No abstract

Using a whole-nerve recording method, the genitalia of the female rat were found to receive afferent innervation as follows. Pelvic nerve: vagina, cervix, and perineal skin; hypogastric nerve: cervix and proximal three fifths of the uterus; pudendal nerve: skin of perineum, inner thigh, and clitoral sheath. It is probable that the pudendal and pelvic nerves are activated during copulation, and that all 3 nerves are activated during parturition.

Afterbirth ingestion by nonhuman mammalian mothers has a number of benefits: (1) increasing the interaction between the mother and infant; (2) potentiating pregnancy-mediated analgesia in the delivering mother; (3) potentiating maternal brain opioid circuits that facilitate the onset of caretaking behavior; and (4) suppressing postpartum pseudopregnancy. Childbirth is fraught with additional problems for which there are no practical nonhuman animal models: postpartum depression, failure to bond, hostility toward infants. Ingested afterbirth may contain components that ameliorate these problems, but the issue has not been tested empirically. The results of such studies, if positive, will be medically relevant. If negative, speculations and recommendations will persist, as it is not possible to prove the negative. A more challenging anthropological question is "why don't humans engage in placentophagia as a biological imperative?" Is it possible that there is more adaptive advantage in not doing so?

No abstract

Analgesia, produced by either a morphine injection or footshock, was monitored (using a tail-flick test) in nonpregnant female rats. Analgesia was induced within minutes of having the rats eat one of several substances. When the substance eaten was rat placenta, both the morphine- and shock-induced types of analgesia were significantly greater than in controls that ingested other substances (or nothing). When footshock (hind-paw) was administered in conjunction with the opiate antagonist naltrexone, the analgesia produced was attenuated but detectable; in this case, placenta ingestion did not enhance the analgesia, suggesting that the effect of placenta is specific to opiate-mediated analgesia. Placenta ingestion, in the absence of an analgesia-producing manipulation, did not elevate pain threshold. It is possible that this enhancement of analgesia is one of the principal benefits to mammalian mothers of ingesting the placenta and birth fluids (placentophagia) at delivery.