormonal influence remains open. So far it could be shown that progesterone is probably not active in increasing lactation after administration of dried placenta. This method of treating hypogalactia seems worth noting since the placenta preparation is easily obtained, has not so far been utilized and in our experience is successful in the majority of women.

 

Placentophagia: A Biobehavioral Enigma

Placentophagia: A Biobehavioral Enigma KRISTAL, M. B. NEUROSCI. BIOBEHAV. REV. 4(2) 141-150, 1980. Although ingestion of the afterbirth during delivery is a reliable component of parturitional behavior of mothers in most mammalian species, we know almost nothing of the direct causes or consequences of the act. Traditional explanations of placentophagia, such as general or specific hunger, are discussed and evaluated in light of recent experimental results. Next, research is reviewed which has attempted to distinguish between placentophagia as a maternal behavior and placentophagia as an ingestive behavior. Finally, consequences of the behavior, which may also be viewed as ultimate causes in an evolutionary sense, are considered, such as the possibility of beneficial effects on maternal behavior or reproductive competence, on protection against predators, and on immunological protection afforded either the mother or the young.

 

Placenta ingestion for pain relief

Placenta for Pain Relief: Placenta ingestion by rats enhances y- and n-opioid antinociception, but suppresses A-opioid antinociception Jean M. DiPirro*, Mark B. Kristal Ingestion of placenta or amniotic fluid produces a dramatic enhancement of centrally mediated opioid antinociception in the rat. The present experiments investigated the role of each opioid receptor type (A, y, n) in the antinociception-modulating effects of Placental Opioid-Enhancing Factor (POEF—presumably the active substance). Antinociception was measured on a 52 jC hotplate in adult, female rats after they ingested placenta or control substance (1.0 g) and after they received an intracerebroventricular injection of a y-specific ([D-Pen2,D-Pen5]enkephalin (DPDPE); 0, 30, 50, 62, or 70 nmol), A-specific ([D-Ala2,N-MePhe4,Gly5-ol]enkephalin (DAMGO); 0, 0.21, 0.29, or 0.39 nmol), or n-specific (U-62066; spiradoline; 0, 100, 150, or 200 nmol) opioid receptor agonist. The results showed that ingestion of placenta potentiated y- and n-opioid antinociception, but attenuated A-opioid antinociception. This finding of POEF action as both opioid receptor-specific and complex provides an important basis for understanding the intrinsic pain-suppression mechanisms that are activated during parturition and modified by placentophagia, and important information for the possible use of POEF as an adjunct to opioids in pain management. D 2004 Elsevier B.V. All rights reserved.

 

Placentophagy alters hormone levels

Effects of placentophagy on serum prolactin and progesterone concentrations in rats after parturition or superovulation. Blank MS, Friesen HG.: J Reprod Fertil. 1980 Nov;60(2):273-8. In rats that were allowed to eat the placentae after parturition concentrations of serum prolactin were elevated on Day 1 but concentrations of serum progesterone were depressed on Days 6 and 8 post partum when compared to those of rats prevented from eating the placentae. In rats treated with PMSG to induce superovulation serum prolactin and progesterone values were significantly (P < 0.05) elevated on Days 3 and 5 respectively, after being fed 2 g rat placenta/day for 2 days. However, feeding each rat 4 g placenta/day significantly (P < 0.02) lowered serum progesterone on Day 5. Oestrogen injections or bovine or human placenta in the diet had no effect. The organic phase of a petroleum ether extract of rat placenta (2 g-equivalents/day) lowered peripheral concentrations of progesterone on Day 5, but other extracts were ineffective. We conclude that the rat placenta contains orally-active substance(s) which modify blood levels of pituitary and ovarian hormones.

 

 

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